ORIGINAL RESEARCH article
Sec. Immunological Tolerance and Regulation
Volume 8 - 2017 | https://doi.org/10.3389/fimmu.2017.01991
Immunosuppressive Mesenchymal Stromal Cells Derived from Human-Induced Pluripotent Stem Cells Induce Human Regulatory T Cells In Vitro and In Vivo
- 1LP2M, CNRS-UMR 7370, Faculty of Medicine, Nice, France
- 2Université Nice-Sophia Antipolis, Nice, France
- 3Service d’Hématologie Clinique, CHU de Nice, Hôpital de l’Archet, Nice, France
- 4Pôle d’Odontologie, CHU de Nice, Hôpital Saint-Roch, Nice, France
- 5Institute for Research on Cancer and Aging of Nice, CNRS-UMR 7284-INSERM U108, Centre Antoine Lacassagne, Nice, France
Despite mesenchymal stromal cells (MSCs) are considered as a promising source of cells to modulate immune functions on cells from innate and adaptive immune systems, their clinical use remains restricted (few number, limited in vitro expansion, absence of a full phenotypic characterization, few insights on their in vivo fate). Standardized MSCs derived in vitro from human-induced pluripotent stem (huIPS) cells, remediating part of these issues, are considered as well as a valuable tool for therapeutic approaches, but their functions remained to be fully characterized. We generated multipotent MSCs derived from huiPS cells (huiPS-MSCs), and focusing on their immunosuppressive activity, we showed that human T-cell activation in coculture with huiPS-MSCs was significantly reduced. We also observed the generation of functional CD4+ FoxP3+ regulatory T (Treg) cells. Further tested in vivo in a model of human T-cell expansion in immune-deficient NSG mice, huiPS-MSCs immunosuppressive activity prevented the circulation and the accumulation of activated human T cells. Intracytoplasmic labeling of cytokines produced by the recovered T cells showed reduced percentages of human-differentiated T cells producing Th1 inflammatory cytokines. By contrast, T cells producing IL-10 and FoxP3+-Treg cells, absent in non-treated animals, were detected in huiPS-MSCs treated mice. For the first time, these results highlight the immunosuppressive activity of the huiPS-MSCs on human T-cell stimulation with a concomitant generation of human Treg cells in vivo. They may favor the development of new tools and strategies based on the use of huiPS cells and their derivatives for the induction of immune tolerance.
Among the different cells potentially used in regenerative medicine, the mesenchymal stromal cells (MSCs) are viewed as an interesting source of cells, increasingly used in the treatment of various clinical contexts as well as for immunomodulation in conditions linked to auto/allo-immunity (1). These cells are self-renewing, adhere to plastic, express characteristic surface antigens and have mesodermal multilineage differentiation potential in vitro (2, 3). MSCs can be obtained from several tissues such as adult bone marrow (BM), adipose tissue and several fetal organs. Ex vivo isolated somatic MSCs have been implicated in immune-regulatory functions on cells from both the innate and adaptive immune system. Several secreted factors such as indolamine 2,3-dioxygenase (IDO), transforming growth factor beta (TGF-β), hepatocyte growth factor, and prostaglandin E2 have been shown to mediate their capacity to inhibit T-cell activation [for review, see Ref. (1, 4)]. However, cell-to-cell contact was also shown to be involved in the T cell-inhibitory effect of MSCs, for instance, through targeting cell surface ligands of the B7 super family (5, 6).
Generation of regulatory CD4+ T cells through soluble factors produced by MSCs (7) or through interaction between MSCs and monocytes was also shown to mediate immunosuppression of T-cell responses (8). Therefore, MSCs were proposed for cell therapy for treatment of autoimmune related diseases, immunological disorders and acute graft-versus-host disease (9–13), and multiple clinical studies are ongoing (14–19).
Nevertheless, a major restriction for their clinical use is due to the limited in vitro expansion of the low quantity of cells that can be collected from adult tissues. Furthermore, their full phenotypic identity in vivo remained to be established. Therefore, MSCs derived in vitro from human-induced pluripotent stem (huiPS) cells could fulfill some of the specification required to improve MSCs use in therapeutic approaches: well-defined and unlimited number of cells with reproducible functional characteristics.
Several publications reported the generation of pluripotent cell-derived MSCs through embryonic body formation, direct differentiation, or addition of mesenchymal inductors (20–23). These pluripotent cell-derived MSCs express the classical BM-MSC CD44, CD73, CD90, and CD105 markers are capable of in vitro differentiation into osteoblasts, adipocytes, and chondrocytes and display some tissue repair activity in vivo in mouse models (24). Furthermore, they present an immunosuppressive activity in vitro against T cells (25) as well as NK cells (26). The in vivo immunosuppressive activity of such cells was so far tested on murine immune cells in different models of immunological disorders such as allergic airways (27), experimental autoimmune encephalomyelitis (25, 28), induced colitis (25), and ischemia (24).
Here, we generated huiPS-MSCs (characterized by the expression of classical markers and their multipotent property) that display in vitro an efficient immunosuppressive activity on allogeneic T-cell responses through the induction of regulatory T (Treg) cell differentiation. We further demonstrate that their infusion in humanized NSG mice [human peripheral blood mononuclear cell (PBMC) mouse] induced a decrease in the proportion of human CD4+ and CD8+ T cells expanding within the mice, along with a switch from a Th1 cytokine profile toward a Treg signature. Our data highlight the promising therapeutic potential of huiPS-MSCs in immune-mediated diseases.
Materials and Methods
All the culture products were provided by ThermoFisher (France) unless mentioned. In this study, the induced pluripotent stem (huiPS) cells were provided by Dr. I. Petit (INSERM U976, Paris) obtained from the reprogramming of human adult fibroblasts (29) or were produced in the laboratory (30). These cells were grown into homogeneous colonies on feeder mouse embryonic fibroblasts (MEFs) treated with mitomycin C (Sigma, France). The culture medium of huiPS cells consisted in 85% DMEM/F12, 15% knockout serum replacement, l-glutamine 100 mM, β-mercaptoethanol 0.1 mM, and bFGF 10 ng/ml (Invitrogen or Peprotech, France). The huiPS cells were passaged one to two times per week by splitting colonies in dissociation buffer (DMEM containing Collagenase type IV 2 mg/ml) without detaching the feeder MEF.
Human iPS-derived mesenchymal stromal cells (huiPS-MSC) were obtained by spontaneous differentiation of huIPS cells. For this, huiPS cells were maintained in huiPS medium without bFGF until the huiPS colonies overgrew. Without passaging them, the differentiating cells were maintained for the next 4–6 days in an “MSC” culture medium containing 30% DMEM, 30% F12, 10% serum FcII (Hyclone, ThermoFisher, France), NEAA 10 mM, Na pyruvate 1 mM, penicillin (1 U/ml)/streptomycin (1 μg/ml), glutamine 1 mM, β-mercaptoethanol 100 μM, ascorbic acid 50 μg/ml (Sigma-Aldrich, France), and huEGF 10 ng/ml. The differentiating cells were then dissociated in PBS 0.05% trypsin–EDTA, and put back in culture in the “MSC” medium. Only few cells collected (<10%) were able to survive and grow (medium was changed 1 or 2 days later to removed dead cells and floating cells). The “MSC” medium was then changed every 3–4 days. Ten to fifteen days later, the cells were passaged (passage 1) and analyzed for the expression of MSC markers (usually 80–90% of cells with MSC phenotype are recovered). These huIPS-MSCs were then maintained in culture and passaged one to two times per week in “MSC” medium. Although the huiPS-MSCs obtained could be maintained up to passage 10, they were used before they reached passage 5.
