Differentiation of two types of mobilized peripheral blood stem cells by microRNA and cDNA expression analysis
© Jin et al; licensee BioMed Central Ltd. 2008
Received: 23 June 2008
Accepted: 22 July 2008
Published: 22 July 2008
Mobilized-peripheral blood hematopoietic stem cells (HSCs) have been used for transplantation, immunotherapy, and cardiovascular regenerative medicine. Agents used for HSC mobilization include G-CSF and the CXCR4 inhibitor AMD3100 (plerixafor). The HSCs cells mobilized by each agent may contain different subtypes and have different functions. To characterize mobilized HSCs used for clinical applications, microRNA (miRNA) profiling and gene expression profiling were used to compare AMD3100-mobilized CD133+ cells from 4 subjects, AMD3100 plus G-CSF-mobilized CD133+ cells from 4 subjects and G-CSF-mobilized CD34+ cells from 5 subjects. The HSCs were compared to peripheral blood leukocytes (PBLs) from 7 subjects.
Hierarchical clustering of miRNAs separated HSCs from PBLs. miRNAs up-regulated in all HSCs included hematopoiesis-associated miRNA; miR-126, miR-10a, miR-221 and miR-17-92 cluster. miRNAs up-regulated in PBLs included miR-142-3p, -218, -21, and -379. Hierarchical clustering analysis of miRNA expression separated the AMD3100-mobilized CD133+ cells from G-CSF-mobilized CD34+ cells. Gene expression analysis of the HSCs naturally segregated samples according to mobilization and isolation protocol and cell differentiation status.
HSCs and PBLs have unique miRNA and gene expression profiles. miRNA and gene expression microarrays maybe useful for assessing differences in HSCs.
Hematopoietic stem cells (HSCs) have been used for more than 35 years for transplantation therapy to treat acute and chronic leukemia, lymphoma, marrow failure and congenital immune deficiency. Advances in immunotherapy have lead to the use of HSCs to produce dendritic cells (DCs) to enhance antigen presentation , to enhance leukocyte recovery after immunosuppresive therapy, and to mount cancer rejection by adoptive transfer of tumor infiltrating lymphocytes (TIL) . HSCs have also been used to treat patients with ischemic cardiac disease to improve revascularization and cardiac function following acute myocardial ischemia [3, 4]. However, due to the diversity of stem cell sources, mobilization methods employed, purity of cells, and the content of cell subsets, there are many different types of HSCs and those that are most beneficial for one application may not be best for another.
HSCs can be obtained from several different sources including bone marrow, mobilized peripheral blood, and umbilical cord blood. For transplantation, traditionally, HSCs were obtained from the bone marrow. However, umbilical cord blood has been found to be especially rich in HSCs  and HSCs have been found in the peripheral blood and their level in the circulation increases several-fold after G-CSF administion [6, 7]. For HSC transplantation all three types of HSCs are used, but for most other applications mobilized peripheral blood HSCs are most commonly used.
The diversity of HSCs used for clinical therapies has also increased due to the development of new HSC mobilizing agents. For many years granulocyte colony-stimulating factor (G-CSF) has been the standard agent to increase the level of circulating HSCs. The administration of G-CSF daily for 4 to 6 days results in a 10- to 30-fold increase in the number of circulating HSCs [8, 9] and G-CSF-mobilized HSCs collected by apheresis have been used for transplantation, immune therapy and the treatment of cardiac ischemia. Another HSC mobilizing agent, AMD3100, has been used with G-CSF to mobilize stem cells for autologous transplants  and is currently being evaluated as a single agent to mobilize HSCs for allogeneic donor transplants [11, 12].
