- Open Access
Ganoderma lucidum polysaccharide extract inhibits hepatocellular carcinoma growth by downregulating regulatory T cells accumulation and function by inducing microRNA-125b
- Aimei Li†1, 2,
- Xuanyu Shuai†1,
- Zhijun Jia2,
- Hangyu Li3,
- Xiubin Liang5,
- Dongming Su1, 4, 5Email author and
- Wanhua Guo2Email author
© Li et al.; licensee BioMed Central. 2015
- Received: 7 November 2014
- Accepted: 16 March 2015
- Published: 26 March 2015
Ganoderma lucidum polysaccharides (GLPS) have been used as traditional Chinese medicine for their properties of cancer prevention and immunomodulation. However, it is unclear whether GLPS has therapeutic effect on anti-hepatocellular carcinoma (HCC) in vivo. In this study, the effect of GLPS and their impact on the balance of regulatory T cell (Treg) and effector T cell (Teff) was measured in a model of hepatoma-bearing mice.
The effect of GLPS and their impact on the balance of regulatory T cell (Treg) and effector T cell (Teff) were measured in a model of hepatoma-bearing mice. Real-time PCR detected the levels of MicroRNAs (miRNAs) and mRNA. The effects of Tregs on Teff proliferation were determined via suppression assay. The mircroRNA-125b (miR-125b) inhibitor was used to down-regulate miR-125b expression.
GLPS significantly suppressed tumor growth in hepatoma-bearing mice associated with an increase of the ratio of Teffs to Tregs. Moreover, GLPS eliminate Treg suppression of Teff proliferation with an increase in IL-2 secretion. Addition of GLPS to treat T cells inhibited Notch1 and FoxP3 expression through increase of miR-125b expression. In hepatoma-bearing mice, miR-125b inhibitor obviously abolished the effect of GLPS on tumor growth.
This finding provides the novel evidence for GLPS on inhibition of HCC through miR-125b inhibiting Tregs accumulation and function.
- Ganoderma lucidum polysaccharides
- Hepatocellular carcinoma
- Regulatory T cell
- Effector T cell
Hepatocellular carcinoma (HCC) is one of the most lethal cancers worldwide, especially in China . Due to chronic hepatitis infection and inflammation, the efficacy of chemoembolization or systemic therapies on HCC remains limited. Many researchers have found that CD4 + CD25+ regulatory T cells (Tregs) population increased in both the peripheral blood and tumor microenvironment in HCC patients, which correlates with a poor prognosis [2,3]. Tregs play a key role in impairing the anti-tumor immune response and helping tumor cells to escape from immune surveillance . Therefore, targeting the number and function of Tregs may be a useful and effective tool for HCC therapies.
MicroRNAs (miRNAs) are small non-coding RNAs involved in modulating gene expression at the post-transcriptional level . miRNAs play critical roles in several different physiological processes, such as cell proliferation, apoptosis, development, metabolism and differentiation . Increasing amounts of evidence have demonstrated that alteration of miRNAs expression is directly implicated in the process of tumorigenesis. Some miRNAs acted as tumor suppressors and others exerted an oncogenic activity [7,8]. Among these miRNAs, miR-125b aberrant expression is involved in tumorigenesis and progression of numerous human cancers . In HCC, miR-125b is significantly downregulated and exerts tumor-suppressive function . Jia et al. showed that miR-125b expression was obviously decreased in HCC tissues and cells, which is the prediction of aggressiveness and poor prognosis of HCC .
Ganoderma lucidum, a traditional remedy, has been widely used as adjuvant of anti-tumor therapy in clinic . Polysaccharides, one of the major categories of the bioactive ingredients of ganoderma lucidum, have the multiple biological activities such as improvement of host immune function, prevention of oxidative damage, protection of liver with little toxicity [13,14]. Recently, the inhibitory effect of Ganoderma lucidum polysaccharides (GLPS) on tumor has received great attention [15,16]. GLPS could inhibit the tumor growth and improve the immune function in vitro and in vivo . The immune-modulating activities of GLPS were due to different mechanisms, such as enhancing the cytotoxic activity of NK cells, activating Dendritic cells (DCs), and promoting T helper 1 immune responses . However, the molecular mechanism of GLPS on Tregs in HCC is not clear. Therefore, in the present study, we have investigated the effect of GLPS on anti-hepatocellular carcinoma in vitro and in vivo, and explored the underlying mechanisms associated with this activity.
