Regulatory T cells (Treg cells), which have abundant expression of the interleukin 2 receptor (IL-2R), are reliant on IL-2 produced by activated T cells. This feature indicates a key role for a simple network based on the consumption of IL-2 by Treg cells in their suppressor function. However, congenital deficiency in IL-2R results in reduced expression of the Treg cell lineage–specification factor Foxp3, which has confounded experimental efforts to understand the role of IL-2R expression and signaling in the suppressor function of Treg cells. Using genetic gain- and loss-of-function approaches, we found that capture of IL-2 was dispensable for the control of CD4+ T cells but was important for limiting the activation of CD8+ T cells, and that IL-2R-dependent activation of the transcription factor STAT5 had an essential role in the suppressor function of Treg cells separable from signaling via the T cell antigen receptor.
Regulatory T cells (Treg cells) that express the transcription factor Foxp3 restrain immune responses to self and foreign antigens1,2,3. Treg cells have abundant expression of the interleukin 2 receptor α-chain (IL-2Rα; CD25) but are unable to produce IL-2. IL-2 binds with low affinity to IL-2Rα or to heterodimers of the common γ-chain (γc; CD132) and IL-2Rβ (CD122), but receptor affinity increases ∼1,000-fold when these three subunits collectively interact with IL-2 (ref. 4). IL-2 and the transcription factor STAT5, a key target downstream of JAK kinases associated with IL-2R, are indispensable for inducing the expression of Foxp3 and differentiation of Treg cells in the thymus5,6,7,8,9,10,11. IL-2Rβ and γc are shared with the IL-15 receptor, whose signaling can also contribute to the induction of Foxp3 expression12. IL-2, in cooperation with the cytokine TGF-β, is also required for extrathymic Treg cell differentiation13.
While the role of IL-2R signaling in the induction of Foxp3 expression and Treg cell differentiation in the thymus is well established, the importance of IL-2R expression in mature Treg cells is not well understood. Although deficiency in STAT5 abolishes Foxp3 expression, it can be restored by increased amounts of the anti-apoptotic molecule Bcl2. That finding raised the possibility that a chief role of IL-2 might be in the survival of differentiating Treg cells or their precursors14. It has also been reported that ablation of the pro-apoptotic protein Bim can rescue Treg cells or their precursors from apoptosis associated with deficiency in IL-2 or IL-2R and restore the number of Treg cells, but it does not prevent fatal autoimmunity15. However, a profound effect of congenital deficiency in IL-2, Bcl2 and Bim on the differentiation and selection of Treg cells and self-reactive effector T cells (Teff cells) has confounded interpretation of that observation. Antibody-mediated neutralization of IL-2 in adult mice that have undergone removal of the thymus reduces the number of Treg cells and Foxp3 expression in Treg cells16,17. Thus, IL-2 supports stability of the Treg cell lineage after differentiation18,19. However, expression of a transgene encoding IL-2Rβ exclusively in thymocytes has been reported to rescue Il2rb−/− mice from lethal autoimmune disease, which suggests that IL-2R expression is dispensable in peripheral Treg cells7,11. Thus, a role for IL-2R expression and signaling in peripheral Treg cells has remained uncertain. Hypothetically, a role for IL-2R in peripheral Treg cells could be threefold: guidance for Treg cells to sense their targets, which are activated self-reactive T cells that serve as a source of IL-2; Treg cell–mediated deprivation of IL-2 as a mechanism of suppression; and cell-intrinsic IL-2 signaling in differentiated Treg cells to support their maintenance, proliferation or function due to triggering of JAK–STAT5, PI3K–Akt or Ras–ERK signaling pathways. Previous studies have focused mainly on the induction or maintenance of Foxp3, while other aspects of IL-2R function have not been firmly established due to the aforementioned limitations.
