Zinc in innate and adaptive tumor immunity
© John et al; licensee BioMed Central Ltd. 2010
Received: 11 June 2010
Accepted: 18 November 2010
Published: 18 November 2010
Zinc is important. It is the second most abundant trace metal with 2-4 grams in humans. It is an essential trace element, critical for cell growth, development and differentiation, DNA synthesis, RNA transcription, cell division, and cell activation. Zinc deficiency has adverse consequences during embryogenesis and early childhood development, particularly on immune functioning. It is essential in members of all enzyme classes, including over 300 signaling molecules and transcription factors. Free zinc in immune and tumor cells is regulated by 14 distinct zinc importers (ZIP) and transporters (ZNT1-8). Zinc depletion induces cell death via apoptosis (or necrosis if apoptotic pathways are blocked) while sufficient zinc levels allows maintenance of autophagy. Cancer cells have upregulated zinc importers, and frequently increased zinc levels, which allow them to survive. Based on this novel synthesis, approaches which locally regulate zinc levels to promote survival of immune cells and/or induce tumor apoptosis are in order.
"Finding a potent role for zinc in the regulation of autophagic PCD establishes zinc deprivation as a universal cell death signal, regardless of which route of degradation--apoptotic or autophagic --is chosen by cells." Andreas Helmersson, Sara von Arnold, and Peter V. Bozhkov. The Level of Free Intracellular Zinc Mediates Programmed Cell Death/Cell Survival Decisions in Plant Embryos. Plant Physiol. 2008 July; 147 (3): 1158-1167.
"It's a business. If I could make more money down in the zinc mines I'd be mining zinc." Roger Maris (American professional Baseball Player. 1934-1985)
"We have everything but the kits in zinc." Albert Donnenberg, PhD (Flow Cytometrist, UPSHS) 2009
Biological Role of Zinc
Zinc is the second most abundant metal in organisms (second only to iron), with 2-4 grams distributed throughout the human body. Most zinc is found in the brain, muscle, bones, kidney, and liver, with the highest concentrations in the prostate and parts of the eye. It is the only metal that is a coenzyme to all enzyme classes [1–3]. A biologically critical role for zinc was first reported in 1869, when it was shown to be required for the growth of the fungus, Aspergillus niger . In 1926, zinc was found to be required for the growth of plants , and shortly thereafter, its first function in animals was demonstrated [6–8]. Now, zinc has been shown to be important also in prokaryotes . In the last half-century the consequences of zinc deficiency have been recognized.
Zinc is a biologically essential trace element; critical for cell growth, development and differentiation . It is required for DNA synthesis, RNA transcription, cell division, and cell activation , and is an essential structural component of many proteins, including signaling enzymes and transcription factors. Zinc is required for the activity of more than 300 enzymes, interacting with zinc-binding domains such as zinc fingers, RING fingers, and LIM domains [12–14]. The RING finger domain is a zinc finger which contains a Cys3HisCys4 amino acid motif, binding two zincs, contains from 40 to 60 amino acids. RING is an acronym specifying Really Interesting New Gene. LIM domains are structural domains, composed of two zinc finger domains, separated by a two-amino acid residue hydrophobic linker. They were named following their discovery in the proteins Lin11, Isl-1 and Mec-3. LIM-domain proteins play roles in cytoskeletal organization, organ development and oncogenesis. More than 2000 transcription factors have structural requirements for zinc to bind DNA, thereby revealing a critical role for zinc in gene expression.
Zinc is required for both normal cell survival (as above) and for cell death via its role in apoptosis. We propose that zinc may also regulate autophagy and other forms of survival due to its early sensitivity to cell stress. Thus, zinc could play a central role, regulating apoptosis and autophagy as well as immune cell function. Cancer cells are continuously stressed (genomic stress, ER stress, nutrient stress, oxidant stress, etc) and selected for survival (likely by autophagy). Here we review the current studies surrounding zinc, and propose that zinc has a spectrum of effects on cell death and survival, where zinc depletion induces cell death via apoptosis (or necrosis if apoptotic pathways are blocked) while sufficient zinc levels allows maintenance of cell survival pathways such as autophagy and regulation of reactive oxygen species. Cancer cells have upregulated zinc importers, and most frequently increased zinc levels, which allow them to survive. Based on these notions, means to locally regulate zinc levels to promote survival of immune cells and promote tumor apoptosis are in order.
Dietary Zinc and Deficiency
Red meat is the primary sources of zinc for most Americans. The already low amount of zinc in vegetables is further chelated by phytates and is therefore not as available for absorption. Nuts, and fruits, whole grain bread, dairy products, and fortified breakfast cereals are other sources of zinc. Oysters have the highest zinc per serving of any common food [15, 16].
Zinc is taken up primarily in the proximal small intestine, and depends heavily on ZIP4. Once transported through the enterocytes and into the blood, zinc binds to albumin, transferrin, α-2 macroglobulin, and immunoglobulin G, and travels to the liver where the zinc is stored in hepatocytes until it is released back into the blood to again bind carrier molecules and travel to the tissues where zinc intake will be regulated by zinc import and transport proteins .
Over one billion people in developing countries are nutritionally deficient in zinc . Zinc deficiency is associated with a range of pathological states, including skin changes, loss of hair, slowed growth, delayed wound healing, hypogonadism, impaired immunity, and brain development disorders [6, 10, 19], all of which are reversible with zinc supplementation. Zinc deficiencies occur as a result of malabsorption syndromes and other gastrointestinal disorders, chronic liver and renal diseases, sickle cell disease, excessive alcohol intake, malignancy, cystic fibrosis, pancreatic insufficiency, rheumatoid arthritis, and other chronic conditions [18, 20–25]. In humans, acrodermatitis enteropathica-like eruptions are commonly found with zinc deficiency . These pathological states and the associated zinc deficiencies are linked to increased infection and prolonged healing time, both of which are indicators of compromised immunity. In developing countries, previously pervasive conditions such as diarrhea  and lower respiratory illness  are associated with low zinc. Unfortunately, quantifying human zinc to identify deficiency and preventing zinc toxicity (due to excess supplementation) is an ongoing challenge . These findings suggest a role for zinc in immune cell homeostasis in vivo[30, 31].
A Signaling Ion
Zinc may act as a signaling molecule, both extracellularly (as in neurotransmitters) and intracellularly (as in calcium second-messenger systems). In nerve cells, zinc can be found in membrane-enclosed synaptic vesicles, from which it is released via exocytosis to bind ligand gated ion channels (such as NMDA receptors, Ca2+-permeable AMPA/kainite receptors, and voltage-dependent Ca2+ channels (VDCC)), activating postsynaptic cells . Additionally, changes in the concentration of intracellular free zinc control immune cell signal transduction by regulating the activity of major signaling molecules, including kinases (PKC, LCK), phosphatases (cyclic nucleotide phosphodiesterases and MAPK phosphatases), and transcription factors (NFkB).
In T cells, zinc treatment stimulates the kinase activity of PKC, its affinity to phorbol esters, and its binding to the plasma membrane and cytoskeleton , while zinc chelators inhibit the induction of these events . Zinc ions also promote activation of LCK, a Src-family tyrosine kinase, and its recruitment to the T cell receptor complex . The interaction of LCK with CD44 is also zinc dependent . The release of zinc from lysosomes also appears to promote T-cell proliferation in response to IL-2R activation. Here, zinc causes its effect through the ERK pathway, possibly by inhibiting the dephosphorylation of MEK and ERK . Additionally, zinc regulates inflammatory signaling in monocytes treated with lipopolysaccharide (LPS), interacting with cyclic nucleotide phosphodiesterases and MAPK phosphatases [38–40]. NFkB is a transcription factor involved in cellular responses to stressful stimuli including cytokines, free radicals, ultraviolet irradiation, oxidized LDL, and bacterial or viral infection that plays a key role in regulating the immune response . Zinc regulates upstream signaling pathways leading to the activation of this transcription factor , as well as potentially regulating NFkB itself . Interestingly, peripheral blood mononuclear cells (PBMC) from zinc-deficient elderly individuals show impaired NFkB activation and diminished interleukin (IL-2) production in response to stimulation with the mitogen phytohemagglutinin (PHA), corrected by in vivo and in vitro supplementation of zinc .
In studies measuring changes in intracellular ions such as calcium and magnesium, the tools used are partially sensitive to zinc as well. Accurate measurement of intracellular zinc requires indicators with high zinc selectivity. Currently, the single wavelength dye FluoZin-3 (Invitrogen) responds to small zinc loads, is insensitive to high calcium and magnesium ions, and is relatively unaffected by low pH or oxidants . It is noteworthy that FluoZin-3 fluorescence is non-ratiometric and thus precludes a precise quantitative determination of labile zinc, a long sought after goal. Measuring "free zinc" is complicated by the relative abundance of unoccupied high-affinity binding sites in most cells. Correctly ascertaining free zinc would depend on several factors, including the buffering capacity and the dissociation constant of the zinc chelating agent [45, 46].
Zinc and the Immune Response
Zinc deficiency affects multiple aspects of innate and adaptive immunity, the consequences of which in humans include thymic atrophy, altered thymic hormones, lymphopenia, and compromised cellular-and antibody-mediated responses that result in increased rates and duration of infection. Zinc deficiency also plays a role in the immunosenescence of the elderly . Changes in gene expression for cytokines, DNA repair enzymes, zinc transporters, and signaling molecules during zinc deficiency suggest that cells of the immune system are adapting to the stress of suboptimal zinc . Furthermore, oral zinc supplementation improves immunity and efficiently down-regulates chronic inflammatory responses . These general findings suggest that zinc is critical for normal immune cell function, whereby zinc depletion causes immune cell dysfunction, and zinc supplementation can either restore function in the setting of dysfunction or improve normal immune cell function .
Zinc and Adaptive Immunity
Zinc and Immune Cell Functions
MT-knockout results in defects in phagocytosis and antigen presentation
Zinc induces maturation and increases surface MHCII
Zinc increases cytotoxicity and restores IFN-γ production
Zinc release from MTs in limited during chronic stress. Stress and inflammation induce MT gene expression, further sequestering zinc
Cells lacking PLZF lack innate cytotoxicity and do not secrete IL-4 and IFN-γ
Zinc deficiency elevates glucocorticoid levels, causing apoptosis and reduced numbers of thymocytes
CD4 helper T cells
Zinc deficiency shifts Th1 to Th2 response via altered cytokine release
Zinc deficiency results in reduced numbers of thymocytes due glucocorticoid-induced apoptosis
Zinc deficiency results in decreased function due reduced biologically active thymulin
Required for IL-6 and TNF-α production
Zinc and Proteins of Immunological Significance
Zinc inhibits Calcineurin activity in Jurkat cells
Lung zinc exposure increases COX-2
Cytosolic caspase-3 activity is increased in Zn-deficient cells. May be mediated by the cytoprotectant abilities of zinc
Zinc deficiency increased E-selectin gene expression
FC epsilon RI
Mast cell activation downstream of FC epsilon requires zinc
3 Cys, 2 His, unknown role of zinc
Zinc increased basal/stress-induced Hsp70 in CD3+ lymphocytes
ZIP8 influences INF-gamma in T cells
Zinc suppresses IL-1 beta expression in monocytes
High zinc decreased IL-2 in T cell line, Jurkat cells
High zinc decreased IL-2R α in T Cell Line
Zinc modulated circulating cytokine in elderly patients
Zinc is necessary for the inhibitory function of KIRs
Zinc modulated circulating MCP-1 in elderly patients
MHC Class II
There is zinc dependent binding site where super-antigens and peptides bind
NFkB p65 DNA-binding activity increased by zinc deficiency (sepsis). Zinc regulates NFkB. High zinc decreases NFkB activation in T Cell Line. Zinc activates NFkB in T cell line. IKK gamma zinc finger, can regulate NFkB
Zinc reversibly inhibited enzyme activity of phosphodiesterases.