Animals were treated humanely, using approved procedures in accordance with the guidelines of the Institutional Animal Care and Use Committee at Nanjing University. The study was approved by the Experimental Animal Ethics Committee at Nanjing University.
Chemicals and reagents
RPMI 1640 and DMEM were obtained from GIBCO (Invitrogen Company). Fetal bovine serum (FBS) was from Hyclone (Logan, UT, USA). GLPS was purchased from Johnsun Mushroom (Hangzhou, China). PHA and MTT were purchased from Sigma Aldrich (St. Louis, MO, USA). Lipofectamine 2000 transfection reagent was obtained from Invitrogen Life Technologies (Grand Island, NY, USA). Anti-mouse CD4-fluorescein isothiocyanate (FITC) and anti-mouse CD25-phycoeritrin (PE) were obtained from eBioscience (San Diego, CA, USA). Rabbit-anti-β-catenin and rabbit anti-Notch1 were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). The Detergent Compatible (DC) Protein Assay kit was purchased from Bio-Rad Laboratories (Hercules, CA, USA). The miRNeasy Mini kit, the miScript Reverse Transcription kit and the miScript SYBR Green PCR kit were purchased from Qiagen (Hilden, Germany).
The mouse hepatoma H22 cell line (syngenic to the Kunming strain of mice) and normal hepatic cell line L-02 were obtained from Chinese Academy of Sciences (Shanghai, China). H22 cells were cultured in complete RPMI 1640, and then 0.5 × 107 cells (200 μL) were injected into the abdominal cavity of mouse. Seven days later, the intraperitoneal tumor cells were collected from the mouse with ascites tumor. L-02 cells were cultured in DMEM, supplemented with 10% FBS maintained at 37°C in a humidified incubator containing 5% CO2. Cultured cells were treated with GLPS (dissolved in PBS) in complete medium.
Kunming and BALB/c male mice were purchased from Shanghai Laboratory Animal Centre (Chinese Academy of Sciences, Shanghai, China). The HCC model of mice was performed according to a previous report . Briefly, 200 μL (0.5 × 107 cells) of H22 cells suspension was injected into the abdominal cavity of Kunming mouse. Ten days later, mice were randomly and equally divided into several groups (ten mice per group). To investigate the anti-tumor effect of GLPS, mice were divided into 5 groups: injection of PBS, 10 mg/kg GLPS, 50 mg/kg GLPS, 100 mg/kg GLPS and 200 mg/kg GLPS. To observe the role of miR-125b in anti-tumor of GLPS, mice were also divided into 4 groups: injection of negative control (5′-CAGUACUUUUGUGUAGUACAA-3′), miR-125b inhibitor (5′-UCACAAGUUAGGGUCUCAGGGA-3′), GLPS + negative control, and GLPS + miR-125b inhibitor. Cholesterol-conjugated miR-125b inhibitor and negative control oligonucleotide (NC) were purchased from RiboBio (Guangzhou, China). GLPS in 0.5 ml of PBS was administered by intraperitoneal injection (i.p.) every two days for 4 weeks. In GLPS + miR-125b inhibitor group, miR-125b inhibitor was pretreated for 24 hours and then injected with GLPS. NC and miR-214 inhibitor (10 nmol) in 0.1 ml of saline buffer was administered intratumorally every 2 days for 4 weeks. Tumor growth was assessed two times a week and volume (V) was calculated using the formula V = 1/2 × length × (width)2.