Human PBMCs were obtained from the EFS (Etablissement Français du Sang) from healthy platelet donors. After separation on a Ficoll gradient, the cells were immediately used or frozen and stored in liquid nitrogen.
In Vitro Differentiation of huiPS-MSCs
Human-induced pluripotent stem-MSCs’ differentiation into adipocytes and chondrocytes was performed using specific differentiation media (StemProAdipocyte medium and StemProChondrogenesis medium, ThermoFisher) according to the manufacturer’s instructions. Osteoblast differentiation was performed in αMEM medium containing 5% Hyclone serum supplemented with ascorbic acid 50 μg/ml, β-glycerophosphate 110 μM, and dexamethasone 0.1 μM. After 14–21 days of culture and fixation, the cells were treated with either Alcian Blue 1% for coloration of chondrocyte matrix, Alizarin Red 2% for osteoblast-derived matrix or Red Oil for presence of lipid droplets as a marker of adipocytes.
Flow Cytometry Analysis
The cells were labeled for expression of surface markers with fluorescent antibodies in PBS plus 1% FCS and 2 mM EDTA for 30 min at 4°C and were analyzed on a FACS Canto II with the Diva (Becton-Dickinson, France) or the FlowJo (FlowJo, LLC) softwares. The anti-CD90 FITC (clone 5E10), anti-CD105 PeCy7 (clone SN6), and anti-CD3 eFluor450 (clone UCHT1) antibodies were provided by eBioscience SA (France). The anti-CD73 APC (clone AD2), anti-CD4 PeCy7 (clone SK3), and anti-CD8 PerCP-Cy5 (clone SK1) antibodies were provided by Becton-Dickinson.
For intracytoplasmic staining of cytokine expression, human T cells were stimulated for 4 h with Ionomycin (10 μg/ml) and PMA (1 μg/ml) in the presence of Brefeldin A (10 μg/ml) [as already described (31)]. T cells were labeled with the anti-CD4 PeCy7 and anti-CD8 PerCP-Cy5 antibodies, fixed and permeabilized with the Fix/Perm buffer (eBiosciences). They were incubated with antibodies specific (from eBioscience) for the following cytokines: IFNγ (clone 45.B3), TNFα (clone MAb11), and IL-10 (clone Jes3-9D7). A nuclear labeling of fixed and permeabilized human CD4+ and CD8+ T cells was performed to detect the expression of the FoxP3 transcription factor (APC, clone 259D/C7, Becton-Dickinson). In some experiment, the following antibodies were used CD3 BV510, CD4 PerCP-Cy5, CD127 PeCy7, Neuropilin (Nrp1) BB 515, Helios AF 488, and FoxP3 APC (all from Becton-Dickinson).
Mixed Lymphocyte Reaction (MLR)
Responder PBMC labeled with 0.4 μM CFSE (ThermoFisher) was stimulated by allogeneic manner in MLR with irradiated (40 Gy) PBMCs from two different donors labeled with 0.4 μM APC-Cell Tracer (eBioscience) and cocultured with or without irradiated (60 Gy) huiPS-MSCs (ratio 1 huiPS-MSC for 10 immune cells) in a u-bottom 96 well plates for 5 days. The cells then were collected and labeled with the anti-CD4 PeCy7 and anti-CD8 PerCP antibodies and then analyzed by flow cytometry. We excluded stimulator cells stained with the APC-Cell Tracer. The proliferation of CD4+ and CD8+ responder T cells was measured by the dilution of the CFSE marker. In some experiments, the PBMCs were put in the insert of a Transwell culture system (Nunc, 0.45 μm pores), the huiPS-MSC being put in the lower part. A rat anti-human blocking IL-10 antibody (clone JES3-19F1, Becton-Dickinson) and an isotype rat control were used (10 μg/ml) to inhibit the potential role of IL-10 in the immunosuppression.
The In Vivo Model of Human T Cell Expansion in NSG Mice
NOD/SCID/IL2Rγ KO (NSG) mice were purchased from Charles River Laboratory. Animals were maintained in accordance with the general guidelines of the institute. They were injected ip with 10 × 106 human PBMC and were treated with or without 1 × 106 huiPS-MSCs by ip injection once a week for 3 weeks. In some experiments, mice received only the huiPS-MSCs. Mice were sacrificed between weeks 5 and 7 after PBMC injection. Peritoneal fluid, blood, and spleen were collected for flow cytometry analysis. Approval for the use of mice in this study was obtained from our local Institutional Ethic Committee for Laboratory Animals (CIEPAL-Azur, NCE/2013-102).
We determined by ELISA the concentrations of human IL-1a, IL-6, IL-8, IL-2, and IFNγ (Development kit, Peprotech) in MLR culture media according to the manufacturer’s instructions.
RNA Extraction and Quantitative Real-time PCR
Total RNA was extracted and reverse transcribed (SuperScript II Reverse Transcriptase, Invitrogen), and real-time RT-PCR was performed on an StepOnePlus Fast real-time PCR system (SybR Green, Applied Biosystems) on triplicates as described. Results were normalized to the different housekeeping genes (ACTIN, GAPDH, and UBIQUITIN) on the same plate. Differences in gene expression were calculated using the 2−ΔΔCt method.
Results are presented as mean ± SD. The level of statistical significance was determined by the unpaired two-sample Student’s t-test. p Values <0.05 were considered statistically significant.
Characterization of huiPS-MSCs: Phenotype and In Vitro Multipotency
Because previous differentiation protocols of MSCs from pluripotent cells involve many steps ranging from embryonic body formation to cell sorting or both (20, 22, 32–36), we set up a simple two-step protocol that would generate rapidly mesodermal-derived cells (Figure 1A). Cultured human iPS cells were kept in absence of bFGF for 7 days, followed by a change for an ectodermal/mesodermal medium (37) for the next 2 weeks. Eighty to ninety percent (at passage 1) and 100% (at passage 2) of the recovered cells (Figure 1B) express surface antigens (Ags) known to be expressed by tissue-derived MSCs. They were positive for CD44, CD73, CD90, CD105, and HLA-ABC Ags but negative for the endothelial CD31 marker, the hematopoietic and immune related CD34, CD45 markers, HLA-DR antigens, and CD80 and CD86 co-stimulatory molecules (Figure 1B; Figure S1 in Supplementary Material). Three different human iPS cell lines, prepared from different donors and from different tissues [skin fibroblast (29, 38) or myoblasts (30)] behaved identically, confirming that this protocol is applicable for multiple human iPS cells.
Figure 1. Characterization of human-induced pluripotent stem (huiPS) cells differentiated in huiPS-mesenchymal stromal cells (MSCs). (A) The picture in the upper panel shows undifferentiated huiPS cells in culture on mouse embryonic fibroblast feeder cells (bar = 200 μm); the two bottom pictures represent huiPS-MSCs showing typical shapes and obtained after two passages in differentiated medium (bars = 200 and 100 μm, respectively). (B) Flow cytometry analysis of huiPS-MSCs showing the typical expression of CD90, CD73, CD105, and CD44 and the absence of expression of CD31 and CD34. (C) Multipotency of huiPS-MSCs was assayed after culture in specific medium for 14 days for the adipocyte and chondrogenic differentiation or for 21 days for the osteogenic differentiation. Specific extracellular matrix components were colored with Alzarin Red (for osteoblast) and Alcian Blue for chondrocytes, while adipocytes were detected with Oil Red coloration of lipid droplets. (D) Histogram bars representing the level of IL-1α, IL-6, and IL-8 cytokines produced in vitro by huiPS-MSCs, as detected by ELISA, after 1–5 days in culture (mean ± SD of values from three independent experiments expressed as picograms per milliliter).