Zinc deficiency down-regulated PPAR-α
Zinc can inhibit proteasome
Zinc limits TLR surface expression
Zinc suppresses TNF-α expression in T-Cells, monocytes
Zinc finger proteins
A20 zinc finger
Modulates TLR-4 signaling, Inhibits TNF-induced apoptosis
BCL-6 Like Zinc Finger, Immune responses
Antagonizes NFkB p65, Upstream of TNF
Zinc finger that regulates NFkB
Expressed in iNKT cells. iNKT cells lacking PLZF lack innate cytotoxicity and do not secrete IL-4 or IFN-γ
Zinc Finger protein that inhibits NFkB
Zinc deficiency adversely affects lymphocyte proliferation. Zinc deficient conditions are associated with elevated glucocorticoids, which cause thymic atrophy and accelerate apoptosis in thymocytes, thereby reducing lymphopoiesis [50, 51]. In murine studies, zinc-deficient diets cause substantial reductions in the number of CD4+ and CD8+ thymocytes with the observation. Naïve cells sustain high levels of apoptosis in response to zinc-deficiency-induced elevated levels of glucocorticoids. Mature CD4+ and CD8+ T cells are resistant to zinc deficiency and can survive thymic atrophy, possibly because of higher levels of the anti-apoptotic protein BCL2 [48, 52]. Interestingly, myelopoiesis is preserved in zinc deficiency, thereby sustaining some aspects of innate immunity.
Arguably the most prominent effect of zinc deficiency is a decline in T cell function that results from multiple causes. First, thymulin, a hormone secreted by thymic epithelial cells that is essential for the differentiation and function of T cells, requires zinc as a cofactor and exists in the plasma in a zinc-bound active form, and a zinc-free, inactive form . In mice with normal thymic function, zinc deprivation reduces the level of biologically active thymulin in the circulation , thereby reducing the number of circulating T cells. Zinc supplementation reverses this effect [54, 55].
Second, zinc deficiency leads to altered gene expression in T cells resulting in an imbalance between the peripheral functions of the Th1 and Th2 cell populations . Zinc deficiency decreases production of the Th1 cell cytokines, IFN-γ, IL-2, and tumor necrosis factor (TNF)-α, which play major roles in tumor suppression. These in turn inhibit the functional capacity of these cells. Production of the Th2 cytokines IL-4, IL-6, and IL-10 are not affected. Regeneration of CD4+ T lymphocytes and CD8+ CD73+ CD11b-, precursors of cytolytic T cells, are decreased in zinc-deficient subjects with impaired immune function. An imbalance between Th1 and Th2 cells, decreased recruitment of T naive cells, and decreased percentage of T cytolytic cells are likely responsible for the cell-mediated immune dysfunction observed in zinc-deficient subjects [56, 57].
Third, in mice, modest zinc deficiencies alter levels of specific thymic mRNA and proteins even before alterations occur in thymocyte development. Specifically, zinc deficiency depresses expression of myeloid cell leukemia sequence-1 (MCL1), the longer product enhancing cell survival while the alternatively spliced (shorter) form promoting apoptosis. It also enhances expression of the DNA damage repair and recombination protein 23B (RAD23B), and the mouse laminin receptor (LAMR1) and the lymphocyte-specific protein tyrosine kinase (LCK) , perhaps as secondary effects. Conversely, zinc supplementation suppresses the development of Th17 cells in both mouse models and cultured human and mouse leukocyte cell lines. In vivo and in vitro, zinc inhibits IL-6 induced phosphorylation of STAT3, and this observation could in part explain how zinc impedes the formation of a Th17 response .
Role in Innate Immunity
Natural killer (NK) cells, dendritic cells (DCs), macrophages, mast cells, granulocytes, and complement components represent central elements of innate immunity. As observed in adaptive immune cell function, zinc deficiency results in immune dysfunction in innate immunity as well. Specifically, zinc deficiency reduces the lytic activity of natural killer cells, impairs NKT cell cytotoxicity and immune signaling, impacts the neuroendocrine-immune pathway, and alters cytokine production in mast cells [60–62]. Zinc supplementation enhances innate immunity against enterotoxigenic E.coli infection in children due to increases in C3 complement, enhanced phagocytosis, and T cell functionality .
Zinc deficiency reduces NK cell lytic activity in zinc deficient patients, while zinc supplementation improves NK cell functions. For example, zinc treatment at physiological doses for one month in elderly infected patients, increases NK cell cytotoxicity and enhances recovery of IFN-γ production leading to a 50% reduction in relapse of infection . Additionally, in vitro, zinc supplementation improves the development of NK cells from CD34+ cell progenitors via increased expression of GATA-3 transcription factor . Notably, centenarians have well-preserved NK cell cytotoxicity, zinc ion bioavailability, satisfactory IFNγ production, and preserved thyroid hormone turnover , suggesting the importance of zinc in maintaining both NK cell function and the immunologically involved neuroendocrine pathway in the elderly. Its role in regulating Class I MHC molecules has not been extensively studied, but it does appear that it is critical for HLA-C interaction with killer cell Ig-like receptors (KIRs). Interestingly, the kinetics of the binding of KIR to their respective individual Class I MHC ligands is altered significantly in the presence of zinc, but not other divalent cations. Zinc-induced multimerization of the KIR molecules may be critical for formation of KIR and HLA-C molecules at the interface between the NK cell and target cells .
Metallothioneins (MTs), small cysteine-rich proteins that bind zinc as well as other metal ions, mediate zinc homeostasis, and are therefore critical to not only NK function but also other cellular functions. Recent studies in aging show a novel polymorphism in the MT1A coding region in MT genes that affects NO-induced zinc ion release from the protein . Other polymorphisms in MT genes impair innate immunity, further confirming a link among zinc, MT, and the innate immune response during aging.
NKT cells are a bridge between the innate and the adaptive immune systems , displaying both cytotoxic abilities as well as providing signals required for driving the adaptive immune response. Both zinc and MTs affect NKT cell development, maturation, and function. In conditions of chronic stress including aging, zinc release by MTs is limited, leading to low intracellular zinc bioavailability and subsequent reduced immunity . Furthermore, during stress and inflammation, expression of MTs is induced by the pro-inflammatory cytokines IL-1, IL-6, and tumor necrosis factor (TNF)-α , resulting in further sequestration of zinc by MTs .
Additionally, some zinc finger motifs play an important role in the immune response of NKT cells. The BTB-ZF transcriptional regulator, promyelocytic leukemia zinc finger (PLZF), is specifically expressed in invariant natural killer T (iNKT) cells (Table 2). In the absence of PLZF, iNKT cells have markedly diminished innate cytotoxicity and do not secrete IL-4 or IFN-γ following activation . Thus, zinc deficiency causes a reduction in both innate and adaptive immune functioning in NKT cells.
Hormones from the hypothalamic-pituitary-gonadal axis (i.e. FSH, ACTH, TSH, GH, T3, T4, insulin, and the sex hormones) directly affect the innate immune response, interacting with hormone receptors on immune cells, including NK cells. Hormonally activated NK cells produce cytokines that mediate adaptive immune responses. Deficient production of these hormones impairs innate and adaptive immune response in aging. The beneficial effects of hormone supplementation on immunity are mediated in part by enhanced intestinal zinc absorption. Therefore, zinc is a nutritional factor pivotal in maintaining the neuroendocrine-immune axis .
Dendritic cells (DCs)
In mast cells, an increase in intracellular free zinc, known as the 'zinc wave', occurs within minutes of extracellular stimulation . This rapid response in mast cells is in contrast to changes observed in intracellular zinc in DCs, which are dependent on transcriptional regulation in zinc transporters and are therefore observed several hours following stimulation. Zinc deficiency in mast cells prevents translocation of PKC and downstream events such as the phosphorylation and nuclear translocation of NFκB as well as the downstream production of the cytokines IL-6 and TNFα . Additionally, the granules of mast cells (and other immune cells) have high concentrations of zinc, which upon release could alter the extracellular milieu as well as immune, stromal, and epithelial/tumor cell functions.
Macrophages from metallothionein knockout (MT-KO) mice have defects in phagocytosis, cytokine production, and antigen presentation . Production of IL-1., IL-6, IL-10, and IL-12 as well as the expression of CD80, CD86 and MHC Class II molecules are reduced in macrophages from MT-KO mice. Therefore, zinc regulation by MTs plays an important role in the regulation of macrophage immune function. In some studies, zinc supplementation of human PBMCs increases mRNA production and subsequent release of the cytokines IL-6, IL-1β, and TNF-α , promoting the recruitment of leukocytes to the site of infection . Conversely, zinc treatment suppresses the formation of pro-inflammatory cytokines [75, 76]. It is thought that the effect of zinc is concentration dependent, and that zinc can be either stimulatory or inhibitory: an increase of intracellular free zinc induces cytokine production of monocytes in response to LPS , while higher concentrations can have the opposite effect by inhibiting cyclic nucleotide phosphodiesterases and subsequently activating protein kinase A [34, 39]. Zinc can also suppress monocyte LPS-induced tumor necrosis factor (TNF)-α and IL-1β release, through inhibition of phosphodiesteras-mediated hydrolysis of cyclic nucleotides into 5′-nucleotide monophosphate and increases of intracellular cGMP levels. The NO donor s-nitroso-cysteine (SNOC) also inhibits LPS-induced TNF-α and IL-1β release, and increased levels of intracellular free zinc .
Zinc has also been shown to be important regulators of immunity through its impact on non-circulating cells. Zinc deficiency promotes sepsis invoked organ damaged due to its effects in the epithelial cells of most organs . In the lung parenchyma for example, zinc can act to diminish inflammation, and promote cell health and survival .
Role in Oncogenesis
Zinc helps to maintain intracellular ion homeostasis and contributes to signal transduction in most cells. As such, zinc directly affects tumor cells through its regulatory role in gene expression and cell survival, both of which are controlled at least in part by tumor-induced alterations in zinc transporter expression, and influences tumor cells indirectly by affecting the activation, function, and/or survival of immune cells .
Zinc Levels in Tumor Tissue
Breast, gallbladder, colon, bronchus, lung
Decreased serum zinc
Liver, kidney, lung
Increased zinc in peritumor tissue as compared to both normal tissue and tumor itself
Breast, lung (likely others except prostate)
Increased zinc in tumor tissue
Decreased zinc in tumor tissue
Head and Neck
Increasing zinc improves local free survival, Decreased serum zinc near end of life
Zinc Transporters (Importers) and Cancer
In the vesicular compartment and partly in the ER in adherent cells
Squamous cell carcinoma
mRNA is induced by contact inhibition and serum starvation
ZIP1, ZIP2, ZIP3
Down-regulated in malignant cells
Over-expression is linked to increased cell proliferation
Expression is linked to metastasis to lymph node
Tamoxifen resistant breast cancer
Increased levels results in increased growth and invasion
Prostate tumor cells and skin cancer are the exception to these findings, in that zinc levels are lower in prostate tumor tissue than in normal prostate cancer [86, 88]. Prostate glandular epithelium has the specialized function of producing and secreting large quantities of citrate, and thus requires metabolic activities that are unique to these cells. Zinc accumulation in these cells is critical to their specialized metabolism. In malignant prostate cells, the normal zinc-accumulating epithelial cells undergo a metabolic transformation causing them to lose the ability to accumulate zinc. Genetic alteration in the expression of the ZIP1 zinc importer is associated with a metabolic transformation analogous to the changes observed in malignant prostate. In fact, ZIP1, ZIP2, and ZIP3 are down-regulated in prostate cancer cells, suggesting that changes in intracellular zinc play a role in tumorigenesis. In a study by Gonzalez et al. , dietary zinc was not associated overall risk of prostate cancer, but long-term supplemental zinc intake was associated with reduced risk of advanced prostate cancer. Authors note much variability in current studies correlating zinc and prostate cancer. High extracellular zinc is also important, since it was shown to induce cytotoxicity in human pancreatic adenocarcinoma cell lines. Normal human pancreatic islet cells tolerated high zinc, making zinc elevation a potential treatment avenue . Zinc could prevent UVB-induced aging and skin cancer development through the induction of HIF-1alpha, a protein that controls the keratinocyte cell cycle, and is down-regulated by UVB and therefore involved in UVB-induced skin hyperplasia .