Despite their considerable reliance on IL-2 for the maintenance of Foxp3 expression, Treg cells are unable to produce IL-2. The reason for the inhibition of autologous activation of STAT5 in Treg cells and the potential biological importance of this IL-2-based Treg cell–Teff cell regulatory loop also remain unknown. It has been suggested that repression of IL-2 is needed to maintain the 'unbound' state of high-affinity IL-2R on Treg cells, and unbound IL-2R serves a key role in Treg cell–mediated suppression by depriving Teff cells of IL-2 (refs. 20,21,22,23,24); however, whether this mechanism has a non-redundant role in suppression in vivo is unknown. To address the role of IL-2R and downstream signaling pathways in differentiated Treg cells, we ablated IL-2Rα, IL-2Rβ and STAT5 in Foxp3-expressing cells. By simultaneously inducing expression of an active form of STAT5, we assessed the differential requirements for IL-2R expression and IL-2 signaling in Treg cell homeostasis versus Treg cell suppressor activity.
IL-2R is indispensable for Treg cell function
To definitively establish a role for IL-2R in Treg cell function in vivo, we generated mice with Treg cell–specific conditional knockout of IL-2Rβ by using Cre recombinase driven by the endogenous Foxp3 locus (Foxp3Cre) to delete loxP-flanked Il2rb alleles (Il2rbfl/fl) in Treg cells after Foxp3 was expressed. Il2rbfl/flFoxp3Cre mice developed systemic fatal autoimmune inflammatory lesions and lymphoproliferation, albeit somewhat milder than that observed in mice with germline Foxp3 deficiency3 (Fig. 1a–c). The expression of IL-2Rβ and IL-2Rα was lower in Il2rbfl/flFoxp3Cre peripheral Treg cells than in their Il2rbfl/wtFoxp3Cre counterparts (Fig. 1d), and tyrosine-phosphorylation of STAT5 in response to IL-2 was lacking in Il2rbfl/flFoxp3Cre peripheral Treg cells (Fig. 1e). The frequency of Foxp3+ cells among CD4+ T cells and the expression of Foxp3 on a per-cell basis were both lower in Il2rbfl/flFoxp3Cre mice than in Il2rbfl/wtFoxp3Cre mice (Fig. 1f). In healthy Il2rbfl/flFoxp3Cre/wt female mice, in which IL-2Rβ-sufficient Treg cells and IL-2Rβ-deficient Treg cells co-exist due to random inactivation of the X chromosome, IL-2Rβ-deficient Treg cells were under-represented (Fig. 1g,h). It has been suggested that IL-2 is selectively required for the maintenance of CD62LhiCD44lo Treg cells but is dispensable for CD62LloCD44hi Treg cells25. However, we found that the abundance of both CD62LhiCD44lo Treg cells and CD62LloCD44hi Treg cells was significantly lower in the absence of IL-2Rβ than in its presence in healthy Il2rbfl/flFoxp3Cre/wt female mice (Supplementary Fig. 1a). In these mice, IL-2Rβ-deficient (Il2rbfl/flFoxp3Cre/wt) Treg cells had lower expression of Foxp3 and the Treg cell 'signature' molecules IL-2Rα, CTLA-4, GITR and CD103 than that of IL-2Rβ-sufficient (Il2rbfl/wtFoxp3Cre/wt) Treg cells regardless of their expression of CD62L and CD44 (Fig. 1i,j and Supplementary Fig. 1a). Although in diseased Il2rbfl/flFoxp3Cre mice, the majority of Treg cells were CD62LloCD44hi, this was probably a consequence of severe inflammation, because the frequency of Treg cells was also much lower in Il2rbfl/flFoxp3Cre mice than in Il2rbfl/wtFoxp3Cre mice at sites at which CD62LloCD44hi cells were prevalent—i.e., the small and large intestines (Supplementary Fig. 1b). Accordingly, the expression of many characteristic Treg cell markers, except for CD25 and Foxp3, was upregulated as the result of Treg cell activation in Il2rbfl/flFoxp3Cre mice (Supplementary Fig. 1c). These observations suggested that both the CD62LhiCD44lo Treg cell subset and the CD62LloCD44hi Treg cell subset, including those residing in non-lymphoid tissues, were dependent on IL-2, although under inflammatory conditions the latter was sustained to some extent by IL-2R-independent signals. Despite their upregulation of the expression of CTLA-4, GITR, the costimulatory receptor ICOS and CD103, the 'activated' IL-2Rβ-deficient Treg cells from Il2rbfl/flFoxp3Cre mice were still unable to control inflammation in the diseased mice and were not suppressive when transferred together with Teff cells into lymphopenic recipients (data not shown).