The mechanisms by which AMD3100 and G-CSF alter HSC trafficking and mobilization are different suggesting that HSCs with different intrinsic properties maybe be mobilized by these agents. AMD3100, as a CXCR4 antagonist, mobilizes HSCs within 6 hours by disrupting the engagement of stem cell surface CXCR4 with its ligand SDF-1 (CXCL12) which is expressed on marrow osteoblasts [10, 13–20]. In contrast G-CSF mobilizes stem cells indirectly by down regulating the expression of SDF-1 on marrow osteoblasts and by releasing neutrophil and monocyte proteolytic enzymes including neutrophil elastase, cathepsin G, and maxtrix metalloproteinase-9 which in turn degrade important HSC trafficking and adhesion molecules c-kit, VCAM-1, CXCR4, and SDF-1 . In animal studies AMD3100 mobilizes a CD34+ cell population with a greater long-term marrow repopulating capacity than G-CSF [12, 22, 23], possibly due to differences in mechanisms of mobilization.
Although commonly accepted HSC specific surface markers have been used for HSC characterization and purification, differences in the specificities of monoclonal antibodies used to isolate HSCs have contributed to diversity in HSC clinical products. Antibodies specific for CD34 have been the standard agent for the isolation of HSCs. In addition, anti-CD133 has also been used [24–27]. Approximately 75% of G-CSF mobilized peripheral blood stem cells (PBSCs) express CD34 as well as CD133, but small populations express one or the other .
MicroRNAs (miRNA) are short, 20–22 nucleotide long, RNA molecules which negatively regulate protein translation in a variety of biological processes, including developmental timing, signal transduction, tissue differentiation and stem cell renewal and differentiation. Some miRNAs are specifically expressed in stem cells and control stem cell self-renewal and differentiation by negatively regulating the expression of certain key genes in stem cells.
To determine if miRNA and gene expression profiling would be beneficial in distinguishing different types of HSCs, we compared CD133+ cells isolated from AMD3100- and AMD3100 plus G-CSF-mobilized PBSC concentrates with CD34+ cells isolated from G-CSF-mobilized PBSC concentrates. We applied miRNA profiling and gene expression profiling analysis to assess these three different types of progenitor cell populations using peripheral blood T cells, B cells, monocytes and NK cells as a reference. We hypothesized that miRNA and gene expression analysis would be useful for characterizing HSCs. Global gene and miRNA expression profiling was used to compare HSCs and peripheral blood leukocytes. T cells, B cells, monocytes and NK cells isolated from peripheral blood mononuclear cells (PBMCs) were compared to the HSCs.
Hematopoietic progenitor cell isolation
AMD3100 and AMD3100 plus G-CSF stem cell mobilization, collections and isolation
For the mobilization of cells with AMD3100 alone, one dose of AMD3100 (Plerixafor, Genzyme Corporation, Cambridge, MA) (240 μg/kg) was given subcutaneously and PBSC concentrate was collected by leukapheresis (CS3000, Baxter Healthcare Corp., Fenwal Division, Deerfield, IL) six hours later. For AMD3100 plus G-CSF-mobilization G-CSF (10 μg/kg) (Filgrastim, Amgen, Thousand Oaks, CA) was given subcutaneously to healthy subjects daily for four days and on the fifth day in addition to G-CSF, AMD3100 (240 μg/kg) was given subcutaneously. A mobilized PBSC concentrate was collected by leukapheresis (CS3000, Baxter Healthcare Corp.) on day 5 twelve hours after the administration of AMD3100 and 2 hours after the last dose of G-CSF. CD133+ cells were isolated from the PBSC concentrates by positive selection with anti-CD133 and magnetic microparticles (CliniMacs, Miltenyi Biotec, Bergisch Gladbach, Germany) and the isolated cells were cryopreserved. The proportion of isolated cells that expressed CD133 ranged from 88% to 98%.
G-CSF stem cell mobilization, collection, and isolation
Healthy subjects were given G-CSF (10 μg/kg) (Filgrastim, Amgen Thousand Oaks, CA) subcutaneously daily for 5 days. A mobilized PBSC concentrate was collected by leukapheresis (CS3000, Baxter Healthcare Corp) on the fifth day and cryopreserved in 5% DMSO and 6% pentastarch using a controlled rate freezer and stored in liquid nitrogen. The PBSC concentrate was thawed and CD34+ cells were isolated by immunoaffinity chromatography with CD34 monoclonal antibody and magnetic beads (Isolex, Baxter Healthcare). The proportion of isolated cells that expressed CD34 ranged from 87% to 98%.