HDAC inhibitors are being used as anticancer agents given their wide range of substrates, including proteins that have roles in gene expression, cell proliferation, cell migration, cell death, immune pathways, and angiogenesis. There are eleven zinc dependent HDACs in humans. The synergy of HDAC is with current anti-cancer therapies including radiation, anti-metabolites, anti-microtubule agents, topoisomerase inhibitors, DNA cross-linking agents, monoclonal antibodies, and EFGR inhibitors have been the topic of many studies . Other zinc-finger transcription factors may directly influence tumor formation through the epithelial-mesenchymal transition. SNAIL, MUC1, ZEB1 are known to influence the transition away from non-tumorous epithelial lineages back to the more invasive lineages, and are effected by zinc changes [93–95].
Zinc levels are directly affected by the tumor microenvironment. Pro-inflammatory mast cells are found within the cancer microenvironment and release granules with high levels of zinc into the surrounding tissue . Mast cell presence within tumors is thought to worsen the prognosis of most patients with cancer, and changes in extracellular zinc affect the cellular response in the tumor environment. Many cytokines and growth factors produced in the tumor microenvironment, including IL-6, hepatocyte growth factor, epidermal growth factor, and TNF-α, directly or indirectly affect the expression of various zinc transporters , thereby changing the intracellular concentrations of zinc in both tumor cells and neighboring tissues (see following section). Furthermore, it is likely that the activities of many enzymes and transcription factors that require zinc to function are affected by the altered zinc concentrations found within the cancer microenvironment. Oxidation/reduction reactions in tumors and surrounding tissues influence intracellular free zinc concentrations  and indeed, zinc levels may be an early intracellular 'reporter' of reactive oxygen species and subsequent biologic responses.
Zinc Transport and Cancer
Apoptosis is an active, gene-directed, tightly-regulated process of programmed cell death that involves a series of cytoskeletal, membrane, nuclear, and cytoplasmic changes that culminate in condensation and fragmentation of the cell into apoptotic bodies, which are eventually cleared by phagocytosis . Apoptosis is the major mechanism of cell death in the body, enabling the removal of excess, mutant, or damaged cells. In contrast to necrosis, apoptosis deletes cells without release of their contents that would otherwise provoke and possibly damage neighboring cells and result in an inflammatory response. Apoptosis consumes energy, and involves signaling pathways originating from the plasma membrane (TNF receptor family molecules including the Fas receptor ligation or lipid peroxidation), the nucleus (DNA damage/mutation) or the cytoskeleton (disruption of microtubules) .
The mitochondrion has a major role in the induction, regulation, and execution of apoptosis. Mitochondria coordinate apoptosis by channeling various input signals into a central pathway, which is governed by mitochondrial-associated anti-apoptotic (Bcl-2) and pro-apoptotic (Bax) families of regulators and by providing an environment for the proteolytic events that trigger processing and activation of various members of the caspase enzyme family . Action of the caspases leads to morphological changes such as cell shrinkage, condensation and fragmentation of both the cytoplasm and nucleus and formation of membrane-enclosed apoptotic bodies [111, 112].
Apoptosis is tightly regulated and its deregulation is central to the pathogenesis of a number of diseases--increased in neurodegenerative disorders, AIDS, and diabetes mellitus, and decreased in autoimmune disease and neoplastic malignancies [113, 114]. As such, the factors that regulate the execution phases of apoptosis are of great interest as potential therapies. One of these regulators is zinc.
Zinc and Apoptosis
At the beginning of this decade Truong-Tran et al. assembled a core picture of zinc's role in apoptosis . In this picture, the presence of zinc is anti-apoptotic, and this apoptotic effect has two aspects. Firstly, zinc may directly protect cells against oxidative damage. An example of this mechanism would be the thiolate complexes that zinc forms with sulfhydryl groups in proteins. This complex is strong enough to protect and prevent protein oxidation by ROS, but is still reversible. Secondly, evidence suggested that zinc might inhibit caspase-3 activation, perhaps, again, through forming a complex with a sulfhydryl group, in this case preventing proteolysis. There have also been some studies which imply the contrary, due to zinc's ability to inhibit important ROS-protective enzymes [115, 116]. In mouse DCs, zinc induces apoptosis by stimulating the formation of ceramide . Similar events are observed in erythrocytes, where zinc induces secretory sphingomylenase, which produces ceramide leading to apoptosis .
Although high concentrations of zinc may trigger cell death by apoptosis or necrosis [119–122]in many settings, zinc is a physiological suppressor of apoptosis. There are two major anti-apoptotic mechanisms of zinc: it directly influences apoptotic regulators, especially the caspase family of enzymes, and it may prevent oxidative damage and damage induced by toxins, thereby suppressing the caspase activating pathways and apoptosis. These two mechanisms are closely related since a decline in intracellular zinc below a critical level may not only trigger pathways leading to caspase activation via increased oxidative stress, but may also directly facilitate the process by which the caspases are activated .
Zinc deficiency-induced apoptosis in vitro and in vivo displays all of the fundamental characteristics of apoptosis, including DNA and nuclear fragmentation, chromatin condensation and apoptotic body formation , indicating that apoptosis is directly related to the decrease in intracellular zinc. Zinc deficiency decreases cell proliferation and increases apoptosis in neuroblastoma IMR-32 cells. In these cells, low zinc arrests the cell cycle at G0/G1 phase, and induces apoptosis through the intrinsic pathway . Specifically, cytosolic caspase-3 activity is increased in zinc deficient cells, and zinc suppresses caspase-3 activity and apoptosis in rats in vivo . Taken together, this demonstrates that zinc deficiency-induced apoptosis is dependent on caspase-3 activation. Interestingly, in zinc deficiency, the frequency of apoptotic cells is significantly increased in specific tissues, including the intestinal and retinal pigmented epithelium, skin, thymic lymphocytes, testis and pancreatic acinar cells [126, 127] and neuroepithelium . The importance of these observed localizations has yet to be elucidated.
In 2010, our understanding of the role of zinc has progressed to the point where we understand zinc's role in apoptosis to involve both direct effects on mitochondria and the nucleus as well as on various factors and signaling pathways within and between the cytosol, mitochondria, and nucleus. We also know that within some cell types including neurons, glial cells, and prostate epithelial cells, zinc may be pro-apoptotic . Still, many of the precise mechanisms through which zinc regulates apoptosis and proliferation remain to be elucidated. Interestingly a pro-apoptotic compound which increases the conversion of pro-caspase 3 to the active caspase 3 form was found to operate through the sequestration of the zinc that inhibits cleavage of the pro-caspase 3 .
Many animal studies have linked zinc deficiency with enhanced rates of oxidative damage [131–133]. Zinc supplementation also protects against intracellular oxidative damage. Zinc depletion increases the rate of apoptosis, and there is a synergy in the induction of apoptosis between zinc depletion and other apoptotic inducers such as colchicine, tumor necrosis factor and HIV-1 Tat protein [134, 135]. Therefore, major reductions in intracellular zinc can directly induce apoptosis, while smaller decreases may increase cell susceptibility to apoptosis by other toxins.
Zinc is a cytoprotectant, and as such it protects and stabilizes proteins, DNA, cytoskeleton, organelles, and membranes , reminiscent of survival factors associated with autophagy. For instance, axons and dendrites exposed to zinc chelators (TPEN and zinquin) slowly "die back", due to metabolic lack of neuronal ATP, which can be resolved with addition of NAD . Zinc can also up-regulate MT, which stabilize lysosomes and decrease apoptosis resulting from oxidative stress, due to increases in autophagy . Cytoprotective zinc is most likely the exchangeable (loosely bound or tightly bound but kinetically labile) zinc pools [97, 134, 136]. Zinc protects sulfhydryl groups in proteins from oxidation by forming strong, reversible, thiolate complexes, and as such provides protection to enzymes with essential thiols such as tubulin, where sulfhydryls are required for polymerization into microtubules [139, 140]. As such, zinc is a stabilizer of microtubules, and microtubule disruption occurs in zinc deficiency , oxidative stress  and in the early stages of apoptosis . It is also important to note that TPEN itself or TPEN-Zinc complexes may actually be the cause of increased apoptosis in some of these experiments .
Supplementing cells with exogenous zinc in vitro decreases the susceptibility of cells and tissues to spontaneous or toxin-induced apoptosis. In several studies, zinc-supplemented animals have increased resistance to apoptotic inducers. For example, zinc has protective effects against whole body irradiation in mice , neuronal apoptosis following transient forebrain ischemia in the hippocampus of primates , and apoptosis of the anterior and stromal keratinocytes in the eye following superficial keratectomy in rabbits . PBLs pretreated with zinc are resistant to Cr(III)(phe)3 induced apoptosis. This reduced apoptosis correlated with decreased ROS production in cells pretreated with zinc . Zinc blocks apoptosis induced by all apoptosis-inducing treatments tested, indicating that it suppresses a central pathway [127, 135, 149]. Monocytes in chronic HIV viremia are resistant to apoptosis. Expression of MTs, which are highly involved in cellular zinc metabolism, and ZIP8 zinc importer are up-regulated in these monocytes. Increased intracellular zinc, therefore, may play a role in the apoptotic resistance seen in monocytes during HIV viremia .
There are several issues, however, with zinc supplementation studies and their interpretation. There is relatively poor uptake of ionic zinc across the plasma cell membrane, and mM concentrations of zinc can cross-link proteins nonspecifically, rendering interpretation difficult. Exogenous zinc driven into cells with an ionophore, such as pyrithione, has resolved many of the zinc uptake issues, but presents a secondary problem. Many zinc ionophores act on other cellular cations such as calcium and magnesium . Additionally, using ionophores may produce much higher intracellular zinc levels than would occur in vivo. Metabolically available zinc is distributed non-uniformly throughout the cell with nM-pM concentrations in the cytosol and up to mM concentrations within vesicles . It is unknown whether zinc supplementation affects the same pools and apoptotic targets as does zinc depletion.
Zinc, Apoptosis and Cancer
Role in Necrosis
In some cells, zinc deprivation results in necrosis. The reason for this has not yet been elucidated, but may depend on the functional state of activated caspases. In TPEN-induced zinc-deficient human renal cell carcinoma cell lines lacking caspases-3, -7, -8 and -10 died by necrosis rather than apoptosis . In these cases, zinc may not regulate apoptosis, but rather function as a cytoprotectant that, in zinc-deficient conditions, leaves the cell vulnerable to apoptosis and necrosis.
Zinc and Autophagy
Normal cellular growth and development require a balance between protein synthesis and degradation. Eukaryotic cells have two major avenues for degradation: the proteasome and autophagy . Autophagy, literally 'self-eating', is involved in the bulk degradation of long-lived cytosolic proteins and organelles, whereas the ubiquitin-proteasome system degrades specific short-lived proteins. Autophagy is a highly conserved process in eukaryotes in which excess or aberrant organelles and their surrounding cytoplasm are sequestered into double-membrane vesicles and delivered to the lysosome for breakdown and eventual recycling of the resulting macromolecules. There are three types of autophagy, the first of which, chaperone-mediated autophagy, is a mechanism that allows the degradation of cytosolic proteins that contain a particular pentapeptide consensus motif [154, 155]. The two other types of autophagy, macro-autophagy and microautophagy, involve dynamic membrane rearrangements and terminate at the lysosome [156, 157] with fusion and degradation. Microautophagy is a direct engulfment of cytoplasm at the surface of the degradative organelle by protrusion, septation, and/or invagination of the membrane, while macroautophagy involves sequestering cytoplasm into a double-membrane cytosolic vesicle, the autophagosome . Autophagosomes fuse with the lysosome, the contents are degraded, and the macromolecules recycled.
Autophagy has an important role in various biological events such as adaptation to changing environmental conditions [158, 159], cellular remodeling during development and differentiation, and determination of lifespan . Autophagy may play a protective role against the progression of some human diseases, including cancer, muscular disorders, and neurodegeneration, such as Huntington's, Alzheimer's, and Parkinson's diseases [160–162], and acts as a cellular defense mechanism to prevent infection by certain pathogenic bacteria and viruses [162–164]. Autophagy is involved in some forms of cell death and might contribute to the pathology of associated diseases [157, 165].