In addition, the cells recovered and further kept in culture were capable of differentiation into the classical mesenchymal-derived cells (osteoblasts, chondrocytes, and adipocytes) (Figure 1C) when cultured with appropriate differentiation media, suggesting that the huiPS-MSC population contained multipotent cells and correspond to bona fide MSCs. Finally, the huiPS-MSCs we have generated secreted high and sustained amount of IL-6 and IL-8 cytokine/chemokine but low amount IL-1α (as tested by ELISA) (Figure 1D), a cytokine profile shared by tissue-derived MSCs and associated with their role in tissue repair (39, 40). Altogether, these results highlight that the huiPS-MSCs generated with our protocol shared strong similarities with in vitro maintained MSCs derived from adult tissues (2, 3).
In Vitro Immunosuppressive Activity of huIPS-MSCs on Activated T Lymphocytes
Besides their multipotent characteristics, tissue MSCs display in vitro immunosuppressive activities. To test the immunosuppressive properties of the huiPS-MSCs, we analyzed their action on the proliferation of human T lymphocytes stimulated in an allogeneic manner (Figure 2A). The stimulation of PBMCs in MLR with allogeneic antigen-presenting cells (PBMC from a secondary donor—in here named alloAPC) resulted in CD4+ and CD8+ T-cell proliferation, which was significantly reduced in coculture with huiPS-MSCs. We further observed a significant reduction in the % of CD25-expressing CD4+ and CD8+ T cells, indicating a diminished proportion of activated T cells in coculture with huiPS-MSCs (Figure 2B). Another activation marker (CD69) was on the contrary expressed on a higher % of CD4+ and CD8+ T cells (Figure 2B). Known to be an early activation marker, its maintained expression might indicate that the immunosuppression required to be effective the early activation of the T cells. It is also expressed on memory T cells, which would suggest that the remaining T cells in the coculture might acquire such a “memory” phenotype. We also analyzed by RT-qPCR the relative expression of mRNAs coding for cytokines as well as some surface receptors involved in such immune reactivities (Figure S2 in Supplementary Material). As expected, gene expression signature of activated T cell was clearly reversed upon exposure with huiPS-MSCs. Indeed, compared with the RNA expression by huiPS-MSCs alone or in coculture with unactivated T cells, the relative expressions of activated T-cell cytokines (IL-2, IFNγ, TNFα, and TNFβ) were reduced in the MLRs in the presence of huiPS-MSCs (Figure S2A in Supplementary Material). Measured by ELISA (Figure 2C), the IL-2 and IFNγ production was indeed reduced in the cocultures with huiPS-MSCs confirming at the protein level the lower activation of T lymphocytes observed in such conditions. Furthermore, RNA expression of other genes coding for cytokines were affected (Figure S2A in Supplementary Material): we observed an increased expression of inflammatory IL-1α and IL-1β, IL-6 (cytokines that were shown to sustain the immunosuppressive activity of MSCs), as well as TGF-β and LIF known for their immunosuppressive functions. The mRNA coding for the cytokine IL-10 was also overexpressed. However, its immunosuppressive function appeared to be not involved in the T-cell immunosuppression. Indeed, using anti-IL-10-blocking antibodies during the initial MLR in the presence of huiPS-MSCs did not affect the inhibition of the T-cell proliferation (Figure S3A in Supplementary Material). Tested in transwell assay, we observed that the level of inhibition of the CD4+ T-cell proliferation was partially reduced (Figure S3B in Supplementary Material). This indicated that both cellular contacts between activated T cells and huiPS-MSCs, and soluble factors were involved in the immunosuppressive function of the huiPS-MSCs. On the contrary, the proliferation of the CD8+ T-cell population appeared to be less inhibited in the transwell assay, suggesting that their immunosuppression required a direct contact between T cells and huiPS-MSCs. The relative RNA expression of surface molecules involved in the T-cell activation and their polarization into effector cells such as OX40 and its ligand (OX40L), as well as CD47 were diminished, while on the contrary, those of LAG3 and CTLA4, potentially involved in immunosuppressive functions were increased in the MLR in the presence of huiPS-MSCs (Figure S2B in Supplementary Material). Altogether, these observations might indicate a change in the polarization of the T-cell populations activated in the presence of huiPS-MSCs.
Figure 2. In vitro immunosuppressive activity of human-induced pluripotent stem (huiPS)-mesenchymal stromal cells (MSCs) on human T lymphocytes. (A) In vitro immunosuppressive activity of huiPS-MSCs on human CFSE-labeled peripheral blood mononuclear cell (PBMC) stimulated for 5 days with irradiated allogenic PBMC (as alloAPC) in the presence or absence of huiPS-MSCs. The percentage of proliferating CD4+ and CD8+ T cells (assessed by CFSE dilution) was then determined by flow cytometry. The graph represents the mean ± SD of values from five independent experiments, with the corresponding p values. (B) The proportion of CD4+ (left panel) and CD8+ (right panel) T cells expressing CD25 and CD69 was determined by flow cytometry. The histogram represents the mean % ± SD with the corresponding p values calculated from three independent experiments. (C) Analysis by ELISA of IL-2 and IFNγ cytokines (pg/ml) at day 4 in cultures of allogenic stimulated PBMC in the presence or absence of huiPS-MSCs. The graphs represent the mean ± SD of values from three independent experiments, with the corresponding p values.
huiPS-MSCs Induced a Switch in T Cell Polarization
Using intracytoplasmic cytokine detection by flow cytometry in activated T lymphocytes, we observed a dramatic reduction in the proportion of CD4+ T lymphocytes producing IFNγ and TNFα corresponding to Th1 cells in MLR with huiPS-MSCs (Figure 3A). Furthermore, we detected the presence of CD4+ Treg cells among the T populations recovered from the cocultures. As shown in Figure 3B, the MLR without huiPS-MSCs generated only a small amount of FoxP3+ CD4+ T cells, while in the presence of huiPS-MSCs this percentage strongly increased up to 16%. FoxP3 being susceptible to reflect human T-cell activation, we confirmed the presence of CD4+ Treg cells since we observed an increased detection of a population of CD4+ T cells expressing a high level of the CD25 and a low level of CD127 markers (Figure 3C). This CD4+ CD25hi CD127lo T-cell population further contained a higher proportion of FoxP3 cells (Figure 3C). To better define the phenotypic characteristic of the Treg cell population induced in the presence of huiPS-MSCs, we showed that the neuropilin1 (Nrp1) surface marker was not particularly expressed by such Treg cells and that the Ikaros family member Helios was clearly highly expressed in the whole CD4+ T cells population (reflecting a global activation) (Figure S4 in Supplementary Material). Finally, this CD4+ T-cell population recovered from the cultures in the presence of the huiPS-MSCs was then assayed in a secondary MLR. As shown in Figure 3D, this CD4+ T-cell population containing Treg cells was very efficient to inhibit CD4+ T-cell proliferation. Indeed, we observed 50 and 70% inhibition of cell proliferation when the ratios of Treg cells over CD4+ T cells were 1 for 3 and 1 for 2, respectively. We thus demonstrated that the FoxP3+ CD4+ T cells generated during the coculture with the huiPS-MSCs are immunosuppressive CD4+ Treg cells.