Non-mobilized PBMC collection and sample preparation
A non-mobilized PBMC concentrate was collected from 7 healthy subjects by apheresis (CS3000) at the Department of Transfusion Medicine (DTM), Clinical Center (CC), National Institutes of Health (NIH). All subjects signed an informed consent approved by the NIH. Mononuclear leukocytes were separated from contaminating granulocytes and red blood cells by Ficoll gradient separation, cryopreserved and stored in liquid nitrogen. T cells, B cells, NK cells and monocytes were isolated by positive selection by using anti-CD3, anti-CD19, anti-CD56 and anti-CD14 magnetic beads, respectively (AutoMACS, Miltenyi Biotec) (purity ≥ 90%).
RNA preparation, amplification and labeling
Total RNA was isolated from each sample by using TRIZOL reagent (Invitrogen, Carlsbad, CA).
cDNA expression array
Total RNA (3 μg) was amplified from 0.5 × 106 to 107 cells into anti-sense RNA (aRNA), also, total RNA from PBMCs pooled from six normal donors was extracted and amplified into aRNA to serve as the constant reference  Test and reference RNAs were labeled with Cy5 (red) and Cy3 (green) dyes, respectively, and co-hybridized to the custom-made 17.5 K cDNA (UniGene cluster) microarrays which were printed in the Immunogenetics Section of DTM with a configuration of 32 × 24 × 23 . Clones used for printing included a combination of the Research Genetics RG_HsKG_031901 8 k clone set and 9,000 clones selected from the RG_Hs_seq_ver_070700 40 k clone set. The 17,500 spots included 12,072 uniquely-named genes, 875 duplicated genes and about 4,000 expression sequence tags. The complete list of genes included in the Hs-CCDTV-17.5k-1px printing is available at the web site http://nciarray.nci.nih.gov/gal_files/Hs-CCDTM17.5k-2px.gal.
A miRNA probe set was designed using mature antisense miRNA sequences (Sanger data base, version 8.1) consisting of 736 human, mouse, rat and virus plus two control probes. The probes were 5' amine modified and printed in duplicate in the Immunogenetics Section of the DTM on CodeLink activated slides (General Electric, GE Health, NJ, USA) via covalent bonding.Small RNA was enriched from 10 ug total RNA by flashPAGE (Pre-cast Gel, Type A) (Ambion, Austin, TX, USA) and purified using flashPAGE reaction clean-up kit (Ambion, Austin, TX, USA) according to manufacture's instruction. The same procedures were applied to obtain small RNA from the Epstein-Barr virus (EBV)-transformed lymphoblastoid cell lines that was used as the reference for the miRNA expression array assay. Fragmented small RNA were 3'-end tailed with amine-modified nucleotides and chemically coupled to CyDye fluors (Amersham Biosciences, piscatway, NJ, USA), the test sample with Cy5 and the reference with Cy3, using the mirVana miRNA Labeling Kit (Ambion) following the manufacturer recommended protocol. After labeling, the samples and the reference were co-hybridized to the miRNA array at room temperature over night. Both the processed cDNA and the miRNA array slides were scanned by GenePix scanner Pro 4.0 (Axon, Sunnyvale, CA, USA).
