Gal-1 regulates dendritic cells-induced Treg/Th17 balance though NF-κB/RelB-IL-27 pathway

Abstract

Background

This study aimed to investigate the mechanism of galectin (Gal)-1 of regulating Treg/Th17 in pathogenesis of acute rejection after liver transplantation in rat.

Methods

Mononuclear cells were induced to immature dendritic cells (imDCs), which were transfected with or without NF-κB/RelB. Western Blot was performed to detect the expression of NF-κB/RelB. the expression of CD11c, CD45RB, CD80 and MHC II were detected by flow cytometry. Enzyme-linked immunosorbent assay (ELISA) was employed to detect cytokines IL-27 and TGF-β. Lewis and dark agouti (DA) rats were generally anaesthetized by isoflurane inhalation to establish liver transplant models.

Results

We demonstrate that Gal-1 disturbs maturation of imDCs by downregulating NF-κB/RelB expression, and Gal-1 negatively controls CD4⁺ proliferation though IL-27 pathway.

Conclusions

In aggregate, Gal-1 promotes Treg differentiation in CD4⁺ T cells though NF-κB/RelB-IL-27 pathway. These findings suggest a new therapeutic target to mediate Treg population.

Introduction

Organ rejection which is activated by major histocompatibility complex (MHC) significantly limits the survival of transplant patients (1,2). Regulatory T cells (Tregs) maintain immune homeostasis and induce immune tolerance (3). Studies have shown that therapeutic infusion of antigen-specific Tregs prolongs graft survival, and the number and function of Tregs in the recipient were inhibited when the rejection occurred (4,5). Therefore, it is possible to prevent organ rejection by inducing immunology tolerance with antigen specific Tregs in recipients after organ transplantation.

Dendritic cells (DCs) play an indispensable role for Treg function in vivo (6). Researches show that the mature DCs, which are stimulated by special antigen, promote Treg differentiation and induce peripheral immune tolerance (7,8). These DCs may be utilized for the treatment of autoimmune diseases and transplant rejection (9). One possible mechanism of DCs is that mature DC could be induced from immature DCs (imDCs) which uptake of apoptotic cell antigens, then the secretion of TGF-β by mature DCs promotes the proliferation and activation of Treg, which results in immune tolerance (10,11). Thus, understanding the influence mechanism of DCs-Treg becomes important for transplant rejection. RelB, a member of NF-κB family, plays a key role in the development of DCs and the DCs lack of RelB gene are unable to activate T cells (12,13). However, the specific mechanisms of these DCs and NF-κB/RelB in immune balance remain controversial.

Galectin (Gal)-1 is an endogenous lectin and a member of the glycoside binding protein family. Gal-1 is involved in various biological processes including cell adhesion, apoptosis, proliferation and metastasis. Previous studies indicate that Gal-1 plays an important role in the proliferation and apoptosis of thymic and peripheral T cells (14-16). Further research shows that sera Gal-1 levels in organ transplant recipients were significantly higher than healthy controls (17). Thus, whether there is an association between Tregs and Gal-1 is worthy of attention. IL-27 is an indispensable immune cytokine which plays complex roles in CD4⁺ T cell subsets. IL-27 induces Th1 cell proliferation through STAT1 pathway while suppresses Th2/Th17 differentiation by targeting GATA3/STAT3 (18). Although IL-27 reduces the population of peripheral blood mononuclear cell (PBMC) in peripheral blood, it does benefit Treg proliferation (19). Previous study suggests that IL-27 blocks Th17 differentiation through STAT3-IL-10 pathway (20). Gal-1 pretreated DCs (DCs-Gal-1) are able to suppress DCs-induced lymphocyte proliferation and IFN-γ production through IL-27 secretion (21). However, whether Gal-1 would have an impact on Treg/Th17 differentiation in CD4⁺ T cells remains unknown. Thus, we conducted this study to validate whether Gal-1 plays a role in DCs-induced Treg/Th17 balance through NF-κB/RelB-IL-27.