Endogenous zinc levels appear to be critical to induce autophagy under conditions of oxidative stress in astrocytes. Autophagy is a necessary preceding event for lysosomal membrane permeabilization and cell death in oxidative injury . When autophagy is induced in astrocytes, the number of autophagic vacuoles positive for LC3 (microtubule-associated protein 1 light chain 3), a marker of autophagy, increases, and levels of labile zinc increase in autophagic vacuoles as well as in the cytosol and nuclei. Interestingly, chelation of zinc with TPEN decreases the number of autophagic vacuoles in autophagy-induced astrocytes, similar to the effects observed with autophagy inhibitors (3-methyladenine, bafilomycin-1). Conversely, exposure to zinc increases the number of autophagic vacuoles. Taken together, these findings suggest that zinc is critical to autophagy. Possibly related to zinc's role in autophagy, ethambutol, an anti-tuberculosis agent, can cause irreversible vision loss, associated with severe vacuole formation in cultured retinal cells. In ethambutol-treated cultured retinal cells, almost all ethambutol-induced vacuoles contained high levels of labile zinc. Intracellular zinc chelation with TPEN blocks both vacuole formation and zinc accumulation in the vacuole, and inhibits lysosomal activation and lysosomal membrane permeabilization . Although there are examples of zinc's effect on autophagy in bacteria and yeast , it is not as clear how these can be translated to mammals. Zn mediates tamoxifen-induced autophagy in breast cancer cells , hippocampal neurons , retinal cells , and in astrocytes via increases in oxidative stress and induction of lysosomal membrane permeabilization . The newer studies have used animals deficient in metallothionein to study the changes and importance of zinc. Again, autophagy is now seen as a mechanism that tumor cells use to promote their survival, even in face of potent chemotherapies .
The alterations of free zinc concentration and zinc transporters in maturing dendritic cells suggest another, as yet unexplored intersection between zinc regulation and autophagy. After all, the activation of autophagy mechanisms is a second defining feature of DC maturation and effective MHC-II antigen loading .
Significant disorders of great public health interest are associated with zinc deficiency. The amelioration of a number of common conditions with zinc supplementation in the context of malnutrition has underscored the importance of this micronutrient. Rapid advances in molecular biology and genetics have revealed the complexities in zinc homeostasis and the attendant pathophysiology of mutations in critical genes affecting usually well controlled intra-and extracellular levels of zinc. It is apparent that a labile pool of zinc contributes to a myriad of cell signaling processes providing critical insight into the role of zinc in health and disease. In the immune system, we now know that this pool can affect function, differentiation, maturation and cell death pathways in critical immunocytes thereby contributing to many aspects of innate and adaptive immunity. Similar observations are apparent in tumor cells and the critical contribution of immune cells in the microenvironment and pathogenesis of cancer underscores the potential connection between zinc homeostasis and oncology. Manipulating zinc levels in adoptively transferred immune cells thus may be an interesting and important means to alter their function, and promote either tolerance or immunity. Though biologically significant, exogenous zinc may be too blunt a tool for targeting some zinc dependent cellular processes. Drugs and treatments capable of targeting zinc levels of specific pools within the cell or that inhibit zinc binding to a restricted class of protein, may be more effective in this regard.
Among the critical limitations in advancing our understanding of the role of zinc in tumor immunology are: a) availability of quantitative zinc sensors (e.g. ratiometric fluorophores, genetically encoded and easily used detectors, etc) for cellular and organ physiology; b) improved analytical tools to approach the zinc proteome in earnest and in a more high throughput conducive fashion; c) needed progress in biomarkers of zinc deficiency and/or imaging of zinc in medicine in addition to current rather difficult to interpret measurements of total zinc in various biological compartments; d) more complete information on polymorphisms in various zinc transporters, importers and binding proteins; and e) methods of targeting specific subcellular pools of zinc. It is quite likely that alterations in zinc homeostasis may be a contributing factor in genetic alternations (ZNT, ZIP, metallothionein, etc) or environmental causes (nutritional status, exposure to zinc, microbial control) playing a role in the genesis and/or maintenance of cancer. Its role in HMGB1 and RAGE signaling in cancer has not been fully explored [173–175]. As such, a rational approach towards zinc supplementation and modulation may ultimately emerge in the context of preventing or treating immunologic and oncologic disorders.
The author's research is supported by NIH P01 CA 101944-04 and the University of Pittsburgh Cancer Institute. We would like to acknowledge our Cancer Center director, Nancy Davidson, MD.
- Rink L, Gabriel P: Zinc and the immune system. Proc Nutr Soc. 2000, 541-10.1017/S0029665100000781.Google Scholar
- Wapnir AR: Protein Nutrition and Mineral Absorption. 1990, CRC Press, Boca RatonGoogle Scholar
- Berdanier DC, Dwyer JT, Feldman EB: Handbook of Nutrition and Food. 2007, CRC Pres, Boca RatonGoogle Scholar
- Raulin J: Chemical studies on vegetation. Annales des Sci Naturelles. 1869, 11: 93-99.Google Scholar
- Sommer AL, Lipman CB: Evidence on indispensable nature of zinc and boron for higher green plants. Plant Physiol. 1926, 1: 231-10.1104/pp.1.3.231.PubMedPubMed CentralGoogle Scholar
- Todd WR, Elvehjem CA, Hart EB: Zinc in the nutrition of the rat. Am J Physiol. 1933, 107: 146-156.Google Scholar
- Follis RH, Day HG, McCollum EV: Histological studies of the tissues of rats fed a diet extremely low in zinc. J Nutr. 1941, 22: 223Google Scholar
- Tucker HF, Salmon WD: Parakeratosis or zinc deficiency disease in the pig. Proc Soc Exp Biol. 1955, 88: 613PubMedGoogle Scholar
- Blencowe DK, Morby AP: Zn(II) metabolism in prokaryotes. FEMS Microbiol Rev. 2003, 27: 291-311. 10.1016/S0168-6445(03)00041-X.PubMedGoogle Scholar
- Prasad AS: Zinc: an overview. Nutrition. 1995, 11: 93-99.PubMedGoogle Scholar
- Prasad AS: Zinc in human health: an update. J Trace Elements Exp Med. 1998, 11: 63-87. 10.1002/(SICI)1520-670X(1998)11:2/3<63::AID-JTRA2>3.0.CO;2-5.Google Scholar
- Joazeiro CA, Weissman AM: RING finger proteins: mediators of ubiquitin ligase activity. Cell. 2000, 102: 549-552. 10.1016/S0092-8674(00)00077-5.PubMedGoogle Scholar
- Kadrmas JL, Beckerle MC: The LIM domains: from the cytoskeleton to the nucleus. Nat Rev Mol Cell Biol. 2004, 5: 920-931. 10.1038/nrm1499.PubMedGoogle Scholar
- Vallee BL: The function of metallothionein. Neurochem Int. 1995, 27: 23-33. 10.1016/0197-0186(94)00165-Q.PubMedGoogle Scholar
- National Institutes of Health, Office of Dietary Supplements: Zinc: Health Professional Fact Sheet. [http://ods.od.nih.gov/FactSheets/Zinc.asp]
- Institute of Medicine, Food and Nutrition Board: Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. 2001, Washington, DC: National Academy PressGoogle Scholar
- Gropper SS, Smith JL, Groff JL: Advanced nutrition and human metabolism. 2009, Belmont, CA: WadsworthGoogle Scholar
- Brown H, Peerson JM, Allen LH, Rivera J: Effect of supplemental zinc on the growth and serum zinc concentrations of pre-pubertal children: a metaanalysis of randomized, controlled trials. Am J Clin Nutrition. 2002, 75: 1062-1071.Google Scholar
- Prasad AS, Halsted JA, Nadimi M: Syndrome of iron deficiency anemia, hepatosplenomegaly, hypogonadism, dwarfism and geophagia. Am J Med. 1961, 31: 532-546. 10.1016/0002-9343(61)90137-1.PubMedGoogle Scholar
- Bhutta ZA, Bird SM, Black RE: Therapeutic effects of oral zinc in acute and persistent diarrhea in children in developing countries: pooled analysis of randomized controlled trials. Am J Clin Nutr. 2000, 72: 1516-1522.PubMedGoogle Scholar
- Dutta SK, Procaccino F, Aamodt R: Zinc metabolism in patients withexocrine pancreatic insufficiency. J Am Coll Nutr. 1998, 17: 556-563.PubMedGoogle Scholar
- Fraker PJ, King LE, Laakko T, Vollmer TL: The dynamic link between the integrity of the immune system and zinc status. J Nutr. 2000, 130: 1399-1406.Google Scholar
- Prasad AS: Clinical and biochemical manifestation zinc deficiency in human subjects. J Pharmacol. 1985, 16: 344-352.PubMedGoogle Scholar
- Tapazoglou E, Prasad AS, Hill G, Brewer GJ, Kaplan J: Decreased natural killer cell activity in patients with zinc deficiency with sickle cell disease. J Laboratory Clin Med. 1985, 105: 19-22.Google Scholar
- Zemel BS, Kawchak DA, Fung EB, Ohene-Frempong K, Stallings VA: Effect of zinc supplementation on growth and body composition in childrenwith sickle cell disease. Am J Clin Nutr. 2002, 75: 300-307.PubMedGoogle Scholar
- Chue CD, Rajpar SF, Bhat J: An acrodermatitis enteropathica-like eruption secondary to acquired zinc deficiency in an exclusively breast-fed premature infant. Int J Dermatol. 2008, 47 (4): 372-3. 10.1111/j.1365-4632.2008.03492.x.PubMedGoogle Scholar
- Mocchegiani E, Costarelli L, Giacconi R, Cipriano C, Muti E, Malavolta M: Zinc-binding proteins (metallothionein and alpha-2 macroglobulin) and immunosenescence. Exp Gerontol. 2006, 41: 1094-1107. 10.1016/j.exger.2006.08.010.PubMedGoogle Scholar