Figure 3. Switch in T-cell effector function induced by human-induced pluripotent stem (huiPS)-mesenchymal stromal cells (MSCs). (A). Analysis by flow cytometry of intracytoplasmic production of Th1 cytokines (IFNγ and TNFα) performed on CD4+ T lymphocytes after allogenic stimulation without (no) or with huiPS-MSCs cocultures. The histogram represents the % of CD4+ T cells expressing INFγ (mean % ± SD and p value calculated from three independent experiments). (B) Detection of CD4+ FoxP3+ regulatory T (Treg) cells after mixed lymphocyte reaction (MLR). The dot plots show the % of FoxP3-expressing CD4+ T cells determined by flow cytometry after specific intranuclear staining of FoxP3 performed on CD4+ T lymphocytes after allogenic stimulation without (no) or with huiPS-MSCs cocultures. The histogram represents the mean % ± SD with the corresponding p values calculated from three independent experiments. (C) The proportion of CD4+ T cells expressing high level of CD25 (CD25hi) and no or low level of CD127 (CD127lo) was determined by flow cytometry. Further gated on this population, the level of FoxP3 expression was analyzed. The histogram represents the mean % ± SD with the corresponding p values calculated from two independent experiments. (D) Treg cells obtained in the MLR in the presence of huiPS-MSCs are immunosuppressive in vitro. Mix lymphocyte reactions (with different cell ratios) were realized between activated CFSE-labeled CD4+ T cells and the CD4+ Treg cell containing population obtained from previous coculture of T cells with huiPS-MSCs. The left panel shows a representative graph indicating the level of CFSE dilution (i.e., proliferating CD4+ responding T cells) at three different ratios after 4 days in culture and analyzed by flow cytometry. The right panel displays the proportion of proliferating CD4+ T cells expressed in percentage of proliferation of CD4+ T cells in the absence of the Treg cell containing population. The histogram represents the mean % ± SD with the corresponding p values between ratio 0/1 and either ratio 1/3 or 1/2 calculated from three independent experiments.
Altogether, these results highlight the immunosuppressive activity in vitro of the huiPS-MSCs on T-cell stimulation that induces a switch in T-cell cytokine polarization and the generation of Treg cells.
In Vivo Suppressive Activity of huiPS-MSCs
We further tested the immunosuppressive activity of huiPS-MSCs in a model of human T-cell expansion in immune-deficient NSG mice (41). First, we determined whether ip-injected huiPS-MSCs could be detected in different compartments in NSG mice. HLA-ABC+ huiPS-MSCs were labeled with CFSE and injected ip in NSG mice. Despite a lower level of expression of CD73 on recovered cells, we showed that CFSE+ HLA-ABC+ huiPS-MSCs could be detected up to 7 days after injection not only within the peritoneal cavity but also among the circulating cells and splenocytes (Figures 4A,B). This indicated that the injected huiPS-MSCs remained viable for at least 7 days within these mice and were able to circulate at least up to the spleen.
Figure 4. Human-induced pluripotent stem (huiPS)-mesenchymal stromal cells (MSCs) injected in NSG mice remained detectable for 7 days. (A) CFSE-labeled huiPS-MSCs were injected ip (1 × 106 cells) and were detected within NSG mouse peritoneal fluid and among splenocytes through their CFSE label and their expression of HLA-ABC and CD73 by flow cytometry (% of positive cells are given). Days 2 and 7 after injection are represented. Note that CD73 expression progressively decreased in vivo. (B) CFSE+ HLA-ABC+ huiPS-MSCs were detected up to 7 days after injection in the peritoneal fluid, blood, and the spleen of NSG mice. The graph represents the percentage of huiPS-MSCs among all cells recovered from the different mouse tissues at different days after ip injection. The graph displays the mean % ± SD of triplicate determinations from two mice sacrificed at the indicated days and is representative of two independent experiments.
In a second step, we tested their impact in vivo on the expansion of human T cells. NSG mice were injected with human PBMC, were then treated or not with three infusions of huiPS-MSCs (through ip injection at 1-week intervals), and were sacrificed between weeks 5 and 7. After sacrifice, cells collected from the peritoneal cavity, those circulating in the blood and those present in the spleen were analyzed by FACS analysis (not shown and Figure 5) on the basis of expression of the human CD45 Ag. Within the peritoneal cavity, human CD45+ cells represented about 65% of total cells recovered from control or huiPS-MSCs-treated mice; more than 95% of them were CD3+ T cells (not shown). This indicated that among the injected PBMC, T cells were the main human cell population able to expand and colonize the mice. Accordingly, we observed in the blood and spleen that more than 90% of human CD45+ cells were CD3+ T cells with expected proportion of CD4+ and CD8+ cells, indicating a similar rate of expansion. But when mice were treated with huiPS-MSCs, the percentage of circulating human T cells was significantly reduced about 1.8-fold (Figure 5A) leading to a 1.6-fold reduced accumulation of total T cells within the spleen (Figure 5B). Interestingly, the proportion of both CD4+ and CD8+ T cells was changed, the CD8+ T cells being significantly more affected by the huiPS-MSCs treatments (Figure 5B).
Figure 5. In vivo immunosuppressive role of human-induced pluripotent stem (huiPS)-mesenchymal stromal cells (MSCs) infusion in a model of human T-cell expansion in NSG mice. NSG mice injected with human peripheral blood mononuclear cell (PBMC) were treated or not (no) with three infusions of 1 × 106 huiPS-MSCs (at 1-week intervals), and human cells were analyzed by flow cytometry 5–7 weeks after PBMC injection. (A) % of Human CD45-, CD3-, CD4-, and CD8-positive-circulating cells recovered from the blood. (B) Absolute number of human CD45-, CD3-, CD4-, and CD8-positive cells recovered from spleens. Six mice per group were analyzed. The graphs display the value for each mouse (squares for not injected and rounds for huiPS-MSCs-injected mice) and their mean (horizontal bar) ± SD. The p values between not injected and huiPS-MSCs-injected mice are indicated for each panel. Data are representative of three independent experiments.
Intracytoplasmic labeling of cytokines produced by the human T cells recovered from the spleen was performed. We showed that untreated mice displayed high percentages of human inflammatory IFNγ+ TNFα+ Th1 cells, while little or none produced the anti-inflammatory IL-10 cytokine (Figure 6A). By contrast, in mice treated with the huiPS-MSCs, the proportion of Th1 cells was substantially reduced, while the one of T cells producing IL-10 was increased more than sixfolds. In parallel, FoxP3+ CD3+ Treg cells were absent in non-treated animals whereas they were systematically detected in huiPS-MSCs injected mice (Figure 6B).
Figure 6. Increased proportion of regulatory T cells after human-induced pluripotent stem (huiPS)-mesenchymal stromal cells (MSCs) infusion in the NSG mouse model of human T-cell expansion. (A) The left panels display a representative intracytoplasmic labeling of human T cells recovered from spleens of peripheral blood mononuclear cell (PBMC)-humanized NSG injected (huiPS-MSCs) or not (no) with huiPS-MSCs for the detection of IFN-γ- and IL-10-producing T cells. The right panels represent the percentage of Th1 cells and IL-10-producing T cells in mice injected or not with huiPS-MSCs. The graphs display the % of positive T cells for each mouse (squares for not injected and rounds for huiPS-MSCs injected mice), the mean (horizontal bar) ± SD. The p value between not injected and huiPS-MSCs-injected mice is indicated for both panel. Six mice per group were analyzed. (B) The left panels display a representative intracytoplasmic labeling of human T cells recovered from spleens of PBMC-humanized NSG injected or not with huiPS-MSCs for the detection of FoxP3-expressing T cells. The right graphs display the % of FoxP3-positive T cells for each mouse (squares for not injected and rounds for huiPS-MSCs injected mice, n equal 6 per group), the mean (horizontal bar) ± SD. The p value between not injected and huiPS-MSCs-injected mice is indicated. Data are representative of two independent experiments.