Methods

Animal

Lewis and dark agouti (DA) rats were purchased from The Beijing Vital River Laboratory, and housed in a specific pathogen-free facility in micro-isolator cages. Mice weighted 220±20 g were used. This study was carried out in accordance with the recommendations of the protocol (number NMU08-092) approved by the Institutional Animal Care and Use Committee of Nanjing Medical University.

imDCs isolation and culture

The Lewis rats were sacrificed by cervical dislocation. Mononuclear cells were obtained from femur and tibia by density gradient centrifugation and cultured in RPMI 1640 media containing 10% fetal bovine serum. Granulocyte-macrophage colony-stimulating factor (GM-CSF) (Thermo Fisher, PRC2011) and IL-4 (Thermo Fisher, RRIL410) were added to the final concentration of 50 ng/mL and 25 ng/mL, respectively.

Construction of NF-κB/RelB plasmid

The corresponding primers and enzyme sites were designed based on the sequence of RelB in Genebank and amplified by PCR. The PCR products were purified and then connected to the LV5 vector. The positive clones were transformed and screened and then the plasmids were extracted. After sequencing, the results were verified for the subsequent experiments.

Flow cytometry

Rat-specific antibodies used for flow cytometry were purchased from BD Pharmingen, BioLegend and eBioscience. Acquisition was performed using a CATON (BD Bioscience) and data were analyzed using FlowJo software (TreeStar).

Western blot and ELISA

Cells were collected and lysed. The supernatant was centrifuged and quantified by BCA quantitative kit. The expression of NF-κB/RelB was detected based on the Western blot protocol.

ELISA kits were purchased from 100 BIOTECH and the samples were collected and assayed using ELISA protocol.

Liver transplant models

Cuff technique is used according to previous reports (22,23). Briefly, both donor and recipient are generally anaesthetized by isoflurane inhalation. In donor part, large median and transverse incision was performed. Ligaments around liver were cut. A 24G, 4-mm-long stent was inserted into common bile duct. Proper liver artery was ligatured and not reconstructed. Graft was prepared on the back table and cold stored in University of Wisconsin solution (UW solution). Removal of native liver in recipient was similar to graft harvest, except the treatment of some blood vessels. Then, liver graft was implanted and the operation accomplished. A dose of 500 µg recombinant Gal-1 was injected i.p. on post-operative day (POD) 0, 2, 4, 6 in Gal-1 treatment group.

Statistical analyses

RT-PCR data were analyzed using SDS v2.3 software. Survival data were analyzed using Prism 5 (Mantel-Cox). Other data were analyzed by analysis of variance (ANOVA) or Student t-test. Probability (P) values less than or equal to 0.05 were considered statistically significant.

Results

Gal-1 suppresses NF-κB/RelB expression in imDCs

Mononuclear cells were obtained by density gradient centrifugation and cultured in RPMI 1640 media containing 10% fetal bovine serum. GM-CSF and IL-4 were added to the final concentration of 50 and 25 ng/mL, respectively. Figure 1A shows the morphological changes of imDCs isolated from rats in 5 days.

Figure 1.

Gal-1 negatively regulates NF-κB/RelB expression in imDCs (n=3). Mononuclear cells were obtained and then cultured in RPMI 1640 media containing 10% fetal bovine serum. GM-CSF (50 ng/mL) and IL-4 (25 ng/mL) were added to the final concentration. (A) The morphological changes of imDCs isolated from rats in 5 days; (B) lentivirus LV5 vector atlas was constructed as indicated (left). After 48 h transfection, the Western blot results suggest that the lentivirus successfully overexpress NF-κB/RelB levels (right); (C) Gal-1 was added at the beginning of transfection and cells were incubated in 4 different conditions (imDCs, imDCs + Gal-1, imDCs + Gal-1 + LV5-NF-κB/RelB, imDCs + Gal-1 + LV5-NC) for 24 h more after transfection and then harvested for Western blot. NC, negative control; Gal, galectin; LTR, long terminal repeat; RRE, rev response element; imDCs, immature dendritic cells; GM-CSF, granulocyte-macrophage colony-stimulating factor.