- Roth DE, Richard SA, Black RE: Zinc supplementation for the prevention of acute lower respiratory infection in children in developing countries: meta-analysis and meta-regression of randomized trials. Int J Epidemiol. 2010, 39 (3): 795-808. 10.1093/ije/dyp391.PubMedGoogle Scholar
- Maret W, Sandstead HH: Zinc requirements and the risks and benefits of zinc supplementation. J Trace Elem Med Biol. 2006, 20 (1): 3-18. 10.1016/j.jtemb.2006.01.006.PubMedGoogle Scholar
- Vales-Gomez M, Erskine RA, Deacon MP, Strominger JL, Reyburn HT: The role of zinc in the binding of killer cell Ig-like receptors to class I MHC proteins. Immunology. 2000, 96: 1734-1739.Google Scholar
- Walker CL, Black RE: Zinc for the treatment of diarrhoea: effect on diarrhoea morbidity, mortality and incidence of future episodes. Int J Epidemiol. 2010, 39 (Suppl 1): 63-9. 10.1093/ije/dyq023.Google Scholar
- Li Y, Hough CJ, Suh SW, Sarvey JM, Frederickson CJ: Rapid translocation of Zn (2+) from presynaptic terminals into postsynaptic hippocampal neurons after physiological stimulation. J Neurophysiol. 2001, 86: 2597-2604.PubMedGoogle Scholar
- Csermely P, Somogyi J: Zinc as a possible mediator of signal transduction in T lymphocytes. Acta Physiol Hung. 1989, 74: 195-199.PubMedGoogle Scholar
- Haase H, Rink L: The immune system and the impact of zinc during aging. Immun Ageing. 2009, 6: 9-10.1186/1742-4933-6-9.PubMedPubMed CentralGoogle Scholar
- Romir J, Lilie H, Egerer-Sieber C, Bauer F, Sticht H, Muller YA: Crystal structure analysis and solution studies of human Lck-SH3; zinc-induced homodimerization competes with the binding of proline-rich motifs. J Mol Biol. 2007, 365: 1417-1428. 10.1016/j.jmb.2006.10.058.PubMedGoogle Scholar
- Lefebvre DC, Lai JC, Maeshima N, Ford JL, Wong AS, Cross JL, Johnson P: CD44 interacts directly with Lck in a zinc-dependent manner. Mol Immunol. 2010, 47 (10): 1882-9. 10.1016/j.molimm.2010.03.018.PubMedGoogle Scholar
- Kaltenberg J, Plum LM, Ober-Blöbaum JL, Hönscheid A, Rink L, Haase H: Zinc signals promote IL-2-dependent proliferation of T cells. Eur J Immunol. 2010, 40 (5): 1496-503. 10.1002/eji.200939574.PubMedGoogle Scholar
- Haase H, Ober-Blobaum JL, Engelhardt G, Hebel S, Heit A, Heine H, Rink L: Zinc signals are essential for lipopolysaccharide-induced signal transduction in monocytes. J Immunol. 2008, 181: 6491-6502.PubMedGoogle Scholar
- von Bulow V, Rink L, Haase H: Zinc-mediated inhibition of cyclic nucleotide phosphodiesterase activity and expression suppresses TNF-alpha and IL-1 beta production in monocytes by elevation of guanosine 3',5'-cyclic monophosphate. J Immunol. 2005, 175: 4697-4705.PubMedGoogle Scholar
- von Bulow V, Dubben S, Engelhardt G, Hebel S, Plumakers B, Heine H, Rink L, Haase H: Zinc-dependent suppression of TNF-alpha production is mediated by protein kinase A-induced inhibition of Raf-1, I kappa B kinase beta, and NF-kappa B. J Immunol. 2007, 179: 4180-4186.PubMedGoogle Scholar
- Gilmore TD: Introduction to NF-kB: players, pathways, perspectives. Oncogene. 2006, 25: 6680-6684. 10.1038/sj.onc.1209954.PubMedGoogle Scholar
- Bao S, Liu MJ, Lee B, Besecker B, Lai JP, Guttridge DC, Knoell DL: Zinc modulates the innate immune response in vivo to polymicrobial sepsis through regulation of NF-kappaB. Am J Physiol Lung Cell Mol Physiol. 2010, 298 (6): L744-54. 10.1152/ajplung.00368.2009.PubMedPubMed CentralGoogle Scholar
- Prasad AS, Bao B, Beck FW, Sarkar FH: Correction of interleukin-2 gene expression by in vitro zinc addition to mononuclear cells from zinc-deficient human subjects: a specific test for zinc deficiency in humans. Transl Res. 2006, 148: 325-333. 10.1016/j.trsl.2006.07.008.PubMedGoogle Scholar
- Devinney MJ, Reynolds IJ, Dineley KE: Simultaneous detection of intracellular free calcium and zinc using fura-2FF and FluoZin-3. Cell Calcium. 2005, 37: 225-232. 10.1016/j.ceca.2004.10.003.PubMedGoogle Scholar
- Bozym R, Hurst TK, Westerberg N, Stoddard A, Fierke CA, Frederickson CJ, Thompson RB: Determination of zinc using carbonic anhydrase-based fluorescence biosensors. Methods Enzymol. 2008, 450: 287-309. full_text.PubMedGoogle Scholar
- Krezel A, Maret W: Zinc-buffering capacity of a eukaryotic cell at physiological pZn. J Biol Inorg Chem. 2006, 11 (8): 1049-62. 10.1007/s00775-006-0150-5.PubMedGoogle Scholar
- Haase H, Rink L: The immune system and the impact of zinc during aging. Immun Ageing. 2009, 12: 6-9.Google Scholar
- Fraker PJ, King LE: Reprogramming of the immune system during zinc deficiency. Annu Rev Nutr. 2004, 24: 277-298. 10.1146/annurev.nutr.24.012003.132454.PubMedGoogle Scholar
- Prasad AS: Zinc: role in immunity, oxidative stress and chronic inflammation. Curr Opin Clin Nutr Metab Care. 2009, 12 (6): 646-52. 10.1097/MCO.0b013e3283312956.PubMedGoogle Scholar
- DePasquale-Jardieu P, Fraker PJ: The role of corticosterone in the loss in immune function in the zinc-deficient A/J mouse. J Nutr. 1979, 109: 1847-1855.PubMedGoogle Scholar
- DePasquale-Jardieu P, Fraker PJ: Further characterization of the role of corticosterone in the loss of humoral immunity in zinc-deficient A/J mice as determined by adrenalectomy. J Immunol. 1980, 124: 2650-2655.PubMedGoogle Scholar
- King LE, Osati-Ashtiani F, Fraker PJ: Apoptosis plays a distinct role in the loss of precursor lymphocytes during zinc deficiency in mice. J Nutr. 2002, 132: 974-979.PubMedGoogle Scholar
- Iwata T, Incefy GS, Tanaka T, Fernandes G, Menendez-Botet CJ, Pih K, Good RA: Circulating thymic hormone levels in zinc deficiency. Cell Immunol. 1979, 47: 100-105. 10.1016/0008-8749(79)90318-6.PubMedGoogle Scholar
- Dardenne M, Savino W, Wade S, Kaiserlian D, Lemonnier D, Bach JF: In vivo and in vitro studies of thymulin in marginally zinc-deficient mice. Eur J Immunol. 1984, 14: 454-458. 10.1002/eji.1830140513.PubMedGoogle Scholar
- Prasad AS, Meftah S, Abdallah J, Kaplan J, Brewer GJ, Bach JF, Dardenne M: Serum thymulin in human zinc deficiency. J Clin Invest. 1988, 82: 1202-1210. 10.1172/JCI113717.PubMedPubMed CentralGoogle Scholar
- Beck FW, Prasad AS, Kaplan J, Fitzgerald JT, Brewer GJ: Changes in cytokine production and T cell subpopulations in experimentally induced zinc-deficient humans. Am J Physiol. 1997, 272: 1272Google Scholar
- Prasad AS, Beck FW, Grabowski SM, Kaplan J, Mathog RH: Zinc deficiency: changes in cytokine production and T-cell subpopulations in patients with head and neck cancer and in noncancer subjects. Proc Assoc Am Physicians. 1997, 109: 68-77.PubMedGoogle Scholar
- Moore JB, Blanchard RK, McCormack WT, Cousins RJ: cDNA array analysis identifies thymic LCK as upregulated in moderate murine zinc deficiency before T-lymphocyte population changes. J Nutr. 2001, 131: 3189-3196.PubMedGoogle Scholar
- Kitabayashi C, Fukada T, Kanamoto M, Ohashi W, Hojyo S, Atsumi T, Ueda N, Azuma I, Hirota H, Murakami M, Hirano T: Zinc suppresses Th17 development via inhibition of STAT3 activation. Int Immunol. 2010, 22 (5): 375-86. 10.1093/intimm/dxq017.PubMedGoogle Scholar
- Muzzioli M, Stecconi R, Moresi R, Provinciali M: Zinc improves the development of human CD34+ cell progenitors towards NK cells and increases the expression of GATA-3 transcription factor in young and old ages. Biogerontology. 2009, 10 (5): 593-604. 10.1007/s10522-008-9201-3.PubMedGoogle Scholar
- Mocchegiani E, Muzzioli M, Giacconi R, Cipriano C, Gasparini N, Franceschi C, Gaettic R, Cavalierid E, Suzukid H: Metallothioneins/PARP-1/IL-6 interplay on natural killer cell activity in elderly: parallelism with nonagenarians and old infected humans. Effect of zinc supply. Mech Ageing Dev. 2003, 124Google Scholar
- Mariani E, Ravaglia G, Forti P, Meneghetti A, Tarozzi A, Maioli F, Boschi F, Pratelli L, Pizzoferrato A, Piras F, Facchini A: Vitamin D, thyroid hormones and muscle mass influence natural killer (NK) innate immunity in healthy nonagenarians and centenarians. Clin Exp Immunol. 1999, 116: 19-27. 10.1046/j.1365-2249.1999.00855.x.PubMedPubMed CentralGoogle Scholar
- Sheikh A, Shamsuzzaman S, Ahmad SM, Nasrin D, Nahar S, Alam MM, Al Tarique A, Begum YA, Qadri SS, Chowdhury MI, Saha A, Larson CP, Qadri F: Zinc Influences the Innate Immune Responses in Children with Enterotoxigenic Escherichia coli-Induced Diarrhea. J Nutr. 2010, 140 (5): 1049-56. 10.3945/jn.109.111492.PubMedGoogle Scholar
- Cipriano C, Malavolta M, Costarelli L, Giacconi R, Muti E, Gasparini N, Cardelli M, Monti D, Mariani E, Mocchegiani E: Polymorphisms in MT1a gene coding region are associated with longevity in Italian Central female population. Biogerontology. 2006, 7: 357-365. 10.1007/s10522-006-9050-x.PubMedGoogle Scholar
- Taniguchi M, Seino K, Nakayama T: The NKT cell system: bridging innate and acquired immunity. Nat Immunol. 2003, 4: 1164-1165. 10.1038/ni1203-1164.PubMedGoogle Scholar
- Davis SR, Cousins RJ: Metallothionein expression in animals: a physiological perspective on function. J Nutr. 2000, 13: 1085-1088.Google Scholar
- Mocchegiani E, Giacconi R, Muti E, Cipriano C, Costarelli L, Tesei S: Zinc-bound metallothioneins and immune plasticity: lessons from very old mice and humans. Immun Ageing. 2007, 4: 1-7. 10.1186/1742-4933-4-1.Google Scholar
- Kovalovsky D, Uche OU, Eladad S, Hobbs RM, Yi W, Alonzo E, Chua K, Eidson M, Kim H-J, Im JS, Pandolfi PP, Sant'Angelo DB: The BTB-zinc finger transcriptional regulator, PLZF, controls the development of iNKT cell effector functions. Nat Immunol. 2008, 9: 1055-1064. 10.1038/ni.1641.PubMedPubMed CentralGoogle Scholar
- Mocchegiani E, Giacconi R, Cipriano C, Malavolta M: NK and NKT Cells in Aging and Longevity: Role of Zinc and Metallothioneins. Journal of Clinical Immunology. 2009, 29: 416-425. 10.1007/s10875-009-9298-4.PubMedGoogle Scholar
- Kitamura H, Morikawa H, Kamon H, Iguchi M, Hojyo S, Fukada T, Yamashita S, Kaisho T, Akira S, Murakami M, Hirano T: Toll-like receptor-mediated regulation of zinc homeostasis influences dendritic cell function. Nat Immunol. 2006, 7: 971-977. 10.1038/ni1373.PubMedGoogle Scholar