Our findings raised the question whether ablation of IL-2Rα (which, in addition to facilitating IL-2 signaling, enables its sequestration from Teff cells) would result in Treg cell deficiency and disease similar to that of Il2rbfl/flFoxp3Cre mice. Thus, we generated mice with a loxP-flanked Il2ra allele (J.D.F., data not shown) and induced its conditional ablation in Treg cells by means similar to those described above. We found that Treg cell–specific deficiency in IL-2Rα resulted in a disease with an early onset and severity similar to that observed after ablation of IL-2Rβ (Supplementary Fig. 1d–f). Of note, germline deficiency in either Il2ra or Il2rb in mice on the same C57BL6/J strain as that of our mice with conditional knockout resulted in a considerably less aggressive disease with a delayed onset (data not shown), probably due to the role of IL-2R signaling in Teff cells. Our findings also indicated that IL-15 was unable to effectively compensate for the loss of IL-2 signaling in differentiated Treg cells, because in Il2rafl/flFoxp3Cre mice, Treg cells lacked only signaling via IL-2, whereas in Il2rbfl/flFoxp3Cre mice, they lacked signaling via both IL-2 and IL-15, yet they were affected similarly. This was in contrast to Treg cell differentiation in the thymus, in which IL-15 can contribute in part to Foxp3 induction12.
Since IL-2R activates PI3K–Akt, MAPK, and JAK–STAT5 signaling pathways, we next sought to assess the role of STAT5 activation downstream of IL-2R signaling in Treg cells. We found that ablation of STAT5 impaired Treg cell function similarly to ablation of IL-2Rβ and that Stat5afl/flStat5bfl/flFoxp3Cre mice were affected by fatal autoimmunity in a way similar to that of mice harboring IL-2R-deficient Treg cells (Supplementary Fig. 1g–k). Thus, in agreement with IL-2-neutralization studies, these results indicated that IL-2R signaling was required for Treg cell fitness in a cell-intrinsic manner.
Restoring STAT5 signaling in IL-2R-deficient Treg cells
The findings reported above indicated that activation of STAT5 downstream of IL-2R was continuously required for Treg cell function. However, the marked decrease in IL-2R expression observed in STAT5-deficient Treg cells (Supplementary Fig. 1g) made it impossible to separate loss of STAT5 from impairment in all IL-2R functions (i.e., detection of IL-2, transduction of STAT5-dependent and STAT5-independent signals, and consumption and deprivation of IL-2) as a key contributor to the observed severe dysfunction of Treg cells.
To address that major caveat and to understand the role of STAT5 versus that of IL-2R, we sought to determine whether expression of a gain-of-function form of STAT5b was able to restore Treg cell function in the absence of IL-2R. A published study using a transgene encoding a constitutively active form of STAT5b (STAT5b-CA) driven by the proximal promoter of the gene encoding the kinase Lck in the absence of IL-2Rβ showed restoration of Treg cell differentiation in the thymus but not rescue from lymphoproliferative syndrome9. However, the expression of this transgene early during thymopoiesis leads to leukemic lymphoproliferation, which complicated the interpretation of those findings. In addition, both the activity of the proximal Lck promoter and the expression of the transgene became lower over time in peripheral T cells in these mice9. Therefore, we generated a gene-targeted mouse strain using the Rosa26 'gene-trap' locus26 in which a transgene encoding STAT5b-CA driven by a CAG promoter (chicken β-actin promoter with cytomegalovirus enhancers)27 is preceded by a loxP-flanked STOP cassette (Supplementary Fig. 2a). In the resulting Rosa26Stat5bCA mice, STAT5b-CA is expressed only when the loxP sites undergo Cre-mediated recombination. Introduction of the Rosa26Stat5bCA allele into Il2rbfl/flFoxp3Cre mice and the consequent expression of STAT5b-CA in IL-2Rβ-deficient Treg cells rescued the mice from the systemic inflammation and early fatal disease (Supplementary Fig. 2b). In these mice, the frequency and number of Treg cells were comparable to or even surpassed those in IL-2R-sufficient Il2rbwt/wtFoxp3Cre mice (Fig. 2a). Notably, the expression of IL-2Rα was higher in Treg cells from Rosa26Stat5bCAIl2rbfl/flFoxp3Cre mice than in those from Il2rbfl/flFoxp3Cre or Il2rbwt/wtFoxp3Cre mice, despite the absence of the IL-2Rβ chain (Fig. 2a), which suggested that the expression of IL-2Rα on Treg cells was controlled mainly by STAT5-dependent signaling but not by STAT5-independent signaling. Notably, these IL-2Rβ-deficient Treg cells with heightened IL-2Rα expression remained unresponsive to IL-2 (Fig. 2b).