We constructed lentivirus LV5 vector atlas as indicated in Figure 1B. After 48 h transfection, as shown in Figure 1B, the Western blot results suggest that the lentivirus successfully overexpress NF-κB/RelB levels. To verify our hypothesis, Gal-1 was added at the beginning of transfection and cells were incubated in 4 different conditions (imDCs, imDCs + Gal-1, imDCs + Gal-1 + LV5-NF-κB/RelB, imDCs + Gal-1 + LV5-NC) for 24 h more after transfection and then harvested for protein assay. The result in Figure 1C demonstrates that Gal-1 downregulates NF-κB/RelB expression in imDCs, while lentivirus reversed this effect.

Gal-1 negatively controls the differentiation of imDCs into mature DCs by targeting NF-κB/RelB

We next asked if Gal-1 would play a role in the differentiation of imDCs into mature DCs. CD11c, CD45RB, CD80 and MHC II are the biomarkers of mature DCs. After transfection, we incubated these cells for 24 h more and then qualified protein expression by flow cytometry. Gal-1 treatment showed attenuated CD11c, CD45RB, CD80 and MHC II expression while the transfection of LV5-NF-κB/RelB rescued it, which indicates that imDCs maturation was suppressed by Gal-1 (Figure 2A,B,C,D). We further measured functional cytokines IL-27 and TGF-β. As indicated in Figure 2E,F, up-regulated IL-27 and TGF-β were detected in Gal-1 group while LV5-NF-κB/RelB demonstrated opposite effects. Taken together, Gal-1 treatment negatively regulates NF-κB/RelB, which is necessary for imDCs maturation.

Figure 2.

Gal-1 negatively controls the differentiation of imDCs into mature DCs by targeting NF-κB/RelB (n=3). After transfection, cells were incubated in 4 conditions as indicated for 24 h more and then assayed by flow cytometry. (A) CD80; (B) CD45RB; (C) CD11c; (D) MHC II expression and population were qualified. Cytokines such as (E) IL-27 and (F) TGF-β were measured by ELISA. Values indicate mean ± SEM of these experiments. *, P<0.05; **, P<0.01. imDCs, immature dendritic cells; NC, negative control; Gal, galectin; MHC, major histocompatibility complex; DC, dendritic cell; ELISA, enzyme-linked immunosorbent assay; SEM, standard error of mean.

Gal-1 limits DCs-induced CD4⁺ T cells proliferation through IL-27 pathway

Initially, we sorted CD4⁺ T cells from rats by flow cytometry (purity ≥94%). To ask whether Gal-1 would benefit cells expansion, the ability of proliferation was qualified by carboxyfluorescein succinimidyl ester (CFSE) assay. The result in Figure 3 showed that when naïve CD4⁺ T cells co-cultured with DCs, the proliferative ability of naïve CD4⁺ T cells was remarkably improved. However, treatment of Gal-1 (1 mg/mL) weakened this effect but this effect was reversed by anti-IL-27. The results demonstrate that DCs promote CD4⁺ T cells proliferation, and Gal-1 negatively controls CD4⁺ proliferation through IL-27 pathway.

Figure 3.

Gal-1 limits DCs-induced CD4⁺ T cells proliferation through IL-27 pathway (n=3). Naïve CD4⁺ T cells from rats were sorted by flow cytometry (purity ≥94%) and then the ability of proliferation was qualified by CFSE assay. CD4⁺ T cells co-cultured with or without DCs in 4 conditions, the CFSE fluorescence intensity and proliferation rate were qualified by flow assay. Values indicate mean ± SEM of these experiments. *, P<0.05; **, P<0.01. DCs, dendritic cells; Gal, galectin; CFSE, carboxyfluorescein succinimidyl ester; SEM, standard error of mean.