Isolation of tumor-infiltrating lymphocytes (TILs)
TILs were isolated from the tumors according to previous report . Briefly, small pieces of solid tumors tissue was digested with an enzyme cocktail containing 2% fetal bovine serum, 0.5 mg/ml collagenase A (Roche), 0.2 mg/ml hyaluronidase, type V (Sigma) and 0.02 mg/ml DNase I (Sigma) per 0.25 g of tumor tissue. The cell suspensions were filtered through a cell strainer (70 μm, Becton Dickinson, CA, USA), and then, they were washed with 2% FBS in RPMI 1640. After lysed red blood cells, the cell clumps were removed by 40%/70% Percoll gradient centrifugation and centrifuged at 400 g. The nonadherent lymphocytes were harvested and CD4+ lymphocytes were isolated by Dynabeads M-450 CD4 according to the manufacturer’s instruction. These CD4+ lymphocytes were further isolated into CD25+ and CD25- lymphocytes by Dynabeads (Dynal Biotech ASA, Oslo, Norway). CD4 + CD25+ T cells and/or CD4 + CD25- T cells were added different concentrations of GLPS, and cultured for 72 h, at 37°C and 5% CO2.
Isolation of lymphocytes from peripheral blood
EDTA-K2 anticoagulated blood samples were collected from hepatoma-bearing mice. Monocytes were isolated from the peripheral blood by Ficoll-Paque (Pharmacia, Piscataway, NJ) density centrifugation. The monocytes were resuspended in RPMI-1640 medium and plated on a 6-well plate. After 2 hours of incubation at 37°C, the nonadherent lymphocytes were harvested and subsequently cultured.
Isolation of mouse naïve T cells and in vitro T cell differentiation
Splenic CD4+ naïve T cells from wild type Kunming mice were isolated using the CD4+ T cell Isolation Kit (Miltenyi Biotec, Bergisch Gladbach, Germany) following the manufacturer’s instructions. Isolated naïve T cells were added different concentrations of GLPS, and cultured in RPMI-1640 with 10% FCS with 2 ng/ml of mouse TGF-β1, 1500 units/ml of mouse IL-2, and 100 nM of retinoic acid (iTreg polarizing condition) for 7–10 days.
Flow cytometric analysis
TILs were harvested from the tumors and the lymphocytes were isolated from peripheral blood. For intracellular staining, monoclonal antibodies to surface molecules, including Anti-CD4-FITC and anti-CD25-PE were used to stain surface markers. The percentage of CD4 + CD25- and CD4 + CD25+ T cells was computed using Cell-Quest software (Becton Dickinson).
Suppression assays were performed by seeding an equal number of CD4 + CD25− T cells and CD4 + CD25+ T cells (1 × 105/well) into 96-well plates in the presence of PHA (5 μg/ml) and cultured with or without GLPS for 72 h. After 72 h, [3H]-thymidine (Amersham Biosciences) was added (1 μCi/well) for 18 h. Next, [3H]-thymidine incorporation was measured on a β-scintillation counter. Results were expressed as mean cpm ± SE.
Lymphocyte proliferation assay
The [3H]-thymidine incorporation assay was performed according to previous report . Briefly, CD4 + CD25− TILs (1 × 105 /well) were seeded into 96-well plate in the presence of PHA and cultured with or without GLPS. After 72 h, each well is pulsed with 1 μCi [3H]-thymidine for 18 h. Cells were harvested, and [3H]-incorporation measured using a β-scintillation counter. Results were expressed as the mean cell proliferation in counts per minute (cpm) ± standard error (SE).
Oligonucleotides and Cell Transfection
Jurkat T cells were seeded in 6-well or 24-well plates and transfected using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. For the knockdown of miR-125b, anti-miR-125b or a negative-control anti-miRNA (anti-NC) was used at the concentration of 100 nM. The cells were harvested 24 h after the transfection.
Quantitative real-time PCR (Q-PCR) analysis
Mature miRNAs were isolated and purified using Trizol reagent (Invitrogen, USA), according to manufacturer’s protocol. The levels of miRNAs (miR-126, miR-155, miR-146a, miR-224, miR-150 and miR-125b) were quantified by using a TaqMan PCR kit (Applied Biosystems, Foster City, CA, USA). Commercially available Taqman primers and probes, including 2 unlabeled PCR primers and 1 FAMTM dye-labeled TaqMan MGB probe were used for all the targets. Real-time PCR was performed using LighteCycler480 II Sequence Detection System (Roche, Basel, Switzerland). All reactions, including no-template controls, were performed in triplicate. After the reaction, the CT values were determined using fixed threshold settings. In order to calculate the differences of expression level for each target among samples, the 2-ΔΔCT method for relative quantitation was used. All data were analyzed using U6 small nuclear RNA as an internal normalized reference.