The observed restoration of the suppressor function of IL-2Rβ-deficient Treg cells and rescue from the early fatal disease via expression of STAT5b-CA raised the possibility that the reintroduced high levels of IL-2Rα were responsible for these effects. However, expression of STAT5b-CA similarly rescued Il2rafl/flFoxp3Cre mice from the early fatal disease (Supplementary Fig. 2c–h). Notably, although the impaired ability of Treg cells to capture and consume IL-2 in both Il2rbfl/flFoxp3Cre mice and Il2rafl/flFoxp3Cre mice was not 'rescued' via expression of STAT5b-CA (Fig. 2c), the reactivity of CD4+ T cells was fully controlled in these mice (Fig. 2d and Supplementary Fig. 2d–h). These results suggested that the ability to capture and compete for IL-2 was dispensable for Treg cell–mediated suppression of CD4+ T cell responses. In contrast, however, the population expansion of CD8+ T cells, in particular that of activated CD62LhiCD44hi CD8+ T cells, was restrained only marginally in these mice (Fig. 2d and Supplementary Fig. 2f,h). Although expansion of the CD8+CD62LloCD44hi subset was relatively well controlled, albeit not perfectly controlled, in neonatal mice (Fig. 2d and Supplementary Fig. 2f), this subset also gradually started to expand in these mice as early as 3 weeks after birth (Supplementary Fig. 2i). Although both Rosa26Stat5bCAIl2rbfl/flFoxp3Cre mice and Rosa26Stat5bCAIl2rafl/flFoxp3Cre mice were rescued from premature death and showed substantially improved clinical status comparable to that of healthy controls, they gradually failed to thrive and started to succumb to disease accompanied by massively expanded activated CD62LhiCD44hi and CD62LloCD44hi CD8+ T cell subsets in lymph nodes (LNs) and tissues by approximately 12 weeks of age (Supplementary Fig. 2i,j). These findings raised the possibility that IL-2 consumption by Treg cells, while dispensable for the control of CD4+ T cells, was important for the restraint of CD8+ T cells.
Treg cells suppress CD8+ T cell responses via IL-2 depletion
To determine if the impairment in consumption of IL-2 by Treg cells accounted for the proliferation of CD8+ T cells in Rosa26Stat5bCAIl2rbfl/flFoxp3Cre mice, we administered IL-2-neutralizing antibodies to those mice starting from 5–7 d of age. As IL-2 supports the differentiation of Treg cells in the thymus, neutralization of IL-2 reduced the frequency of Treg cells in all groups of mice and induced immunoactivation in control Il2rbfl/wtFoxp3Cre mice (Fig. 2e and Supplementary Fig. 3a). In Il2rbfl/flFoxp3Cre mice, which spontaneously developed disease, production of the TH2 (T helper type 2) cytokines IL-4 and IL-13 by CD4+ T cells was significantly reduced by neutralization of IL-2; however, the activation of CD4+ and CD8+ T cells was at best reduced only marginally or unaffected. In contrast, the activation and proliferation of CD8+ T cells observed in Rosa26Stat5bCAIl2rbfl/flFoxp3Cre mice was almost completely suppressed by this treatment.
The relative reduction in the CD8+CD62LloCD44hi T cell subset and more pronounced proliferation of CD8+CD62LhiCD44hi T cell subset in Rosa26Stat5bCAIl2rbfl/flFoxp3Cre and Rosa26Stat5bCAIl2rafl/flFoxp3Cre mice raised the possibility that loss of IL-2-consumption by Treg cells might selectively impair their suppression of the population expansion of memory CD8+ T cells but not the recruitment of naive CD8+ T cells into the effector-cell pool. We tested this idea by adoptive transfer of CD4+ and CD8+ cell subsets into lymphopenic recipients. Consistent with observations of Foxp3Cre mice, the impaired suppression of the population expansion and activation of CD4+ T cells by IL-2R-deficient Treg cells was completely 'rescued' by STAT5b-CA; in contrast, their ability to suppress memory CD8+ T cells was not restored, whereas suppression of the population expansion and activation of naive CD8+ T cells was recovered only partially (Fig. 2f). Thus, IL-2 consumption by Treg cells seemed to have a non-redundant role in suppressing the population expansion and activation of both the naive CD8+ T cell subset and memory CD8+ T cell subset, although this mechanism seemed to be particularly prominent in control of the latter subset.