Gal-1 controls the balance of DCs-induced Treg/Th17 through IL-27 pathway in CD4⁺ T cells

After treatment in 4 conditions (none, DCs, DCs + Gal-1, DCs + Gal-1 + anti-IL-27) for 6 days in the presence of GM-CSF (50 ng/mL), Th17 (IL17⁺CD4⁺) and Treg (CD25⁺FoxP3⁺) cell populations were qualified in CD4⁺ T cells by flow cytometry (Figure 4A,B), respectively. Th17 and Treg populations were increased when CD4⁺ T cells co-cultured with DCs. Treatment of Gal-1 attenuated Th17 differentiation but showed opposite effect for Treg cells, and addition of anti-IL-27 reversed this affection. Treg/Th17 ratios were further calculated in Figure 4C, which demonstrates that when co-cultured with DCs in the presence of Gal-1 (1 mg/mL), CD4⁺ T cells showed lower Th17 and higher Treg differentiation compared to control group. Addition of anti-IL-27 (1 mg/mL) eliminated the effect of Gal-1 and induced Th17 phenotype again. Cytokines such as IL-17, IL-10, TGF-β, IL-27 are necessary for Treg function. ELISA results in Figure 4D,E,F,G suggested that, in accordingly with cells differentiation, the secretion of IL-17, IL-10, TGF-β, IL-27 was obviously increased compared to control group. Treatment of Gal-1 (1 mg/mL) decreased IL-17 expression while addition of anti-IL-27 reversed this effect with attenuated IL-10, TGF-β, IL-27 secretion. To conclude, DCs induce naïve CD4⁺ T cells differentiation into Th17/Treg cells, and Gal-1 benefits Treg population through IL-27 signaling pathway.

Figure 4.

Gal-1 regulates DCs-induced Treg/Th17 balance through IL-27 pathway in CD4⁺ T cells (n=3). After treatment for 6 days in 4 conditions in the presence of GM-CSF (50 ng/mL), Th17 (IL17⁺CD4⁺) (A) and Treg (CD25⁺FoxP3⁺) (B) cell populations were qualified in CD4⁺ T cells by flow cytometry. (C) Treg/Th17 ratios were further calculated. Cytokines such as IL-17 (D), IL-10 (E), IL-27 (F) and TGF-β (G) were further measured by ELISA. Values indicate mean ± SEM of these experiments. *, P<0.05; **, P<0.01. DCs, dendritic cells; Gal, galectin; GM-CSF, granulocyte-macrophage colony-stimulating factor; Treg cell, regulatory T cell; ELISA, enzyme-linked immunosorbent assay.

Gal-1 treatment significantly improves liver function and survival in allograft models

Allograft causes high lethality compared to syngraft, thus we established rat liver transplant models to qualify the effect of Gal-1 in the treatment. Allograft or syngraft control liver transplant were performed as indicated with or without Gal-1 treatment. As shown in Figure 5A, allograft (allo) group showed reduced graft-versus-host disease (GVHD)-induced lethality compared with syngraft group. And the treatment of Gal-1 in allograft significantly improved the survival. Consistent with survival, rat receiving allograft had highest levels of alanine transaminase (ALT) and lactate dehydrogenase (LDH) (Figure 5B,C), and Gal-1 treatment rescued liver function on day 3. We further tested the expression of serum IL-17, IL-27 and IL-10 in vivo on day 3. Although TGB-β showed no difference, the results demonstrated similar results as in vitro with lower IL-17 and higher IL-27, IL-10 expression (Figure 5D,E,F).

Figure 5.