The mRNA expression of North1 and FoxP3 was performed using SYBR GREEN PCR Master Mix (Applied Biosystems). The specific primers were as follows: North1, 5′- CCGGTGAGACCTGCCTGAAT-3′ (forward) and 5′- GCACTTGTACTCCGTC AGCG -3′ (reverse); FoxP3, 5′-ACTGACCAAGGCTTCATCTGTG-3′ (forward) and 5′–GGAACTCTGGGAATGTGCTGT-3′(reverse); GAPDH, 5′-TGAAGCAGGCA TCTGAGGG-3′ (forward) and 5′-CGAAGGTGGAAGAGTGGGAG-3′ (reverse). All data were analyzed using GAPDH gene expression as an internal standard.
Western blot analysis
Jurkat T cells were lysed with ice-cold lysis buffer containing: 50 mmol/l Tris–HCl, pH 7.4; 1% NP-40; 150 mmol/l NaCl; 1 mmol/l EDTA; 1 mmol/l phenylmethylsulfonyl fluoride; and complete proteinase inhibitor mixture (one tablet per 10 ml; Roche Molecular Biochemicals, Indianapolis, IN, USA). Protein concentration in the cell lysate was quantified using the DC protein assay kit. Following protein content determination, western blot analysis was performed.
Analysis of IL-2 was performed using an ELISA kit according to manufacturer’s protocol. Briefly, regulatory T cells and effector T cells were incubated in a 96-well plate with different concentrations of GLPS. Production of IL-2 was normalized to protein concentrations using the DC protein assay kit (Bio-Rad).
Cell viability was determined using MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assays. The cells were seeded in 96-well dishes at 1 × 104 to 2 × 104 cells per well and pretreated with or without GLPS for 24 h. Each well was supplemented with 10 μl MTT (Sigma Aldrich) and incubated for 4 h at 37°C. The medium was subsequently removed, and 150 μl DMSO (Sigma Aldrich) were added to solubilize the MTT formazan. The optical density was observed at 490 nm.
Statistical analysis was performed with statistical analysis software SPSS 13.0 software. Statistical analyses were performed using either an analysis of variance (ANOVA) or Student’s t-test. Data were expressed as mean ± standard deviation. P < 0.05 was considered to be significant.
GLPS inhibited hepatoma growth in vivo
GLPS shifts the intratumoral regulatory T cell (Treg) to effector T cell (Teff) balance
GLPS decreases Treg-mediated suppression on Teff
miR-125b was implicated in the effect of GLPS on intratumoral Tregs
To explore the possible role of miR-125b on induction and function of Tregs, we measured the miR-125b expression in naïve T cells under iTreg polarizing condition with various concentrations of the GLPS. After 96 h of treatment, the expression of miR-125b was significantly up-regulated in a dose-dependent manner (Figure 4B). When T cells were stimulated with GLPS, the levels of FoxP3 expression dose-dependently decreased (Figure 4C and D). The role of miR-125b in the effect of GLPS on Tregs was further investigated. Through depleting miR-125b in T cells using a miR-125b inhibitor, the decrease of FoxP3 expression induced by GLPS was abolished (Figure 4E), suggesting that the inhibition of Tregs by GLPS might act through increasing miR-125b expression.
It has been demonstrated that Notch1, a target of miR-125b, plays an important role in cell growth and apoptosis of HCC [24,25]. The effect of GLPS on Notch1 expression in T cells was measured. As shown in Figure 4F, GLPS treatment significantly down-regulated Notch1 expression, which was restored by the miR-125b inhibitor (Figure 4G). In addition, treatment with curcumin, a known Notch1 inhibitor, could reverse the effect of miR-125b inhibitor on FoxP3 expression in T cells exposed to GLPS (Figure 4H). These data indicate that GLPS could decrease FoxP3 levels by miR-125b down-regulation of Notch1 expression.