Altogether, these data demonstrated that the huiPS-MSCs were able to limit the human T-cell expansion in vivo, along with a reduced Th1 inflammatory cytokine profile, the presence of IL-10-producing T cells and the generation of FoxP3+ Treg cells.
Mesenchymal stromal cell clinical use, through many therapeutic protocols, has proven its safety and efficacy in the treatment of various degenerative diseases and tissue injuries. Since the pioneering work by Takahashi et al. on the derivation of induced pluripotent stem cells (42, 43), tremendous progresses enables to imagine the future safe clinical applications of such cells in regenerative medicine.
In this study, huiPS cells were used to efficiently generate stromal mesenchymal cells (huiPS-MSCs) with a simple spontaneous differentiation method. As other studies evaluating the properties of MSCs derived from pluripotent cells (21), we confirmed that the cells we obtained exhibit the morphologic, phenotypic, and immunomodulatory characteristics assigned to adult tissues—or cord blood-derived MSCs (4). They fulfill the defined standards attributed to in vitro-expanded MSCs derived from BM with the lack of expression of specific hematopoietic and endothelial cell markers, and as expected, they express the MSC-identifying markers CD73, CD90, and CD105 (3). As their ex vivo counterpart, the huiPS-MSC population we generated is able to give rise, in appropriate culture conditions, to osteoblasts, chondrocytes, and adipocytes revealing similar multipotent property. Furthermore, they produced IL-6 and IL-8, cytokines known to be associated with MSC tissue repair potential (39, 40).
Among the different approaches used to differentiate pluripotent cells into MSCs, either embryonic bodies formation or the use of flow cytometry cell sorting might complicate the large-scale production of such cells for industrial or clinical applications. The protocol we set up allows to generate huiPS-MSCs in 2 weeks from confluent iPS cell cultures. This simple protocol, fast and not expensive, revealed to be efficient and reproducible. Nevertheless, the cellular and molecular mechanisms involved in the in vitro differentiation of MSCs from pluripotent stem cells in our hand and in many of the published studies remained to be characterized. Some insights were recently provided indicating that MSCs could be derived from hES cells via a trophoblast-like intermediate state (25) or increased through the inhibition of the IKK/NF-κB signaling pathway (23). Such studies provide new tools not only to generate efficiently MSCs in vitro but also for a better understanding of the in vivo origin of MSC populations.
We also analyzed in vitro some of the mechanisms of immunosuppression exhibited by the huiPS-MSCs cells we have generated. Many in vitro and in vivo studies reported the potent immune modulating functions of tissue-derived MSCs through action on different types of immune cells, activated through variable means (1, 4). Concentrating on human T cells in our study, stimulation of PBMC by MLR in coculture with the huiPS-MSCs resulted in a dramatically decreased proliferation of both CD4+ and CD8+ T lymphocytes and a concurrent decrease in IL-2 and IFNγ production, both cytokines associated with inflammatory activation of T cells.
The transcriptomic analysis we performed gave some insight into the potential mechanisms involved in the immunosuppression. While we observed a contradictory increased expression of IL-1α, IL-1β, and IL-6, considered as “inflammatory” cytokines, those were shown to be necessary sustain the immunosuppressive activity of MSCs (1) and could therefore participate to the overall immunosuppression. We also noticed a diminished expression of co-stimulatory molecules involved in the T-cell activation and in their polarization into effector cells such as OX40L (44) and CD47 (45). On the contrary, those of LAG3 (46, 47) and CTLA4 (48, 49), both described for their potent immunosuppressive functions on T cells, were increased in the MLR in the presence of huiPS-MSCs. Likewise, the higher RNA expression of IL-10, TGF-β, and LIF, well-known strong immunosuppressive cytokines (1, 50), strengthens the immunosuppressive action on T cells by the huiPS-MSCs. To be noticed, even if the level of RNA expression for PD-L1 (B7H1, CD274), one other well-known immunosuppressive molecule appeared reduced upon exposure of activated PBMCs to huiPS-MSCs (compared with activated PBMCs), the involvement of this pathway is clearly engaged (not reported in here). Altogether, our data point out the package of multiple mechanisms contributing to inhibit the T-cell immune system used by the huiPS-MSCs similarly to tissue somatic MSCs.
Finally, among the molecular pathways able to impact effector T cells, the huiPS-MSCs we have generated were able to induce in vitro the differentiation of functional CD4+ Treg cells expressing FoxP3 as well as CD25 at high level and not expressing CD127 (51), at the expense of IFNγ+ TNFα+ inflammatory T cells. Treg cells were shown to depend on TGF-β signaling for maintenance of their immunosuppressive function (52). Such mechanism may be involved in our hand as the huiPS-MSCs produced a very high amount of TGF-β (not shown). It remains to determine whether such a Treg cell population is indeed induced in vitro or simply expanded from natural Treg present within the PBMC used (53). The expression of the Neuropilin1 or the Helios markers could be used to discriminate between natural and induced Treg cells (54–57). However, this remains controversial (57–60). The population we generated did not expressed Neuropilin1, consistent with an induced phenotype. Regarding Helios expression, it was highly expressed on the Treg cells tested. But Helios has also been described to be highly expressed on induced Treg cells and is a marker of T-cell activation and proliferation (61, 62). Nevertheless, the presence of cytokines such as IL-2 (which level is inhibited but not abrogated), TGFβ, and IL-6 in the MLR we have performed with huiPS-MSCs suggest that the Treg cells obtained could be induced in vitro (63).
Interestingly, because of these different characteristics, one might consider the clinical use of huiPS-MSCs in strategies aiming at inducing immune tolerance toward other human iPS cell type derivatives. Indeed, the clinical use of autologous iPS-derived cells might be compromised by the overall genetic instability generated during the reprogramming of epigenetic defined somatic cells. Allogenic, genetically stable, iPS cell line banks could be the clinical alternative provided that the challenge of immune rejection of transplanted allogenic cells would be resolved. As discussed recently by Liu et al. (64), some proposed strategies that could be considered, involve known tolerogenic pathways through forced expression of CTLA4-ig and PD-L1 by iPS-derived cells. Because they are able to generate Treg cells and probably innately use CTLA4/CD28 as well as PD-L1/PD1 axes on T cells to block their reactivity [as does the tissue MSCs—(1, 4)], huiPS-MSCs could be included within the arsenal of tools used to promote immune tolerance as an associated cell type proposed along with the therapeutic transplanted iPS-derived cells.