Gal-1 treatment significantly improves liver function and survival in allograft rat models (n=10). Liver transplant models were established to qualify the effect of Gal-1 in the treatment. Allograft or syngraft control liver transplant were performed as indicated with or without Gal-1 treatment. (A) Kaplan-Meier survival curves for rats receiving transplant surgery. Levels of ALT (B) and LDH (C) were measured for liver function on day 3 after surgery. IL-17 (D), IL-27 (E) and IL-10 (F) in serum were qualified by ELISA. Data shown are representative of 2 independent experiments. Values indicate mean ± SEM of these experiments. *, P<0.05. Allo, allograft; Gal, galectin; Syn, syngraft; ALT, alanine transaminase; LDH, lactate dehydrogenase; ELISA, enzyme-linked immunosorbent assay; SEM, standard error of mean.

Thus, Gal-1 increases allograft liver transplant survival with better expression and can be exploited to improve the therapy for the prevention of human GVHD.

Discussion

Moderate Treg population is necessary for immune homeostasis. Previous studies have indicated that Treg could be induced into Th17 cells in inflammatory conditions and Treg/Th17 balance is associated with many immune diseases. In this study, we confirmed that: (I) Gal-1 downregulates NF-κB/RelB expression in imDCs; (II) Gal-1 treatment negatively regulates NF-κB/RelB, which is necessary for imDCs maturation; (III) DCs promote CD4⁺ T cells proliferation, and Gal-1 negatively controls CD4⁺ proliferation through IL-27 pathway; (IV) DCs induce naïve CD4⁺ T cells differentiation into Th17/Treg cells, and Gal-1 benefits Treg population through IL-27 signaling pathway. Gal-1 promotes Treg differentiation in CD4⁺ T cells through NF-κB/RelB-IL-27 pathway. These findings suggest a new therapeutic target to mediate Treg population.

Gal-1 suppresses T cell activation by targeting T cell receptor (TCR): (I) restriction of TCR contact sites recombination; (II) blocking TCR signaling; (III) inactivation of T cells (14,24). The role of IL-27 is more complicated because previous studies suggest that IL-27 can reduce Treg population by inhibiting its differentiation (25,26). However, the recent study has shown that although IL-27 reduces T cell number in PBMC but it could promote Treg proliferation (19). Other studies also point out that the proliferation of Treg and inhibition of Th17 differentiation require IL-27 pathway (27-29). In our study, we show that Gal-1 negatively controls CD4⁺ proliferation but promotes Treg proliferation through IL-27 pathway. Furthermore, NF-κB/RelB-IL-27 pathway in Treg is important for suppressive function and Gal-1 treatment might be a new method to improve Treg function for clinical trials.

The maturation of imDCs depends on proinflammatory stimulation and transcription factor NF-κB, especially RelA (p65) and RelB (30-32). RelB knockout mice showed impaired antigen presenting cell (APC) function and cellular immunity (12,33). We show that Gal-1 treatment downregulates NF-κB/RelB expression, which might explain for the impaired imDCs maturation. Gal-1 pretreated DCs (DCs-Gal-1) also shows enhanced STAT3 phosphorylation level compared to control mature DCs. DCs-Gal-1-induced immune regulation could be attenuated by inhibition of STAT3, which results in inhibited proliferation of CD4⁺ cells (34). Interestingly, DCs with silenced NF-κB/RelB gene show the stronger ability to induce CD4⁺CD25⁺ T cell (21,35). These findings indicate that NF-κB/RelB is necessary for imDCs maturation but adverse for Treg cell induction, which might provide new insights into the area of Treg expansion. Thus, Gal-1 inhibits NF-κB/RelB activation in DCs, and DCs-secreted IL-27 induces CD4⁺ T cells to Treg cells and changes the balance of Treg/Th17 after transplantation.

In this study, we have shown that Gal-1 treatment in vitro is an easy and efficient way of increasing the population of Treg cells, which may be useful in clinical applications. In summary, we demonstrate that Gal-1 regulates NF-κB/RelB-IL-27 pathway, which plays a vital role in tTreg expansion, and focusing on this pathway might become a new starting point in Treg clinical trials.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. This study was carried out in accordance with the recommendations of the protocol (number NMU08-092) approved by the Institutional Animal Care and Use Committee of Nanjing Medical University.