Data and statistical analyses
The raw microarray data set was filtered according to a standard procedure to exclude spots with minimum intensity that was arbitrarily set to an intensity parameter of ≥ 300 for cDNA expression data and ≥ 100 for the miRNA microarray data in both fluorescence channels. If the fluorescence intensity of one channel was below the cut-off while the other was above, the lower channel intensity was overridden. Spots with diameters < 25 μm for cDNA expression array and < 10 μm for miRNA microarry and flagged spots were also excluded from the analyses. Then, the filtered data were normalized using Lowess Smoother and retrieved by the BRB ArrayTool http://linus.nci.nih.gov/BRB-ArrayTools.html developed at the National Cancer Institute (NCI), Biometric Research Branch, Division of Cancer Treatment and Diagnosis. Hierarchical cluster analysis and TreeView software  were used for visualization . All of the predictions of miRNA gene targets were made using BRB ArrayTool microRNA targets http://linus.nci.nih.gov/BRB-ArrayTools.html developed at the NCI, Biometric Research Branch, Division of Cancer Treatment and Diagnosis.
Peripheral blood leukocytes and hematopoietic progenitor cells
PBMC concentrates were collected by apheresis from 7 healthy subjects. B cells, T cells, NK cells, and monocytes were isolated from each PBMC concentrate. 92% to 98% of the isolated B cells expressed CD21, 95% to 98% of T cells expressed CD3, 90% to 97% of NK cells expressed CD56 and 92% to 98% of monocytes expressed CD14. Mobilized peripheral blood HSCs were collected from 13 healthy subjects: 5 were given G-CSF and their HSCs isolated with anti-CD34 while 4 were given AMD3100 alone and 4 were given AMD3100 plus G-CSF and their HSCs isolated with anti-CD133. In the four donors given AMD3100 plus G-CSF the concentration of circulating CD34+ cells increased from 62 ± 45 × 106/L prior to the administration of AMD3100 to 215 ± 117 × 106/L twelve hours after AMD3100 was given, suggesting that AMD3100 was responsible for mobilizing a substantial portion of the circulating CD34+ cells. In the four donors given AMD3100 the CD34+ cell counts increased from a baseline level of 3 ± 4 × 106/L to 23 ± 4 × 106/L 6 hours after the administration of AMD3100.
Comparison of miRNA expression among hematopoietic progenitor cells and peripheral blood leukocytes
The make-up of the miRNAs that separated HSCs and PBLs differed markedly. Eight signature miRNAs demonstrated increased expression and 3 miRNAs decreased expression in HSCs compared to PBLs (Figure 1B). The 8 signature HSC miRNAs whose expression was increased included miR-19a, -19b, -20a, and 20b, which are part of the polycistronic cancer-associated miR-17-92 cluster. The 3 signature miRNAs whose expression was greatest in the PBL samples were miR-142-3p, miR-21, and miR-142-5p. Both probes for miR-20b were up-regulated in HSCs and both for miR-142-3p were up-regulated in PBLs.
MicroRNAs (miRs) whose expression differed among 13 hematopoietic stem cell
miRs whose expression was
increased in HSCs
miRs whose expression
was increased in PBLs
Cancer-associated microRNAs (miRNAs) whose expression was up- and down-regulated in hematopoietic stem cells (HSCs)
Fold-increase in HSCs
4 × 10-7
1.3 × 10-6
Fold-increase in HSCs
2.9 × 10-05
1.3 × 10-06
Fold-decrease in HSCs
9.93 × 10-4
Among the 148 miRNAs 47 were differentially expressed between AMD3100-mobilized CD133+ cells and the G-CSF-mobilized CD34+ cells (t-tests, p < 0.005). The expression of 17 was increased in the AMD3100 group and 30 were increased in the G-CSF group (data not shown).
The expression of 4 miRNAs were markedly increased in PBL: miR-142-3p, miR-218, miR-21, and miR-379. In addition to these 4 miRNAs, expression of miR-16 which belongs to the leukemia associated cluster miR-15a-16 was also increased.