Although the majority of activated CD8+ T cells in Il2rbfl/flFoxp3Cre and Rosa26Stat5bCAIl2rbfl/flFoxp3Cre mice did not have detectable expression of IL-2Rα (Supplementary Fig. 3a), these cells were able to activate STAT5 in response to IL-2, albeit to a lesser extent than that observed in cells expressing IL-2Rα (Supplementary Fig. 3b). A small proportion of activated CD4+ T cells with undetectable IL-2Rα expression also responded to IL-2, but the majority of them did not (Supplementary Fig. 3b). naive T CD8+ cells also responded to IL-2, while naive CD4+ T cells did not (Supplementary Fig. 3b). Thus, both naive CD8+ T cells and activated CD8+ T cells seemed to be more sensitive to IL-2 than were CD4+ T cells, and IL-2 consumption by Treg cells might have markedly affected their activation. A corollary to that idea was that activation of STAT5 in CD8+ T cells but not in CD4+ T cells might render the former resistant to Treg cell–mediated suppression. Thus, we tested the effect of STAT5 activation on the proliferation of CD4+ or CD8+ T cells in the presence of Treg cells. For this purpose, we sorted CD4+Foxp3− and CD8+Foxp3− T cells from Rosa26Stat5bCAFoxp3Cre mice and induced expression of STAT5b-CA in these cells by treating them with recombinant Cre protein containing a membrane-permeable TAT peptide (trans-activating transcriptional activator from human immunodeficiency virus) (TAT-Cre). We adoptively transferred the treated cells into lymphopenic recipients with or without Treg cells. Although treatment with TAT-Cre initially induced STAT5b-CA expression in approximately 30% of the treated CD4+ T cells and CD8+ T cells, more than 95% of CD8+ T cells expressed STAT5b-CA 3 weeks after the cell transfer, whereas STAT5b-CA expressing CD4+ T cells increased their frequency to only 40–50% (Fig. 2g). Notably, STAT5b-CA+CD8+ T cell populations robustly expanded in the presence of either control (Il2rawt/wtFoxp3Cre) Treg cells or STAT5b-CA+ Treg cells (Fig. 2g,h). Although some degree of suppression of STAT5b-CA+CD8+ T cells by Treg cells was still observed, it was very mild compared with the suppression of STAT5b-CA−CD8+ T cells (Fig. 2h). In contrast, the proliferation and cytokine production of activated CD4+ T cells, regardless of the expression of STAT5b-CA, were well controlled by Treg cells (Fig. 2h). These observations suggested that STAT5 activation in CD8+ T cells prompted robust population expansion of cells and conferred pronounced resistance to Treg cell–mediated suppression, but STAT5 activation in CD4+ T cells did not. Consistent with those findings, gain-of-function experiments in which IL-2 was provided in the form of immunocomplexes of IL-2 and antibody to IL-2 showed population expansion of CD8+ T cells and CD4+ Treg cells but not of CD4+ Teff cells28. Thus, while the ability to capture and compete for IL-2 was dispensable for Treg cell–mediated suppression of CD4+ T cell responses, this mode of suppression appeared to be essential for the control of CD8+ T cells, which responded to excessive IL-2 more robustly than did CD4+ T cells.