To the best of our knowledge, this study is the first evaluating the huiPS-MSCs immune-regulatory properties on human T-cell responses in vivo through the potential generation of Treg cells. The model of humanized NSG mouse allows to evaluate the state of activation of human T cells recovered from different organs (peritoneal fluid, blood, and spleen) after treatment with the huiPS-MSCs. Indeed, injection of human PBMC in such immunocompromised mice led to the expansion, circulation, and accumulation (within the spleen) of human activated CD3+ T cells, other CD45+ cells (such as B lymphocytes, NK cells, or monocytes) being barely detected within the different tissues. Furthermore, NSG mice were not irradiated before human cell injections [as done in many NSG models (65–67)] to avoid possible repair mechanisms of huiPS-MSCs on irradiated tissues that could interfere with their immune suppressive action on T cells. Finally, the huiPS-MSCs were injected ip instead of iv to prevent possible pulmonary embolization known to lead to massive secretion into the blood of immune modulating factors such as TSG6 (68). This ip mode of injection did not confine the huiPS-MSCs to the peritoneal cavity since we were able to detect them over 7 days in the blood stream as well as in the spleen. These results indicate that huiPS-MSCs were able to migrate to different area, colonized as well by human activated T cells, where they might exert their immunosuppressive functions.
Using this model setup, we confirmed in vivo the inhibitory action of huiPS-MSCs cells on the proliferation of T cells since we observed a decreased expansion of the CD3+ T-cell population in huiPS-MSC-injected mice. Even if this impact appears to be more pronounced on the CD8+ than CD4+ T-cell populations, both T-cell populations were affected.
Interestingly, in the case of allogenic stem cells transplantation, MSC-treated patients presented a higher level of IL-2 in their serum and a higher Th2 cytokine (IL4) profile at the expense of the Th1 cytokine (IFNγ) profile (18). Our results indicate that treatment with the huiPS-MSCs induces a switch from a Th1 signature toward a regulatory signature (with increased IL-10 production) and the generation of FoxP3+ Treg cells. Nevertheless, not all clinical studies using MSC infusion in human reported such clear shifts in T-cell responses, possibly due to different clinical settings. Our results highlight that the induction of Treg cells may be a substantial mechanism by which huiPS-MSCs and probably adult MSCs exert their function in vivo. Interestingly, Gregoire-Gauthier et al. (69) reported that cord blood-derived MSCs were able to delayed clinical sign of acute GVHD in irradiated NSG mice through healing process and immunomodulation not related to Treg cells. This supports that the function of MSCs may also differ depending on the experimental settings and this might explain some of the contradictory results of clinical studies.
Co-transplantation of MSCs during allogeneic hematopoietic stem cell transplantation has been explored to enhance engraftment and decrease the risk of graft-versus-host disease (GVHD). However, although several preclinical and clinical studies with MSCs have been conducted, the results have been mixed and the efficacy of MSCs in a transplantation setting is so far unclear (14–19, 70). For such clinical studies, the MSC source and their characteristics should be clearly defined to induce reproducible responses on T immunosuppression. Such standardization could be potentiated with in vitro generated MSCs, and our simple method could therefore be very useful.
To the best of our knowledge, our results represent the first demonstration that immune-modulatory huiPS-MSCs act on human T lymphocytes in vivo through a switch from a Th1 inflammatory differentiation pathway to a Treg cell pathway. These findings may promote the development of new strategies, involving pluripotent stem cells and their derived cells, for the induction of specific immune tolerance.
This study was carried out in accordance with the recommendations of our local Institutional Ethic Committee for Laboratory Animals (CIEPAL-Azur, NCE/2013-102), France. The protocol was approved by the C3M animal core facility committee (INSERM U1065, Université de Nice, France).
CR: collection and/or assembly of data, data analysis and interpretation, manuscript writing, and final approval of manuscript. GS, JP, and LI: collection and/or assembly of data, data analysis and interpretation, and final approval of manuscript. NB, GD, CV, and AB: collection and/or assembly of data and final approval of manuscript. NM and AW: data analysis and interpretation and final approval of manuscript. CB-W: data analysis and interpretation, financial support, and final approval of manuscript. MR: conception and design, financial support, collection and/or assembly of data, data analysis and interpretation, manuscript writing, and final approval of manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The authors sincerely thank Dr. I Petit and Pr. D Aberdam (INSERM UMR-S976, Université Paris Diderot, Paris, France) as well as Dr. S Bendahhou (CNRS-UMR 7370, Université de Nice, Nice, France) for providing us with the different human iPS cell lines that were used in this study, and Dr. Arieh Moussaieff (School of Pharmacy, Institute for Drug Research, Hebrew University of Jerusalem, Jerusalem, Israel) for fruitful discussion on human iPS in vitro fate. They also thank the C3M animal core facility, INSERM U1065, Université de Nice, France.
This work was supported by the «Association Française contre les Myopathies (AFM)—Téléthon CLT/SS/2013-1036/no. 15599», the «Fondation pour la Recherche Médicale DEQ 20130326467», and the «Groupe Pasteur Mutualité no 097051».
The Supplementary Material for this article can be found online at http://www.frontiersin.org/articles/10.3389/fimmu.2017.01991/full#supplementary-material.
2. Horwitz EM, Le Blanc K, Dominici M, Mueller I, Slaper-Cortenbach I, Marini FC, et al. Clarification of the nomenclature for MSC: the International Society for Cellular Therapy position statement. Cytotherapy (2005) 7:393–5. doi:10.1080/14653240500319234
3. Dominici M, Le Blanc K, Mueller I, Slaper-Cortenbach I, Marini F, Krause D, et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy (2006) 8:315–7. doi:10.1080/14653240600855905
5. Augello A, Tasso R, Negrini SM, Amateis A, Indiveri F, Cancedda R, et al. Bone marrow mesenchymal progenitor cells inhibit lymphocyte proliferation by activation of the programmed death 1 pathway. Eur J Immunol (2005) 35:1482–90. doi:10.1002/eji.200425405