MicoRNAs (miRNAs) characteristic of each type of peripheral blood leukocyte*
cDNA expression profiling
Genes differentially expressed between hematopoietic stem cells (HSCs) and peripheral blood leukocytes (PBLs)
Expression Increased in HSCs
Expression Increased in PBLs
GATA-binding protein 2
Caspase recruitment domain protein 14
Lymphotoxin-Beta receptor precursor = Tumor necrosis factor receptor 2 related protein = Tumor necrosis factor C receptor
CRF-BP = corticotropin-releasing factor binding protein
TDAG8 = putative G protein-coupled receptor induced during activation-induced apoptosis of T cells = G protein-coupled receptor 65
Four and a half LIM domains 1
CD16 = Fcgamma receptor IIIa
V-ets erythroblastosis virus E26 oncogene homolog (avian)
Integrin, alpha M (complement component 3 receptor 3 subunit)
Natriuretic peptide receptor C/guanylate cyclase C (atrionatriuretic peptide receptor C)
N-sulfoglucosamine sulfohydrolase (sulfamidase)
Schwannomin interacting protein 1
Integrin, beta 7
Methionine sulfoxide reductase B3
V-myb myeloblastosis viral oncogene homolog (avian)
Arachidonate 5-lipoxygenase-activating protein
DEP domain containing 6
CD48 = BLAST-1
Ependymin related protein 1 (zebrafish)
Interleukin 10 receptor, alpha
Chemokine (C-X3-C motif) receptor 1
Nerve growth factor receptor (TNFRSF16) associated protein 1
Coactosin-like 1 (Dictyostelium)
Serpin peptidase inhibitor, clade G (C1 inhibitor), member 1, (angioedema, hereditary)
ADAM metallopeptidase domain 19 (meltrin beta)
Microtubule-associated protein 7
IL-2 receptor beta chain
Suppressor of cytokine signaling 2
IL2-inducible T-cell kinase
TSC22 domain family, member 1
Killer cell lectin-like receptor subfamily C, member 4
H1 histone family, member 0
RNA binding protein with multiple splicing
CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like
Epstein-Barr virus induced gene 2 (lymphocyte-specific G protein-coupled receptor)
Cell division cycle associated 7
GTPase, IMAP family member 4
POU domain, class 2, transcription factor 2
Fms-related tyrosine kinase 3
CXCR4 = CXC chemokine receptor 4
Protein kinase, cAMP-dependent, regulatory, type II, beta
Cytochrome P450, family 4, subfamily A, polypeptide 11
Tripartite motif-containing 58
Lectin, galactoside-binding, soluble, 3 (galectin 3)
Fascin homolog 1, actin-bundling protein (Strongylocentrotus purpuratus)
Sorting nexin family member 27
Chromosome 1 open reading frame 150
Tripartite motif-containing 26
Sorting nexin family member 27
V-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
Chondroitin sulfate proteoglycan 2 (versican)
WAS protein family, member 1
In this study we discovered that miRNA expressed by HSC differed from those expressed by PBLs. We also found that miRNA profiling and cDNA expression analysis are potentially useful tools for the analysis of clinical HSCs derived by different mobilization and isolation methods which may yield functionally diverse products.
Among the 13 miRNAs increased in HSCs miR-10a, -17-5p, -19a, -19b, -20b, -93, -126, -130a, and -221; have previously been found to be expressed by HSCs [33–36]. miR-126 and miR-10a have been found to be down-regulated in erythrocyte and megakaryocyte precursors [33, 36]. miR-221 has previously been shown to be important in erythropoiesis; the expression of miR-221 and -222 inhibit erythropoiesis . The expression of miR-221 has been reported to be down regulated in CD34+ cells during erythropoesis [33, 37]. The expression of miR-221 is also increased in papillary thyroid carincomas  and is involved with the pathogenesis of hepatocelluar carincoma  and prostate cancer .