STAT5 activation in Treg cells boosts immunosuppression
The lack of detectable STAT5 activation in response to IL-2 and of STAT5b-CA-driven population expansion of IL-2R-sufficient Treg cells that escaped Cre-mediated recombination (counter-selection) in both Rosa26Stat5bCAIl2rbfl/flFoxp3Cre mice and Rosa26Stat5bCAIl2rafl/flFoxp3Cre mice indicated that the expression of an active form of STAT5 relieved Treg cells from their dependence on IL-2 signaling. This finding offered a unique opportunity to explore the biological importance of the aforementioned IL-2-dependent Treg cell–Teff cell regulatory network by uncoupling Treg cell function from IL-2 production by Teff cells. To address this issue, we generated Rosa26Stat5bCAFoxp3Cre–ERT2 mice, with tamoxifen-inducible expression of STAT5b-CA in differentiated Treg cells (via the tamoxifen-sensitive estrogen receptor variant ERT2)17. Induction of STAT5b-CA expression in ∼20–30% of Treg cells by a single administration of tamoxifen was followed by their rapid increase in number at the expense of Treg cells with a non-recombined Rosa26Stat5bCA allele (Supplementary Fig. 4a,b). It was notable that these cells exhibited a highly diverse use of the T cell antigen receptor (TCR) β-chain variable region similar to that in Rosa26wtFoxp3Cre-ERT2 (control) mice (Supplementary Fig. 4c). The experimental Rosa26Stat5bCAFoxp3Cre-ERT2 mice remained healthy (Supplementary Fig. 4d,e). In these mice, the proliferated STAT5b-CA+ Treg cell population had larger amounts of Foxp3, CD25, CTLA-4 and GITR than those in STAT5b-CA− Treg cells in tamoxifen-treated Rosa26wtFoxp3Cre-ERT2 mice and had a higher proportion of CD62LhiCD44hi cells than CD62LhiCD44lo cells (Fig. 3a–d and Supplementary Fig. 4f), indicative of a STAT5b-CA–imposed biasing of the Treg cell population toward an activated state or a memory state. Consistent with those possibilities, surface expression of IL-7R, the activation marker KLRG1 and CD103 was higher in STAT5b-CA+ Treg cells in tamoxifen-treated Rosa26Stat5bCAFoxp3Cre-ERT2 mice than in STAT5b-CA− Treg cells in tamoxifen-treated Rosa26wtFoxp3Cre-ERT2 mice (Fig. 3d). Notably, in the LNs and Peyer's patches, the number of Treg cells did not increase after the administration of tamoxifen, despite the predominance of STAT5b-CA+ Treg cells in the former mice (Supplementary Fig. 4b,g); this suggested that Treg cells with activated STAT5 'preferentially' distributed in non-lymphoid tissues. The abundance of CD8+Foxp3+ cells also increased after the induction of STAT5b-CA (Supplementary Fig. 4h). The 'autonomous' Treg cells expressing active STAT5 showed heightened in vitro suppressor activity (Supplementary Fig. 4i) and effectively suppressed the basal state of activation and proliferative activity of CD4+ and CD8+ T cells in vivo as well, as indicated by the decreased number of Ki67+ cells and CD62LloCD44hi Teff cells and much larger CD62LhiCD44lo naive T cell pool (Fig. 3e and Supplementary Fig. 5a,b). Accordingly, the production of pro-inflammatory cytokines, most prominently IL-4, by CD4+ T cells and expression of the costimulatory molecules CD80 and CD86 by B cells and dendritic cells (DCs) were reduced after the administration of tamoxifen (Fig. 3f and Supplementary Fig. 5c). These results indicated that expression of STAT5b-CA conferred enhanced suppressor function to Treg cells.
Treg cells have been proposed to promote systemic responses of the TH17 subset of helper T cells and class switching to immunoglobulin A (IgA) in the gut29,30. However, we found that serum and fecal IgA as well as TH17 responses in secondary lymphoid organs were diminished rather than being increased in the presence of STAT5b-CA+ Treg cells (Fig. 3g and Supplementary Fig. 5c). Serum IgM and IgE also showed a tendency toward a decrease, but this was not statistically significant (Supplementary Fig. 5d). These results were in agreement with the increase in TH17 responses and in both TH2-type immunoglobulin class switching and TH1-type immunoglobulin class switching observed upon acute ablation of Treg cells31.