- Yamasaki S, Sakata-Sogawa K, Hasegawa A, Suzuki T, Kabu K, Sato E, Kurosaki T, Yamashita S, Tokunaga M, Nishida K, Hirano T: Zinc is a novel intracellular second messenger. J Cell Biol. 2007, 177: 637-645. 10.1083/jcb.200702081.PubMedPubMed CentralGoogle Scholar
- Kabu K, Yamasaki S, Kamimura D, Ito Y, Hasegawa A, Sato E, Kitamura H, Nishida K, Hirano T: Zinc is required for Fc epsilon RI-mediated mast cell activation. J Immunol. 2006, 177 (2): 1296-305.PubMedGoogle Scholar
- Sugiura T, Kuroda E, UY : Dysfunction of macrophages in metallothioneinknock out mice. J UOEH. 2004, 26: 193-205.PubMedGoogle Scholar
- Wellinghausen N, Kirchner H, Rink L: The immunobiology of zinc. Immunol Today. 1997, 18: 519-521. 10.1016/S0167-5699(97)01146-8.PubMedGoogle Scholar
- Bao B, Prasad AS, Beck FW, Godmere M: Zinc modulates mRNA levels of cytokines. Am J Physiol Endocrinol Metab. 2003, 285: E1095-1102.PubMedGoogle Scholar
- Zhou Z, Wang L, Song Z, Saari JT, McClain CJ, Kang YJ: Abrogation of nuclear factor-kappaB activation is involved in zinc inhibition of lipopolysaccharide-induced tumor necrosis factor-alpha production and liver injury. Am J Pathol. 2004, 164: 1547-1556.PubMedPubMed CentralGoogle Scholar
- Murakami M, Hirano T: Intracellular zinc homeostasis and zinc signaling. Cancer Sci. 2008, 99: 1515-1522. 10.1111/j.1349-7006.2008.00854.x.PubMedGoogle Scholar
- Knoell DL, Julian MW, Bao S, Besecker B, Macre JE, Leikauf GD, DiSilvestro RA, Crouser ED: Zinc deficiency increases organ damage and mortality in a murine model of polymicrobial sepsis. Crit Care Med. 2009, 37 (4): 1380-8. 10.1097/CCM.0b013e31819cefe4.PubMedPubMed CentralGoogle Scholar
- Zalewski PD: Zinc metabolism in the airway: basic mechanisms and drug targets. Curr Opin Pharmacol. 2006, 6 (3): 237-43. 10.1016/j.coph.2006.01.005.PubMedGoogle Scholar
- Mulay IL, Roy R, Knox BE, Suhr NH, Delaney WE: Trace-metal analysis of cancerous and noncancerous human tissues. J Natl Cancer Inst. 1971, 47: 1-13.PubMedGoogle Scholar
- Schlag P, Seeling W, Merkle P, Betzler M: Changes of serum-zinc in breast cancer. Langenbecks Arch Chir. 1978, 2: 129-133. 10.1007/BF01261399.Google Scholar
- Gupta SK, Singh SP, Shukla VK: Copper, zinc, and Cu/Zn ratio in carcinoma of the gallbladder. J Surg Oncol. 2005, 91: 204-208. 10.1002/jso.20306.PubMedGoogle Scholar
- Issell BF, Macfadyen BV, Gum ET, Valdivieso M, Dudrick SJ, Bodey GP: Serum zinc levels in lung cancer patients. Cancer. 2006, 47: 1845-1848. 10.1002/1097-0142(19810401)47:7<1845::AID-CNCR2820470721>3.0.CO;2-B.Google Scholar
- Büntzel J, Bruns F, Glatzel M, Garayev A, Mücke R, Kisters K, Schäfer U, Schönekaes K, Micke O: Zinc concentrations in serum during head and neck cancer progression. Anticancer Res. 2007, 27 (4A): 1941-3.PubMedGoogle Scholar
- Chakravarty PK, Ghosh A, Chowdhury JR: Zinc in human malignancies. Neoplasma. 1985, 33: 85-90.Google Scholar
- Schwartz M: Role of trace elements in cancer. Cancer Res. 1975, 35: 3481-3487.PubMedGoogle Scholar
- Margalioth EJ, Schenker JG, Chevion M: Copper and zinc levels in normal and malignant tissues. Cancer Sci. 1983, 52: 868-872.Google Scholar
- Costello LC, Franklin RB: The clinical relevance of the metabolism of prostate cancer; zinc and tumor suppression: connecting the dots. Mol Cancer. 2006, 5: 17-10.1186/1476-4598-5-17.PubMedPubMed CentralGoogle Scholar
- Gonzalez A, Peters U, Lampe JW, White E: Zinc intake from supplements and diet and prostate cancer. Nutr Cancer. 2009, 61 (2): 206-15. 10.1080/01635580802419749.PubMedPubMed CentralGoogle Scholar
- Jayaraman AK, Jayaraman S: Increased level of exogenous zinc induces cytotoxicity and up-regulates the expression of the ZnT-1 zinc transporter gene in pancreatic cancer cells. J Nutr Biochem. 2010, In Press Corrected Proof, Available online 14 April 2010Google Scholar
- Cho YS, Lee KH, Park JW: Pyrithione-zinc Prevents UVB-induced Epidermal Hyperplasia by Inducing HIF-1alpha. Korean J Physiol Pharmacol. 2010, 14 (2): 91-7. 10.4196/kjpp.2010.14.2.91.PubMedPubMed CentralGoogle Scholar
- Marks PA: Histone deacetylase inhibitors: A chemical genetics approach to understanding cellular functions. Biochim Biophys Acta. 2010, In press corrected proof, Available online 8 June 2010Google Scholar
- Yamashita S, Miyagi C, Fukada T, Kagara N, Che YS, Hirano T: Zinc transporter LIVI controls epithelial-mesenchymal transition in zebrafish gastrula organizer. Nature. 2004, 429 (6989): 298-302. 10.1038/nature02545.PubMedGoogle Scholar
- Cano A, Pérez-Moreno MA, Rodrigo I, Locascio A, Blanco MJ, del Barrio MG, Portillo F, Nieto MA: The transcription factor Snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression. Nat Cell Biol. 2002, 2 (2): 76-83. 10.1038/35000025.Google Scholar
- Guaita S, Puig I, Franci C, Garrido M, Dominguez D, Batlle E, Sancho E, Dedhar S, De Herreros AG, Baulida J: Snail induction of epithelial to mesenchymal transition in tumor cells is accompanied by MUC1 repression and ZEB1 expression. J Biol Chem. 2002, 277 (42): 39209-16. 10.1074/jbc.M206400200.PubMedGoogle Scholar
- Ibs KH, Rink L: Zinc-altered immune function. J Nutr. 2003, 133 (5 Suppl 1): 1452-6.Google Scholar
- Frederickson CJ: Neurobiology of zinc and zinc-containing neurons. Int Rev Neurobiol. 1989, 31: 145-238. full_text.PubMedGoogle Scholar
- Eide D: The SLC39 family of metal ion transporters. Pflugers Arch. 2004, 447: 796-800. 10.1007/s00424-003-1074-3.PubMedGoogle Scholar
- Gaither LA, Eide DJ: The human ZIP1 transporter mediates zinc uptake in human K562 erythroleukemia cells. J Biol Chem. 2001, 276: 22258-22264. 10.1074/jbc.M101772200.PubMedGoogle Scholar
- Palmiter RD, Huang L: Efflux and compartmentalization of zinc by members of the SLC30 family of solute carriers. Pflugers Arch. 2004, 447: 744-751. 10.1007/s00424-003-1070-7.PubMedGoogle Scholar
- Liuzzi JP, Cousins RJ: Mammalian zinc transporters. Annu Rev Nutr. 2004, 24: 151-172. 10.1146/annurev.nutr.24.012003.132402.PubMedGoogle Scholar
- Kambe T, Yamaguchi-Iwai Y, Sasaki R, Nagao M: Overview of mammalian zinc transporters. Cell Mol Life Sci. 2004, 1: 49-68. 10.1007/s00018-003-3148-y.Google Scholar
- Albrecht AL, Somji S, Sens MA, Sens DA, Garrett SH: Zinc transporter mRNA expression in the RWPE-1 human prostate epithelial cell line. Biometals. 2008, 4: 405-416. 10.1007/s10534-007-9129-0.Google Scholar
- Lichten LA, Cousins RJ: Mammalian zinc transporters: nutritional and physiological regulation. Annu Rev Nutr. 2009, 29: 152-176. 10.1146/annurev-nutr-033009-083312.Google Scholar
- Taylor KM: A distinct role in breast cancer for two LIV-1 family zinc transporters. Biochem Soc Trans. 2008, 36 (Pt 6): 1247-1251. 10.1042/BST0361247.PubMedGoogle Scholar
- Li M, Zhang Y, Liu Z, Bharadwaj U, Wang H, Wang X, Zhang S, Liuzzi JP, Chang SM, Cousins RJ, Fisher WE, Brunicardi FC, Logsdon CD, Chen C, Yao Q: Aberrant expression of zinc transporter ZIP4 (SLC39A4) significantly contributes to human pancreatic cancer pathogenesis and progression. Proc Natl Acad Sci USA. 2007, 47: 18636-18641. 10.1073/pnas.0709307104.Google Scholar
- Eide D, Broderius M, Fett J, Guerinot ML: A novel iron-regulated metal transporter from plants identified by functional expression in yeast. Proc Natl Acad Sci USA. 1996, 1996: 5624-5628. 10.1073/pnas.93.11.5624.Google Scholar
- Zhao H, Eide D: The yeast ZRT1 gene encodes the zinc transporter protein of a high-affinity uptake system induced by zinc limitation. Proc Natl Acad Sci USA. 1996, 93: 2454-2458. 10.1073/pnas.93.6.2454.PubMedPubMed CentralGoogle Scholar
- Truong-Tran AQ, Carter J, Ruffin RE, Zalewski PD: The role of zinc in caspase activation and apoptotic cell death. Biometals. 2001, 14: 315-330. 10.1023/A:1012993017026.PubMedGoogle Scholar
- Sun XM, MacFarlane M, Zhuang J, Wolf BB, Green DR, Cohen GM: Distinct caspase cascades are initiated in receptor-mediated and chemical-induced apoptosis. J Biol Chem. 1999, 274: 5053-5060. 10.1074/jbc.274.8.5053.PubMedGoogle Scholar
- Strasser A, O'Connor L, Dixit VM: Apoptosis signaling. Annu Rev Biochem. 2000, 69: 217-245. 10.1146/annurev.biochem.69.1.217.PubMedGoogle Scholar
- Song Z, Steller H: Death by design: mechanism and control of apoptosis. Trends Cell Biol. 1999, 9: 49-52. 10.1016/S0962-8924(99)01670-0.Google Scholar
- Thompson CB: Apoptosis in the pathogenesis and treatment of disease. Science. 1995, 267: 1456-1462. 10.1126/science.7878464.PubMedGoogle Scholar
- Wyllie AH: Apoptosis: an overview. Br Med Bull. 1997, 53: 451-465.PubMedGoogle Scholar
- Sensi SL, Rapposelli IG, Frazzini V, Mascetra N: Altered oxidant-mediated intraneuronal zinc mobilization in a triple transgenic mouse model of Alzheimer's disease. Exp Gerontol. 2008, 43 (5): 488-92. 10.1016/j.exger.2007.10.018.PubMedGoogle Scholar
- Maret W: Molecular aspects of human cellular zinc homeostasis: redox control of zinc potentials and zinc signals. Biometals. 2009, 22 (1): 149-57. 10.1007/s10534-008-9186-z.PubMedGoogle Scholar
- Shumilina E, Xuan NT, Schmid E, Bhavsar SK, Szteyn K, Gu S, Götz F, Lang F: Zinc induced apoptotic death of mouse dendritic cells. Apoptosis. 2010, 15 (10): 1177-86. 10.1007/s10495-010-0520-x.PubMedGoogle Scholar
- Kiedaisch V, Akel A, Niemoeller OM, Wieder T, Lang F: Zinc-induced suicidal erythrocyte death. Am J Clin Nutr. 2008, 87 (5): 1530-4.PubMedGoogle Scholar
- Sensi SL, Yin HZ, Carriedo SG, Rao SS, Weiss JH: Preferential Zn2+ influx through Ca2+ -permeable AMPA/kainate channels triggers prolonged mitochondrial superoxide production. Proc Natl Acad Sci USA. 1999, 96: 2414-2419. 10.1073/pnas.96.5.2414.PubMedPubMed CentralGoogle Scholar
- Hamatake M, Iguchi K, Hirano K, Ishida R: Zinc Induces Mixed Types of Cell Death, Necrosis, and Apoptosis, in Molt-4 Cells. J Biochem. 2000, 128: 933-939.PubMedGoogle Scholar