miR-125b plays an important role in anti-tumor effect of GLPS
The effect of GLPS on H22 and L-02 cells viability
Ganoderma lucidum polysaccharides (GLPS), the traditional Chinese medicine, are effective in tumor therapy with low toxicity . GLPS possess anti-tumor effects on many cancers through suppression of tumorigenesis, inhibition of tumor growth and metastasis, and modulation of immune cells . In this study, the mechanism of GLPS on anti-HCC in vivo and in vitro was explored. First, we demonstrated that GLPS could significantly suppresse tumor growth in hepatoma-bearing mice associated with an increase of the ratio of Teffs to Tregs. GLPS eliminated CD4 + CD25+ Treg suppression of CD4 + CD25- Teff proliferation with an increase in IL2 secretion. Second, we showed that inactivation of tumor-infiltrating Tregs could abolish the antitumor activity of GLPS. Third, we also showed that miR-125b was implicated in the effect of GLPS on intratumoral Tregs and played an important role in anti-tumor effect of GLPS. It should be noted that GLPS had no effect on the weight of hepatoma-bearing mice (data not shown) and GLPS was little cytotoxic to normal hepatic cell line L-02 (Figure 6), which showed the safety of GLPS to treat HCC.
Regulatory T cells infiltrating the tumor play an important role in tumor immune evasion and become the main obstacle for successful HCC immunotherapy . Increased the population of Tregs in both the peripheral blood and tumor has been shown to correlate with a poor prognosis in patients with HCC . As a result, targeting the number and function of Tregs has been the target for HCC therapies. We provided a direct demonstration that GLPS treatment may definitely interfere with Treg accumulation and function in vivo. After injection of GLPS for 4 weeks, we established that the percentage of intratumoral Tregs was decreased in a dose-dependent manner (Figure 2A). The addition of GLPS to the cocultures of Tregs and Teffs resulted in a loss of Treg immunosuppressive properties (Figure 3A). However, GLPS at all tested concentrations did not stimulate Teffs proliferation without Tregs. These results demonstrated that GLPS suppressed liver tumor growth in a direct way via decreasing Tregs accumulation and activation.
Previous studies showed Notch1 signaling pathway played an important role in Treg differentiation and suppressor function through regulating FoxP3 expression . Our data exhibited that GLPS treatment significantly down-regulated Notch1 expression in T cells, which indicated that Notch1 may be involved in GLPS immunomodulatory function. Further study showed that treatment with Notch1 inhibitor could reverse the effect of miR-125b inhibitor on FoxP3 expression in T cells. This suggested that Notch1 signaling was involved in GLPS-inhibited FoxP3 expression in T cells. It has been noted that TGFβ-smad pathway play a key role in the Treg and Teff balance . We found that GLPS had no effect on the levels of TGF-β and p-Smad2/3 (data not shown), which indicated that GLPS downregulated regulatory T cells accumulation and function in a TGF-β-Independent Manner.
It has been demonstrated miR-125b expression was down-regulated in HCC, which is the prediction of aggressiveness and poor prognosis of HCC . In this study, we found that miR-125b was implicated in the effect of GLPS on anti-HCC. First, miR-125b was significantly up-regulated in intratumoral Tregs from hepatoma-bearing mice injected with GLPS. Second, miR-125b expression displayed an increase in T cells treated with GLPS. Third, Notch1, a target of miR-125b, was down-regulated by GLPS. The present study, we have demonstrated that inhibition of miR-125b expression could attenuate GLPS-induced decrease of Notch1 level. Last, the effect of GLPS on suppression of tumor growth was reversed by miR-125b inhibitor. All these lines of evidence strongly suggested that GLPS exerted anti-HCC activity through up-regulation of miR-125b expression.
GLPS effectively suppressed tumor growth in hepatoma-bearing mice. The decrease of Tregs accumulation and inactivation associated with GLPS administration was due to increase of miR-125b expression, which resulted in inhibition of Notch1 signaling pathway and FoxP3 expression. Overall, these findings have revealed the molecular mechanisms of GLPS treatment with HCC.
This work was supported by Distinguished Medical Experts Programm of Jiangsu Province, China to Dongming Su, by grants from the National Natural Science Foundation of China (81171363) to Wanhua Guo as well as by grants from the National Natural Science Foundation of China (81071955) and Scientific Research from Educational Department of Liaoning Province, China (L2010634) to Hangyu Li.
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