Since altered intestinal immune responses have been linked to the promotion of colonic carcinogenesis, we explored an effect of a gain in Treg cell suppressor function afforded by activated STAT5 in the ApcMin model of colorectal cancer. Mice harboring the ApcMin mutation develop multiple adenomatous polyps in the small intestine32. ApcMinRosa26Stat5bCAFoxp3Cre-ERT2 mice developed a number of polyps similar to or fewer than that of ApcMinFoxp3Cre-ERT2 mice, but the average polyp size was greater in ApcMinRosa26Stat5bCAFoxp3Cre-ERT2 mice than in ApcMinFoxp3Cre-ERT2 mice (Supplementary Fig. 5e). These results were consistent with the idea that suppression of inflammation by Treg cells in tumor microenvironments promotes the growth of tumors once tumors or pre-cancerous lesions are already formed. However, the early stages of colonic carcinogenesis seemed to be not promoted but potentially suppressed by Treg cells with augmented suppressor activity.
In addition to restraining the basal immunological reactivity in physiological settings and modulating colon-carcinoma development, 'autonomous' Treg cells afforded superior protection against autoantigen-induced autoimmunity. We found that at 2–3 months after a single tamoxifen treatment, Rosa26Stat5bCAFoxp3Cre-ERT2 mice were very resistant to experimental autoimmune encephalomyelitis induced by immunization with myelin oligodendrocyte glycoprotein peptide in complete Freund's adjuvant (Fig. 4a–c). The frequency of CD4+Foxp3+ cells was significantly greater in the brain and spinal cord of these mice (Fig. 4b), and the infiltration of inflammatory cells, including neutrophils and IL-17-producing CD4+ TH17 cells, into these organs was significantly lower (Fig. 4c) than that of Foxp3Cre-ERT2 mice. Pathogen-specific responses were also diminished in Rosa26Stat5bCAFoxp3Cre-ERT2 mice relative to those in Foxp3Cre-ERT2 mice (also at 2–3 months after a single tamoxifen treatment). Although Listeria-monocytogenes-specific TH1 responses were suppressed only modestly (Fig. 4d), vaccinia-virus-specific CD8+ T cell responses were markedly reduced in the presence of STAT5b-CA+ Treg cells (Fig. 4e). Our observation of diminished responses to infectious agents and modulation of cancer progression might provide a rationale for why Treg cells lack IL-2 production and autonomous activation of STAT5 and instead are reliant on activated T cells as a source of IL-2.
A distinct role for STAT5 activation in Treg cells
Next we sought to address the question of how sustained STAT5 signaling might potentiate Treg cells' suppressive ability. In genetic loss- and gain-of-function studies, STAT5 activity in Treg cells correlated with their proliferative capacity and expression of IL-2Rα and Foxp3. However, the in vitro suppression assays reported above, as well as the diminished activation of the immune system in the LNs and Peyer's patches of Rosa26Stat5bCAFoxp3Cre-ERT2 mice, in which fewer Treg cells were found than in Foxp3Cre-ERT2 mice, suggested that the enhanced immunosuppression observed in Rosa26Stat5bCAFoxp3Cre-ERT2 mice was not simply due to a numerical increase of Treg cells but that their suppressor activity on a per-cell basis was also augmented. It was also unlikely that mild upregulation of Foxp3 expression in the presence of STAT5b-CA could account for the increased suppressor activity of Treg cells, as genome-wide binding of Foxp3 does not change after Treg cells are activated, which leads to an increase in Foxp3 expression more pronounced than the one caused by STAT5b-CA33. The greater abundance of Foxp3 protein in STAT5b-CA+ Treg cells than in STAT5b-CA− Treg cells was particularly noticeable in the CD25lo Treg cell subset (average difference in mean fluorescence intensity of Foxp3 in Foxp3+ Treg cells from Rosa26Stat5bCAFoxp3Cre-ERT2 mice versus that in those from Foxp3Cre–ERT2 mice (n = 6): CD25hi cells, 1.06-fold; CD25lo cells, 1.36-fold; Fig. 3b), consistent with the observation that STAT5b-CA+ Treg cells were relieved from their dependence on IL-2. Nevertheless, STAT5b-CA+ Treg cells exhibited more potent suppressor function than that of CD25hiFoxp3hi Treg cells from Rosa26wtFoxp3Cre-ERT2 (control) mice when transferred together with Teff cells into lymphopenic recipients, despite comparably high expression of Foxp3 (data not shown). Thus, the enhanced suppressor activity of STAT5b-CA+ Treg cells was probably not due to the increase in Foxp3.