- Untergasser G, Rumpold H, Plas E, Witkowski M, Pfister G, Berger P: High Levels of Zinc Ions Induce Loss of Mitochondrial Potential and Degradation of Anti-apoptotic Bcl-2 Protein in in vitro Cultivated Human Prostate Epithelial Cells. Biochem Biophys Res Commun. 2000, 279: 607-614. 10.1006/bbrc.2000.3975.PubMedGoogle Scholar
- Bozym RA, Chimienti F, Giblin LJ, Gross GW, Korichneva I, Li Y, Libert S, Maret W, Parviz M, Frederickson CJ, Thompson RB: Free zinc ions outside a narrow concentration range are toxic to a variety of cells in vitro. Exp Biol Med. 2010, 235 (6): 741-50. 10.1258/ebm.2010.009258.Google Scholar
- Truong-Tran AQ, Ho LH, Chai F, Zalewski PD: Cellular zinc fluxes and the regulation of apoptosis/gene-directed cell death. J Nutrition. 2000, 130 (Suppl): 1459-1466.Google Scholar
- Adamo AM, Zago MP, Mackenzie GG, Aimo L, Keen CL, Keenan A, Oteiza PI: The role of zinc in the modulation of neuronal proliferation and apoptosis. Neurotox Res. 2010, 17 (1): 1-14. 10.1007/s12640-009-9067-4.PubMedPubMed CentralGoogle Scholar
- Chai F, Truong-Tran AQ, Evdokiou A, Young GP, Zalewski PD: Intracellular Zinc Depletion Induces Caspase Activation and p21Waf1/Cip1 Cleavage in Human Epithelial Cell Lines. J Infect Diseases. 2000, 182: S85-S92. 10.1086/315914.Google Scholar
- Duvall E, Wyllie AH: Death and the cell. Immunol Today. 1986, 7: 115-119. 10.1016/0167-5699(86)90152-0.PubMedGoogle Scholar
- Zalewski PD, Forbes IJ: Intracellular zinc and the regulation of apoptosis. Programmed Cell Death: The Cellular and Molecular Biology of Apoptosis. Edited by: Lavin M, Watters D. 1993, Melbourne: Harwood Academic PublishersGoogle Scholar
- Rogers JM, Taubeneck MW, Daston GP, Sulik KK, Zucker RM, Elstein KH, Jankowski MA, Keen CL: Zinc deficiency causes apoptosis but not cell cycle alterations in organogenesis-stage rat embryos: effect of varying duration of deficiency. Teratology. 1995, 52: 149-159. 10.1002/tera.1420520307.PubMedGoogle Scholar
- Franklin RB, Costello LC: The important role of the apoptotic effects of zinc in the development of cancers. Journal of Cellular Biochemistry. 2009, 106: 750-757. 10.1002/jcb.22049.PubMedPubMed CentralGoogle Scholar
- Peterson QP, Goode DR, West CW, Ramsey KN, Lee JJY, Hergenrother PJ: PAC-1 activates procaspase-3 in vitro through relief of zinc-mediated inhibition. J Mol Biol. 2009, 388: 144-158. 10.1016/j.jmb.2009.03.003.PubMedPubMed CentralGoogle Scholar
- Oteiza PI, Olin KL, Fraga CG, Keen CL: Zinc deficiency causes oxidative damage to proteins, lipids and DNA in rat testes. J Nutr. 1995, 125: 823-829.PubMedGoogle Scholar
- Taylor CG, Towner RA, Janzen EG, Bray TM: MRI detection of hyperoxiainduced lung edema in Zn deficient rats. Free Radic Biol Med. 1990, 9: 229-233. 10.1016/0891-5849(90)90033-F.PubMedGoogle Scholar
- Kraus A, Roth HP, Kirchgessner M: Supplementation with vitamin C, vitamin E or beta-carotene influences osmotic fragility and oxidative damage of erythrocytes of zinc-deficient rats. J Nutr. 1997, 127: 1290-1296.PubMedGoogle Scholar
- Zalewski PD, Forbes IJ, Betts WH: Correlation of apoptosis with change in intracellular labile Zn, using Zinquin, a new specific fluorescent probe for zinc. Biochem J. 1993, 296: 403-408.PubMedPubMed CentralGoogle Scholar
- Meerarani P, Ramadass P, Toborek M, Bauer HC, Bauer H, Hennig B: Zinc protects against apoptosis of endothelial cells induced by linoleic acid and tumor necrosis factor alpha. Am J Clin Nutr. 2000, 71: 81-87.PubMedGoogle Scholar
- Vallee BL, Falchuk KH: The biochemical basis of zinc physiology. Physiol Rev. 1993, 79-118.Google Scholar
- Yang Y, Kawataki T, Fukui K, Koike T: Cellular Zn2+ chelators cause "dying-back" neurite degeneration associated with energy impairment. J Neurosci Res. 2007, 85 (13): 2844-55. 10.1002/jnr.21411.PubMedGoogle Scholar
- Baird SK, Kurz T, Brunk UT: Metallothionein protects against oxidative stress-induced lysosomal destabilization. Biochem J. 2006, 394 (Pt 1): 275-83.PubMedPubMed CentralGoogle Scholar
- Williams RJP: The biochemistry of zinc. Polyhedron. 1987, 6: 61-69. 10.1016/S0277-5387(00)81239-5.Google Scholar
- Roychowdhury M, Sarkar N, Manna T, Bhattacharyya S, Sarkar T, Basusarkar P, Roy S, Bhattacharyya B: Sulfhydryls of tubulin: A probe to detect conformational changes of tubulin. Eur J Biochem. 2000, 267: 3469-3476. 10.1046/j.1432-1327.2000.01369.x.PubMedGoogle Scholar
- Hesketh JE: Zinc-stimulated microtubule assembly and evidence for zinc binding to tubulin. Int J Biochem. 1982, 14: 983-990. 10.1016/0020-711X(82)90059-3.PubMedGoogle Scholar
- Banan A, Fields JZ, Decker H, Zhang Y, Keshavarzian A: Nitric oxide and its metabolites mediate ethanol-induced microtubule disruption and intestinal barrier dysfunction. J Pharmacol Exp Ther. 2000, 294: 997-1008.PubMedGoogle Scholar
- Martin SJ, Cotter TG: Specific loss of microtubules in HL-60 cells leads to programmed cell death (apoptosis). Biochem Soc Trans. 1990, 18: 299-301.PubMedGoogle Scholar
- Bozym RA, Thompson RB, Stoddard AK, Fierke CA: Measuring picomolar intracellular exchangeable zinc in PC-12 cells using a ratiometric fluorescence biosensor. ACS Chem Biol. 2006, 1 (2): 103-11. 10.1021/cb500043a.PubMedGoogle Scholar
- Floersheim GL, Christ A, Koenig R, Racine C, Gudat F: Radiation-induced lymphoid tumors and radiation lethality are inhibited by combined treatment with small doses of zinc aspartate and WR 2721. Int J Cancer. 1992, 52: 604-608. 10.1002/ijc.2910520419.PubMedGoogle Scholar
- Matsushita K, Kitagawa K, Matsuyama T, Ohtsuki T, Taguchi A, Mandai K, Mabuchi T, Yagita Y, Yanagihara T, Matsumoto M: Effect of systemic zinc administration on delayed neuronal death in the gerbil hippocampus. Brain Res. 1996, 743: 362-365. 10.1016/S0006-8993(96)01112-2.PubMedGoogle Scholar
- Kuo IC, Seitz B, LaBree L, McDonnell PJ: Can zinc prevent apoptosis of anterior keratocytes after superfcial keratectomy. Cornea. 1997, 16: 550-555. 10.1097/00003226-199709000-00011.PubMedGoogle Scholar
- Sankaramanivel S, Rajaram A, Rajaram R: Zinc protects human peripheral blood lymphocytes from Cr(III)(phenanthroline)3-induced apoptosis. Toxicol Appl Pharmacol. 2010, 243 (3): 405-19. 10.1016/j.taap.2009.12.018.PubMedGoogle Scholar
- Sunderman FW: The influence of zinc on apoptosis. Ann Clin Lab Sci. 1995, 25: 134-142.PubMedGoogle Scholar
- Raymond AD, Gekonge B, Giri MS, Hancock A, Papasavvas E, Chehimi J, Kossevkov AV, Nicols C, Yousef M, Mounzer K, Shull J, Kostman J, Showe L, Montaner LJ: Increased metallothionein gene expression, zinc, and zinc-dependent resistance to apoptosis in circulating monocytes during HIV viremia. J Leukoc Biol. 2010, 88 (3): 589-96. 10.1189/jlb.0110051.PubMedPubMed CentralGoogle Scholar
- Zalewski PD, Forbes IJ, Giannakis C: Physiological role for zinc in prevention of apoptosis (gene-directed death). Biochem Inter. 1991, 24: 1093-1101.Google Scholar
- Kolenko V, Uzzo RG, Bukowski R, Bander NH, Novick AC, His ED, Finke JH: Dead or dying: necrosis versus apoptosis in caspase-deficient human renal cell carcinoma. Cancer Res. 1999, 59: 2838-2842.PubMedGoogle Scholar
- Yorimitsu T, Klionsky DJ: Autophagy: molecular machinery for self-eating. Cell Death Differ. 2005, 12 (Suppl2): 1542-1552. 10.1038/sj.cdd.4401765.PubMedPubMed CentralGoogle Scholar
- Majeski AE, Dice JF: Mechanisms of chaperone-mediated autophagy. Int J Biochem Cell Biol. 2004, 36: 2435-2444. 10.1016/j.biocel.2004.02.013.PubMedGoogle Scholar
- Massey A, Kiffin R, Cuervo AM: Pathophysiology of chaperone-mediated autophagy. Int J Biochem Cell Biol. 2004, 36: 2420-2434. 10.1016/j.biocel.2004.04.010.PubMedGoogle Scholar
- Reggiori F, Klionsky DJ: Autophagy in the eukaryotic cell. Eukaryot Cell. 2002, 1: 11-21. 10.1128/EC.01.1.11-21.2002.PubMedPubMed CentralGoogle Scholar
- Wang C-W, Klionsky DJ: The molecular mechanism of autophagy. Mol Med. 2003, 9: 65-76.PubMedPubMed CentralGoogle Scholar
- Kuma A, Hatano M, Matsui M, Yamamoto A, Nakaya H, Yoshimori T, Ohsumi Y, Tokuhisa T, Mizushima N: The role of autophagy during the early neonatal starvation period. Nature. 2004, 432: 1032-1036. 10.1038/nature03029.PubMedGoogle Scholar
- Mizushima N, Yamamoto A, Matsui M, Yoshimori T, Ohsumi Y: vivo analysis of autophagy in response to nutrient starvation using transgenic mice expressing a fluorescent autophagosome marker. Mol Biol Cell. 2004, 15: 1101-1111. 10.1091/mbc.E03-09-0704.PubMedPubMed CentralGoogle Scholar
- Levine B, Klionsky DJ: Development by self-digestion: molecular mechanisms and biological functions of autophagy. Dev Cell. 2004, 6: 463-477. 10.1016/S1534-5807(04)00099-1.PubMedGoogle Scholar
- Cuervo AM: Autophagy: in sickness and in health. Trends Cell Biol. 2004, 14: 70-77. 10.1016/j.tcb.2003.12.002.PubMedGoogle Scholar
- Shintani T, Klionsky DJ: Autophagy in health and disease: a double-edged sword. Science. 2004, 306: 990-995. 10.1126/science.1099993.PubMedPubMed CentralGoogle Scholar
- Kirkegaard K, Taylor MP, Jackson WT: Cellular autophagy: surrender, avoidance and subversion by microorganisms. Nat Rev Microbiol. 2004, 2: 301-314. 10.1038/nrmicro865.PubMedGoogle Scholar
- Levine B: Eating oneself and uninvited guests: autophagy-related pathways in cellular defense. Cell. 2005, 120: 159-162.PubMedGoogle Scholar
- Bursch W: Multiple cell death programs: Charon's lifts to Hades. FEMS Yeast Res. 2004, 5: 101-110. 10.1016/j.femsyr.2004.07.006.PubMedGoogle Scholar
- Lee SJ, Cho KS, Koh JY: Oxidative injury triggers autophagy in astrocytes: the role of endogenous zinc. Glia. 2009, 57: 351-361. 10.1002/glia.20763.Google Scholar
- Chung H, Yoon YH, Hwang JJ, Cho KS, Koh JY, Kim JG: Ethambutol-induced toxicity is mediated by zinc and lysosomal membrane permeabilization in cultured retinal cells. Toxicol Appl Pharmacol. 2009, 235: 163-170. 10.1016/j.taap.2008.11.006.PubMedGoogle Scholar