6. Xue Q, Luan X-Y, Gu Y-Z, Wu H-Y, Zhang G-B, Yu G-H, et al. The negative co-signaling molecule B7-H4 is expressed by human bone marrow-derived mesenchymal stem cells and mediates its T-cell modulatory activity. Stem Cells Dev (2010) 19:27–38. doi:10.1089/scd.2009.0076
7. Selmani Z, Naji A, Zidi I, Favier B, Gaiffe E, Obert L, et al. Human leukocyte antigen-G5 secretion by human mesenchymal stem cells is required to suppress T lymphocyte and natural killer function and to induce CD4+CD25highFOXP3+ regulatory T cells. Stem Cells (2008) 26:212–22. doi:10.1634/stemcells.2007-0554
8. Melief SM, Schrama E, Brugman MH, Tiemessen MM, Hoogduijn MJ, Fibbe WE, et al. Multipotent stromal cells induce human regulatory T cells through a novel pathway involving skewing of monocytes toward anti-inflammatory macrophages: MSC induce Tregs through skewing of monocytes. Stem Cells (2013) 31:1980–91. doi:10.1002/stem.1432
9. Noort WA, Kruisselbrink AB, in’t Anker PS, Kruger M, van Bezooijen RL, de Paus RA, et al. Mesenchymal stem cells promote engraftment of human umbilical cord blood-derived CD34+ cells in NOD/SCID mice. Exp Hematol (2002) 30:870–8. doi:10.1016/S0301-472X(02)00820-2
10. Maitra B, Szekely E, Gjini K, Laughlin MJ, Dennis J, Haynesworth SE, et al. Human mesenchymal stem cells support unrelated donor hematopoietic stem cells and suppress T-cell activation. Bone Marrow Transplant (2004) 33:597–604. doi:10.1038/sj.bmt.1704400
11. Polchert D, Sobinsky J, Douglas G, Kidd M, Moadsiri A, Reina E, et al. IFN-gamma activation of mesenchymal stem cells for treatment and prevention of graft versus host disease. Eur J Immunol (2008) 38:1745–55. doi:10.1002/eji.200738129
13. Yin F, Battiwalla M, Ito S, Feng X, Chinian F, Melenhorst JJ, et al. Bone marrow mesenchymal stromal cells to treat tissue damage in allogeneic stem cell transplant recipients: correlation of biological markers with clinical responses: MSC transplantation biomarkers. Stem Cells (2014) 32:1278–88. doi:10.1002/stem.1638
14. Le Blanc K, Rasmusson I, Sundberg B, Gotherstrom C, Hassan M, Uzunel M, et al. Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells. Lancet (2004) 363:1439–41. doi:10.1016/S0140-6736(04)16104-7
15. Le Blanc K, Frassoni F, Ball L, Locatelli F, Roelofs H, Lewis I, et al. Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease: a phase II study. Lancet (2008) 371:1579–86. doi:10.1016/S0140-6736(08)60690-X
16. von Bahr L, Sundberg B, Lönnies L, Sander B, Karbach H, Hägglund H, et al. Long-term complications, immunologic effects, and role of passage for outcome in mesenchymal stromal cell therapy. Biol Blood Marrow Trans (2012) 18:557–64. doi:10.1016/j.bbmt.2011.07.023
17. Ball LM, Bernardo ME, Roelofs H, van Tol MJ, Contoli B, Zwaginga JJ, et al. Multiple infusions of mesenchymal stromal cells induce sustained remission in children with steroid-refractory, grade III-IV acute graft-versus-host disease. Br J Haematol (2013) 163(4):501–9. doi:10.1111/bjh.12545
18. Jitschin R, Mougiakakos D, Von Bahr L, Volkl S, Moll G, Ringden O, et al. Alterations in the cellular immune compartment of patients treated with third-party mesenchymal stromal cells following allogeneic hematopoietic stem cell transplantation. Stem Cells (2013) 31:1715–25. doi:10.1002/stem.1386
19. te Boome LCJ, Mansilla C, van der Wagen LE, Lindemans CA, Petersen EJ, Spierings E, et al. Biomarker profiling of steroid-resistant acute GVHD in patients after infusion of mesenchymal stromal cells. Leukemia (2015) 29:1839–46. doi:10.1038/leu.2015.89
20. Chen YS, Pelekanos RA, Ellis RL, Horne R, Wolvetang EJ, Fisk NM. Small molecule mesengenic induction of human induced pluripotent stem cells to generate mesenchymal stem/stromal cells. Stem Cells Transl Med (2012) 1(2):83–95. doi:10.5966/sctm.2011-0022
22. Li O, Tormin A, Sundberg B, Hyllner J, Le Blanc K, Scheding S. Human embryonic stem cell-derived mesenchymal stroma cells (hES-MSCs) engraft in vivo and support hematopoiesis without suppressing immune function: implications for off-the shelf ES-MSC therapies. PLoS One (2013) 8(1):e55319. doi:10.1371/journal.pone.0055319
23. Deng P, Zhou C, Alvarez R, Hong C, Wang CY. Inhibition of IKK/NF-kappaB signaling enhances differentiation of mesenchymal stromal cells from human embryonic stem cells. Stem Cell Reports (2016) 6(4):456–65. doi:10.1016/j.stemcr.2016.02.006
24. Lian Q, Zhang Y, Zhang J, Zhang HK, Wu X, Zhang Y, et al. Functional mesenchymal stem cells derived from human induced pluripotent stem cells attenuate limb ischemia in mice. Circulation (2010) 121(9):1113–23. doi:10.1161/CIRCULATIONAHA.109.898312
25. Wang X, Lazorchak AS, Song L, Li E, Zhang Z, Jiang B, et al. Immune modulatory mesenchymal stem cells derived from human embryonic stem cells through a trophoblast-like stage. Stem Cells (2016) 34(2):380–91. doi:10.1002/stem.2242
26. Giuliani M, Oudrhiri N, Noman ZM, Vernochet A, Chouaib S, Azzarone B, et al. Human mesenchymal stem cells derived from induced pluripotent stem cells down-regulate NK-cell cytolytic machinery. Blood (2011) 118(12):3254–62. doi:10.1182/blood-2010-12-325324
27. Fu QL, Chow YY, Sun SJ, Zeng QX, Li HB, Shi JB, et al. Mesenchymal stem cells derived from human induced pluripotent stem cells modulate T-cell phenotypes in allergic rhinitis. Allergy (2012) 67(10):1215–22. doi:10.1111/j.1398-9995.2012.02875.x
28. Wang X, Kimbrel EA, Ijichi K, Paul D, Lazorchak AS, Chu J, et al. Human ESC-derived MSCs outperform bone marrow MSCs in the treatment of an EAE model of multiple sclerosis. Stem Cell Reports (2014) 3(1):115–30. doi:10.1016/j.stemcr.2014.04.020
29. Petit I, Kesner NS, Karry R, Robicsek O, Aberdam E, Muller FJ, et al. Induced pluripotent stem cells from hair follicles as a cellular model for neurodevelopmental disorders. Stem Cell Res (2012) 8(1):134–40. doi:10.1016/j.scr.2011.09.003
31. Ciucci T, Ibanez L, Boucoiran A, Birgy-Barelli E, Pene J, Abou-Ezzi G, et al. Bone marrow Th17 TNFalpha cells induce osteoclast differentiation, and link bone destruction to IBD. Gut (2015) 64(7):1072–81. doi:10.1136/gutjnl-2014-306947
32. Shao K, Koch C, Gupta MK, Lin Q, Lenz M, Laufs S, et al. Induced pluripotent mesenchymal stromal cell clones retain donor-derived differences in DNA methylation profiles. Mol Ther (2013) 21(1):240–50. doi:10.1038/mt.2012.207
33. Diederichs S, Tuan RS. Functional comparison of human-induced pluripotent stem cell-derived mesenchymal cells and bone marrow-derived mesenchymal stromal cells from the same donor. Stem Cells Dev (2014) 23(14):1594–610. doi:10.1089/scd.2013.0477
34. Kimbrel EA, Kouris NA, Yavanian GJ, Chu J, Qin Y, Chan A, et al. Mesenchymal stem cell population derived from human pluripotent stem cells displays potent immunomodulatory and therapeutic properties. Stem Cells Dev (2014) 23(14):1611–24. doi:10.1089/scd.2013.0554