Polycistronically transcribed miRNA clusters, so called onco-miR clusters, were also highly expressed by HSCs compared to PBLs. These findings are consistent with the theory that stem cells are important in cancer. The miR-17-92 cluster has been reported to be up-regulated in diffuse large B cell lymphoma (DLBCL), lung, breast, prostate, and colon cancer [41–43]. Venurini and colleagues found that the miR-17-92 cluster was up-regulated in CD34+ cells from healthy subjects and those with early-chronic phase chronic myelogenous leukemia, but was not up-regulated in CD34+ cells from subjects with CML blast crisis . In addition, 3 of 6 members of the cancer-associated miR-106-363 cluster were also up-regulated in HSCs. Elevated expression of this cluster has been found in T cell leukemia  and T cell lymphoma .
miR-21 was increased in PBLs. miR-21 has also been found to be increased in chronic lymphocytic leukemia , B cell lymphomas , breast cancer , pancreatic cancer , head and neck cancer cell lines . In addition, the expression of miR-16 was greater in PBLs, especially in monocytes, than HSCs. miR-15 and miR-16 are cancer-associated miRNA that are down-regulated in B-cell chronic lymphocyte leukemia [52, 53] and pituitary adenomas  but upregulated in acute promyelocytic leukemia . We also found that T cells were characterized by the upregulation of miR-29a and -29b and B cells by miR-29a, -29b, and -29c. These miRNA are down-regulated in aggressive B cell lymphoma .
At the transcription level we found that the expression of a number of oncogenes and genes related to transcription was greater in HSCs than in PBLs. The expression of GATA2, a transcription factor important in hematopoietic stem cell and endothelial cell differentiation [57, 58] was 137-fold greater in HSCs and that of N-myc was 97-fold greater. Computational gene target prediction http://www.targetscan.org/ indicates that GATA2 is targeted by miR-27a whose expression was 2-fold less in HSCs than PBLs (p = 0.0069).
An interesting finding of this study resides in the differences in both miRNA and gene expression found between G-CSF-mobilized CD34+ cells and AMD3100-mobilized CD133+ cells. While both miRNA expression profiling and DNA expression profiling differentiated the two different types of HSCs, these two populations were obtained using different HSC mobilization and isolation procedures. It is not certain if the differences in the two stem cell types were due to the different mobilizing agents or isolation antibodies. We suspect that both the mobilizing agents and antibodies contributed to the differences. In addition, the G-CSF-mobilized CD34+ cells underwent an additional freeze-thaw cycle. This was not expected to affect the HSCs, but we can not exclude this possibility. Further studies are needed which compare HSCs mobilized with AMD3100 alone and with G-CSF alone and with both types of stem cells isolated with the same monoclonal antibody. Since both CD34 and CD133 are being used to isolate stem cells for clinical applications, HSCs mobilized with one agent and isolated with each antibody should also be compared.
When considering new or different mobilization or isolation protocols, changes in both the quantity and quality of HSCs should be considered. The quantitation of CD34+ cells has been the gold standard for assessing the potency of HSCs for clinical therapies. When comparing HSCs mobilized with G-CSF from different subjects, different G-CSF mobilization protocols, or different HSC collection protocols, measuring CD34+ cells is a good indicator of the potency of the HSCs. However, if stem cells mobilized with G-CSF are to be compared with those mobilized with AMD3100 or AMD3100 plus G-CSF, measuring only CD34+ or CD133+ cells may not completely reflect the differences among these types of cells. Measures in addition of CD34 and CD133 are needed to more completely characterize HSCs.
Our results show that the global miRNA and cDNA expression assessment can distinguish different types of HSCs. Both types of global gene expression arrays were able to distinguish the two types of HSCs that we studied and both should be useful for potency testing of clinical HPC components. miRNA and cDNA microarray assays with several thousand probes usually require several days to complete, but it would be possible to more rapidly analyze the expression of a smaller selected group of miRNA or genes.
In conclusion, HSCs and PBLs have unique miRNA expression profiles and many cancer-associated miRNA are expressed by HSCs. miRNA and gene expression microarrays maybe useful for assessing differences in HSCs.
We thank the Staff of the Dowling Clinic, DTM, CC, NIH for collecting the cells and the staff of the Cell Processing Laboratory, DTM, CC, NIH for isolating the CD34+ and CD133+ cells. The study was funded by the NIH, Bethesda, Maryland, USA.
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