- Iwanyshyn WM, Han GS, Carman GM: Regulation of phospholipid synthesis in Saccharomyces cerevisiae by zinc. J Biol Chem. 2004, 279 (21): 21976-83. 10.1074/jbc.M402047200.PubMedGoogle Scholar
- Hwang JJ, Kim HN, Kim J, Cho DH, Kim MJ, Kim YS, Kim Y, Park SJ, Koh JY: Zinc(II) ion mediates tamoxifen-induced autophagy and cell death in MCF-7 breast cancer cell line. Biometals. 2010, 23 (6): 997-1013. 10.1007/s10534-010-9346-9.PubMedGoogle Scholar
- Hwang JJ, Lee SJ, Kim TY, Cho JH, Koh JY: Zinc and 4-hydroxy-2-nonenal mediate lysosomal membrane permeabilization induced by H2O2 in cultured hippocampal neurons. J Neurosci. 2008, 28 (12): 3114-22. 10.1523/JNEUROSCI.0199-08.2008.PubMedGoogle Scholar
- Lee SJ, Park MH, Kim HJ, Koh JY: Metallothionein-3 regulates lysosomal function in cultured astrocytes under both normal and oxidative conditions. Glia. 2010, 58 (10): 1186-96.PubMedGoogle Scholar
- Lee HK, Mattei LM, Steinberg BE, Alberts P, Lee YH, Chervonsky A, Mizushima N, Grinstein S, Iwasaki A: In vivo requirement for Atg5 in antigen presentation by dendritic cells. Immunity. 2010, 32 (2): 227-39. 10.1016/j.immuni.2009.12.006.PubMedPubMed CentralGoogle Scholar
- Sparvero LJ, Asafu-Adjei D, Kang R, Tang D, Amin N, Im J, Rutledge R, Lin B, Amoscato AA, Zeh HJ, Lotze MT: RAGE (Receptor for Advanced Glycation Endproducts), RAGE ligands, and their role in cancer and inflammation. J Transl Med. 2009, 17-10.1186/1479-5876-7-17.Google Scholar
- Lotze MT, Tracey KJ: High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenal. Nat Rev Immunol. 2005, 5: 331-342. 10.1038/nri1594.PubMedGoogle Scholar
- Tang DL, Kang R, Zeh HJ, Lotze MT: HMGB1 and Cancer. Biochim Biophys Acta. 2010, 1799 (1-2): 131-40.PubMedPubMed CentralGoogle Scholar
- Prasad AS: Effects of zinc deficiency on Th1 and Th2 cytokine shifts. J Infect Dis. 2000, 2182 (Suppl 1): 62-68. 10.1086/315916.Google Scholar
- Tanaka S, Akaishi E, Hosaka K, Okamura S, Kubohara Y: Zinc ions suppress mitogen-activated interleukin-2 production in Jurkat cells. Biochem Biophys Res Commun. 2005, 335 (1): 162-7. 10.1016/j.bbrc.2005.07.059.PubMedGoogle Scholar
- Wu W, Silbajoris RA, Cao D, Bromberg PA, Zhang Q, Peden DB, Samet JM: Regulation of cyclooxygenase-2 expression by cAMP response element and mRNA stability in a human airway epithelial cell line exposed to zinc. Toxicol Appl Pharmacol. 2008, 231 (2): 260-6. 10.1016/j.taap.2008.04.012.PubMedGoogle Scholar
- Shen H, Oesterling E, Stromberg A, Toborek M, MacDonald R, Hennig B: Zinc deficiency induces vascular pro-inflammatory parameters associated with NF-kappaB and PPAR signaling. J Am Coll Nutr. 2008, 27 (5): 577-87.PubMedGoogle Scholar
- Yamaki K, Yoshino S: Comparison of inhibitory activities of zinc oxide ultrafine and fine particulates on IgE-induced mast cell activation. Biometals. Available online, 2009 Jul 17,Google Scholar
- Putics A, Vödrös D, Malavolta M, Mocchegiani E, Csermely P, Soti C: Zinc supplementation boosts the stress response in the elderly: Hsp70 status is linked to zinc availability in peripheral lymphocytes. Exp Gerontol. 2008, 43 (5): 452-61. 10.1016/j.exger.2008.01.002.PubMedGoogle Scholar
- Safieh-Garabedian B, Poole S, Allchorne A, Kanaan S, Saade N, Woolf CJ: Zinc reduces the hyperalgesia and upregulation of NGF and IL-1 beta produced by peripheral inflammation in the rat. Neuropharmacology. 1996, 35 (5): 599-603. 10.1016/0028-3908(96)84630-2.PubMedGoogle Scholar
- Aydemir TB, Liuzzi JP, McClellan S, Cousins RJ: Zinc transporter ZIP8 (SLC39A8) and zinc influence IFN-gamma expression in activated human T cells. J Leukoc Biol. 2009, 86 (2): 337-48. 10.1189/jlb.1208759.PubMedPubMed CentralGoogle Scholar
- Bao B, Prasad A, Beck FW, Suneja A, Sarkar F: Toxic effect of zinc on NF-kappaB, IL-2, IL-2 receptor alpha, and TNF-alpha in HUT-78 (Th(0)) cells. Toxicol Lett. 2006, 166 (3): 222-8. 10.1016/j.toxlet.2006.07.306.PubMedGoogle Scholar
- Mariani E, Neri S, Cattini L, Mocchegiani E, Malavolta M, Dedoussis GV, Kanoni S, Rink L, Jajte J, Facchini A: Effect of zinc supplementation on plasma IL-6 and MCP-1 production and NK cell function in healthy elderly: interactive influence of +647 MT1a and -174 IL-6 polymorphic alleles. Exp Gerontol. 2008, 43 (5): 462-71. 10.1016/j.exger.2007.12.003.PubMedGoogle Scholar
- Giacconi R, Cipriano C, Muti E, Costarelli L, Maurizio C, Saba V, Gasparini N, Malavolta M, Mocchegiani E: Novel -209A/G MT2A polymorphism in old patients with type 2 diabetes and atherosclerosis: relationship with inflammation (IL-6) and zinc. Biogerontology. 2005, 6 (6): 407-13. 10.1007/s10522-005-4907-y.PubMedGoogle Scholar
- Rajagopalan S, Winter CC, Wagtmann N, Long EO: The Ig-related killer cell inhibitory receptor binds zinc and requires zinc for recognition of HLA-C on target cells. J Immunol. 1995, 155 (9): 4143-6.PubMedGoogle Scholar
- Valés-Gómez M, Erskine RA, Deacon MP, Strominger JL, Reyburn HT: The role of zinc in the binding of killer cell Ig-like receptors to class I MHC proteins. Proc Natl Acad Sci USA. 2001, 98 (4): 1734-9. 10.1073/pnas.041618298.PubMedPubMed CentralGoogle Scholar
- Li Y, Li H, Dimasi N, McCormick JK, Martin R, Schuck P, Schlievert PM, Mariuzza RA: Crystal structure of a superantigen bound to the high-affinity, zinc-dependent site on MHC class II. Immunity. 2001, 14 (1): 93-104. 10.1016/S1074-7613(01)00092-9.PubMedGoogle Scholar
- Roussel A, Anderson BF, Baker HM, Fraser JD, Baker EN: Crystal structure of the streptococcal superantigen SPE-C: dimerization and zinc binding suggest a novel mode of interaction with MHC class II molecules. Nat Struct Biol. 1997, 4 (8): 635-43. 10.1038/nsb0897-635.PubMedGoogle Scholar
- Prasad AS, Bao B, Beck FW, Sarkar FH: Zinc activates NF-kappaB in HUT-78 cells. J Lab Clin Med. 2001, 138 (4): 250-6. 10.1067/mlc.2001.118108.PubMedGoogle Scholar
- Shifera AS, Horwitz MS: Mutations in the zinc finger domain of IKK gamma block the activation of NF-kappa B and the induction of IL-2 in stimulated T lymphocytes. Mol Immunol. 2008, 45 (6): 1633-45. 10.1016/j.molimm.2007.09.036.PubMedGoogle Scholar
- Kim I, Kim CH, Kim JH, Lee J, Choi JJ, Chen ZA, Lee MG, Chung KC, Hsu CY, Ahn YS: Pyrrolidine dithiocarbamate and zinc inhibit proteasome-dependent proteolysis. Exp Cell Res. 2004, 298 (1): 229-38. 10.1016/j.yexcr.2004.04.017.PubMedGoogle Scholar
- Jarrousse V, Castex-Rizzi N, Khammari A, Charveron M, Dréno B: Zinc salts inhibit in vitro Toll-like receptor 2 surface expression by keratinocytes. Eur J Dermatol. 2007, 17 (6): 492-6.PubMedGoogle Scholar
- O'Reilly SM, Moynagh PN: Regulation of Toll-like receptor 4 signalling by A20 zinc finger protein. Biochem Biophys Res Commun. 2003, 303 (2): 586-93. 10.1016/S0006-291X(03)00389-9.PubMedGoogle Scholar
- Zhang W, Mi J, Li N, Sui L, Wan T, Zhang J, Chen T, Cao X: Identification and characterization of DPZF, a novel human BTB/POZ zinc finger protein sharing homology to BCL-6. Biochem Biophys Res Commun. 2001, 282 (4): 1067-73. 10.1006/bbrc.2001.4689.PubMedGoogle Scholar
- Sharif-Askari E, Vassen L, Kosan C, Khandanpour C, Gaudreau MC, Heyd F, Okayama T, Jin J, Rojas ME, Grimes HL, Zeng H, Möröy T: Zinc finger protein Gfi1 controls the endotoxin-mediated Toll-like receptor inflammatory response by antagonizing NF-kappaB p65. Mol Cell Biol. 2010, 30 (16): 3929-42. 10.1128/MCB.00087-10.PubMedPubMed CentralGoogle Scholar
- Jin J, Zeng H, Schmid KW, Toetsch M, Uhlig S, Möröy T: The zinc finger protein Gfi1 acts upstream of TNF to attenuate endotoxin-mediated inflammatory responses in the lung. Eur J Immunol. 2006, 36 (2): 421-30. 10.1002/eji.200535155.PubMedGoogle Scholar
- Lademann U, Kallunki T, Jäättelä M: A20 zinc finger protein inhibits TNF-induced apoptosis and stress response early in the signaling cascades and independently of binding to TRAF2 or 14-3-3 proteins. Cell Death Differ. 2001, 8 (3): 265-72. 10.1038/sj.cdd.4400805.PubMedGoogle Scholar
- Hong JW, Allen CE, Wu LC: Inhibition of NF-kappaB by ZAS3, a zinc-finger protein that also binds to the kappaB motif. Proc Natl Acad Sci USA. 2003, 100 (21): 12301-6. 10.1073/pnas.2133048100.PubMedPubMed CentralGoogle Scholar
- Lin LC, Que J, Lin KL, Leung HW, Lu CL, Chang CH: Effects of zinc supplementation on clinical outcomes in patients receiving radiotherapy for head and neck cancers: a double-blinded randomized study. Int J Radiat Oncol Biol Phys. 2008, 70 (2): 368-73. 10.1016/j.ijrobp.2007.06.073.PubMedGoogle Scholar
- Yamaguchi S: Subtraction cloning of growth arrest inducible genes in normal human epithelial cells. Kokubyo Gakkai Zasshi. 1995, 62: 78-93.PubMedGoogle Scholar
- Desouki MM, Geradts J, Milon B, Franklin RB, Costello LC: hZip2 and hZip3 zinc transporters are down regulated in human prostate adenocarcinomatous glands. Mol Cancer. 2007, 6: 37-10.1186/1476-4598-6-37.PubMedPubMed CentralGoogle Scholar
- Kagara N, Tanaka N, Noguchi S, Hirano T: Zinc and its transporter ZIP10 are involved in invasive behavior of breast cancer cells. Cancer Sci. 2007, 5: 692-697. 10.1111/j.1349-7006.2007.00446.x.Google Scholar
- Cousins RJ, Liuzzi JP, Lichten LA: Mammalian zinc transport, trafficking, and signals. J Biol Chem. 2006, 281: 24085-24089. 10.1074/jbc.R600011200.PubMedGoogle Scholar
- Taylor KM, Vichova P, Jordan N, Hiscox S, Hendley R, Nicholson RI: ZIP7 mediated intracellular zinc transport contributes to aberrant growth factor signaling in antihormone-resistant breast cancer Cells. Endocrinology. 2008, 149 (10): 4912-4920. 10.1210/en.2008-0351.PubMedGoogle Scholar
- Hogstrand C, Kille P, Nicholson RI, Taylor KM: Zinc transporters and cancer: a potential role for ZIP7 as a hub for tyrosine kinase activation. Trends Mol Med. 2009, 15 (3): 101-111. 10.1016/j.molmed.2009.01.004.PubMedGoogle Scholar
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