35. Cheng PP, Liu XC, Ma PF, Gao C, Li JL, Lin YY, et al. iPSC-MSCs combined with low-dose rapamycin induced islet allograft tolerance through suppressing Th1 and enhancing regulatory T-cell differentiation. Stem Cells Dev (2015) 24(15):1793–804. doi:10.1089/scd.2014.0488
37. Hewitt KJ, Shamis Y, Carlson MW, Aberdam E, Aberdam D, Garlick JA. Three-dimensional epithelial tissues generated from human embryonic stem cells. Tissue Eng Part A (2009) 15(11):3417–26. doi:10.1089/ten.TEA.2009.0060
38. Shalom-Feuerstein R, Serror L, De La Forest Divonne S, Petit I, Aberdam E, Camargo L, et al. Pluripotent stem cell model reveals essential roles for miR-450b-5p and miR-184 in embryonic corneal lineage specification. Stem Cells (2012) 30(5):898–909. doi:10.1002/stem.1068
39. Chen L, Tredget EE, Wu PY, Wu Y. Paracrine factors of mesenchymal stem cells recruit macrophages and endothelial lineage cells and enhance wound healing. PLoS One (2008) 3(4):e1886. doi:10.1371/journal.pone.0001886
40. Pricola KL, Kuhn NZ, Haleem-Smith H, Song Y, Tuan RS. Interleukin-6 maintains bone marrow-derived mesenchymal stem cell stemness by an ERK1/2-dependent mechanism. J Cell Biochem (2009) 108(3):577–88. doi:10.1002/jcb.22289
41. Ito R, Katano I, Kawai K, Hirata H, Ogura T, Kamisako T, et al. Highly sensitive model for xenogenic GVHD using severe immunodeficient NOG mice. Transplantation (2009) 87:1654–8. doi:10.1097/TP.0b013e3181a5cb07
42. Takahashi K, Tanabe K, Ohnuki M, Narita M, Ichisaka T, Tomoda K, et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell (2007) 131:861–72. doi:10.1016/j.cell.2007.11.019
43. Yu J, Vodyanik MA, Smuga-Otto K, Antosiewicz-Bourget J, Frane JL, Tian S, et al. Induced pluripotent stem cell lines derived from human somatic cells. Science (2007) 318:1917–20. doi:10.1126/science.1151526
45. Han MH, Lundgren DH, Jaiswal S, Chao M, Graham KL, Garris CS, et al. Janus-like opposing roles of CD47 in autoimmune brain inflammation in humans and mice. J Exp Med (2012) 209(7):1325–34. doi:10.1084/jem.20101974
46. Workman CJ, Cauley LS, Kim IJ, Blackman MA, Woodland DL, Vignali DA. Lymphocyte activation gene-3 (CD223) regulates the size of the expanding T cell population following antigen activation in vivo. J Immunol (2004) 172(9):5450–5. doi:10.4049/jimmunol.172.9.5450
48. Walunas TL, Lenschow DJ, Bakker CY, Linsley PS, Freeman GJ, Green JM, et al. CTLA-4 can function as a negative regulator of T cell activation. Immunity (1994) 1(5):405–13. doi:10.1016/1074-7613(94)90071-X
51. Liu W, Putnam AL, Xu-Yu Z, Szot GL, Lee MR, Zhu S, et al. CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4+ T reg cells. J Exp Med (2006) 203(7):1701–11. doi:10.1084/jem.20060772
53. Horwitz DA, Zheng SG, Gray JD. Natural and TGF-beta-induced Foxp3(+)CD4(+) CD25(+) regulatory T cells are not mirror images of each other. Trends Immunol (2008) 29(9):429–35. doi:10.1016/j.it.2008.06.005
55. Thornton AM, Korty PE, Tran DQ, Wohlfert EA, Murray PE, Belkaid Y, et al. Expression of Helios, an Ikaros transcription factor family member, differentiates thymic-derived from peripherally induced Foxp3+ T regulatory cells. J Immunol (2010) 184(7):3433–41. doi:10.4049/jimmunol.0904028
59. Szurek E, Cebula A, Wojciech L, Pietrzak M, Rempala G, Kisielow P, et al. Differences in expression level of Helios and neuropilin-1 do not distinguish thymus-derived from extrathymically-induced CD4+Foxp3+ regulatory T cells. PLoS One (2015) 10(10):e0141161. doi:10.1371/journal.pone.0141161
60. Elkord E. Helios should not be cited as a marker of human thymus-derived Tregs. commentary: helios(+) and helios(-) cells coexist within the natural FOXP3(+) T regulatory cell subset in humans. Front Immunol (2016) 7:276. doi:10.3389/fimmu.2016.00276
63. Zheng SG, Wang J, Horwitz DA. Cutting edge: Foxp3+CD4+CD25+ regulatory T cells induced by IL-2 and TGF-beta are resistant to Th17 conversion by IL-6. J Immunol (2008) 180(11):7112–6. doi:10.4049/jimmunol.180.11.7112
65. King MA, Covassin L, Brehm MA, Racki W, Pearson T, Leif J, et al. Human peripheral blood leucocyte non-obese diabetic-severe combined immunodeficiency interleukin-2 receptor gamma chain gene mouse model of xenogeneic graft-versus-host-like disease and the role of host major histocompatibility complex. Clin Exp Immunol (2009) 157(1):104–18. doi:10.1111/j.1365-2249.2009.03933.x
66. Ali N, Flutter B, Sanchez Rodriguez R, Sharif-Paghaleh E, Barber LD, Lombardi G, et al. Xenogeneic graft-versus-host-disease in NOD-scid IL-2Rgammanull mice display a T-effector memory phenotype. PLoS One (2012) 7(8):e44219. doi:10.1371/journal.pone.0044219
67. Tobin LM, Healy ME, English K, Mahon BP. Human mesenchymal stem cells suppress donor CD4(+) T cell proliferation and reduce pathology in a humanized mouse model of acute graft-versus-host disease. Clin Exp Immunol (2013) 172(2):333–48. doi:10.1111/cei.12056
68. Lee RH, Pulin AA, Seo MJ, Kota DJ, Ylostalo J, Larson BL, et al. Intravenous hMSCs improve myocardial infarction in mice because cells embolized in lung are activated to secrete the anti-inflammatory protein TSG-6. Cell Stem Cell (2009) 5(1):54–63. doi:10.1016/j.stem.2009.05.003
69. Gregoire-Gauthier J, Selleri S, Fontaine F, Dieng MM, Patey N, Despars G, et al. Therapeutic efficacy of cord blood-derived mesenchymal stromal cells for the prevention of acute graft-versus-host disease in a xenogenic mouse model. Stem Cells Dev (2012) 21(10):1616–26. doi:10.1089/scd.2011.0413
70. Kallekleiv M, Larun L, Bruserud O, Hatfield KJ. Co-transplantation of multipotent mesenchymal stromal cells in allogeneic hematopoietic stem cell transplantation: a systematic review and meta-analysis. Cytotherapy (2016) 18(2):172–85. doi:10.1016/j.jcyt.2015.11.010
Keywords: induced pluripotent stem cells, mesenchymal stromal cells, human T-cell immunosuppression, regulatory T cells, humanized NSG mouse, tolerance
Citation: Roux C, Saviane G, Pini J, Belaïd N, Dhib G, Voha C, Ibáñez L, Boutin A, Mazure NM, Wakkach A, Blin-Wakkach C and Rouleau M (2018) Immunosuppressive Mesenchymal Stromal Cells Derived from Human-Induced Pluripotent Stem Cells Induce Human Regulatory T Cells In Vitro and In Vivo. Front. Immunol. 8:1991. doi: 10.3389/fimmu.2017.01991
Received: 04 September 2017; Accepted: 21 December 2017;
Published: 25 January 2018
Edited by:Song Guo Zheng, Penn State Milton S. Hershey Medical Center, United States
Reviewed by:Hans-Dieter Volk, Charité – University Medicine, Germany
Baojun Zhang, Duke University, United States
Copyright: © 2018 Roux, Saviane, Pini, Belaïd, Dhib, Voha, Ibáñez, Boutin, Mazure, Wakkach, Blin-Wakkach and Rouleau. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Matthieu Rouleau, firstname.lastname@example.org
†Present address: Clémence Roux, Service d’Oncologie-Hématologie Pédiatrique, APHM, Marseille, France;
Jonathan Pini, Centre for Regenerative Medicine – MGH, Boston, MA, United States