To gain insight into the potential mechanisms underlying the heightened suppressor function conferred by sustained activation of STAT5, we sorted mature Treg cells from Foxp3Cre–ERT2 and Rosa26Stat5bCAFoxp3Cre-ERT2 mice with comparable expression of Foxp3 and analyzed gene expression in these cells by high-throughput sequencing technologies for cDNA (RNA-seq). While the gene-expression profiles of naive CD4+ T cells from both groups of mice were nearly identical, gene expression in Treg cells was markedly affected by the active form of STAT5 (Fig. 5a and Supplementary Fig. 6a). Among all genes expressed (∼11,000) in either the Treg cell populations or naive CD4+ T cell populations analyzed, 342 genes were upregulated and 314 genes were downregulated in STAT5b-CA+ Treg cells relative to their expression in STAT5b-CA− Treg cells (Fig. 5b and Supplementary Fig. 6b). The gene set upregulated in STAT5b-CA+ Treg cells encoded various cell-surface molecules and receptors involved in cell adhesion, migration and cytoskeletal reorganization (Fig. 5c). Several genes that were upregulated or downregulated in STAT5b-CA− Treg cells relative to their expression in naive T cells showed an opposite trend in STAT5b-CA+ Treg cells (Fig. 5c), which suggested that STAT5b-CA did not simply reinforce the Treg cell signature. A published study has shown that exposure of Treg cells to inflammation induced by transient depletion of Treg cells leads to a marked change in their gene expression and a potent increase in their suppressor function33. Consistent with the heightened suppressor function of STAT5b-CA+ Treg cells, we found that the gene-expression changes in these cells conferred by the active form of STAT5 correlated with those found in highly activated Treg cells in inflammatory settings (Fig. 5d). TCR signaling is required for the ability of Treg cells to exert their suppressor function34,35. Thus, it was possible that the TCR- and STAT5-dependent signaling pathways in Treg cells were acting on a largely overlapping set of genes whose expression they jointly regulated to potentiate the suppressor activity of Treg cells. However, our analysis revealed that the gene set affected by the active form of STAT5 was distinct from that expressed in Treg cells in a TCR-dependent manner (Fig. 5d). Thus, both the TCR signaling pathway and STAT5 signaling pathway served an indispensable role in the suppressor activity of Treg cells in vivo by controlling largely distinct sets of genes and probably distinct aspects of Treg cell suppressor activity.
To better understand aspects of Treg cell function potentiated by activation of STAT5, we performed analysis of signaling pathways and molecular-function enrichment. This revealed over-representation of gene sets encoding products involved in cell-cell and extracellular matrix interactions, cell adhesion and cellular locomotion among genes expressed differentially in STAT5b-CA+ Treg cells relative to their expression in STAT5b-CA− Treg cells (Fig. 5e,f and Supplementary Fig. 6c). This result suggested that in Treg cells, activation of STAT5 might potentiate their interactions with the target cells.
Since intravital imaging of Treg cells in vivo has revealed their stable interactions with DCs36, we assessed the potential effect of constitutively active STAT5 in Treg cells on their ability to form conjugates with DCs in vitro. In agreement with the gene-set–enrichment analysis, we found that STAT5b-CA expression in Treg cells promoted the formation of conjugates of Treg cells and DCs (Fig. 6a). These enhanced interactions of STAT5b-CA+ Treg cells with DCs in vitro were consistent with the decreased expression of co-stimulatory molecules by DCs observed in tamoxifen-treated Rosa26Stat5bCAFoxp3Cre-ERT2 mice (Fig. 3f).
The findings reported above raised the question of whether activation of STAT5 can potentiate the suppressor function of Treg cells in a TCR-independent manner. To investigate this, we analyzed Rosa26Stat5bCAFoxp3Cre-ERT2 mice with a Tcrafl allele. Tamoxifen-inducible Cre-mediated ablation of Tcra (and thus the TCR) in Treg cells is highly efficient in these mice and results in activation of the immune system that results from impaired suppressor function34. In heterozygous Tcrafl/wtFoxp3Cre-ERT2 mice, Cre-mediated recombination can theoretically result in ablation of the TCR in up to a half of Treg cells due to allelic exclusion at the Tcra locus. We observed a small proportion of TCR-deficient Treg cells in these mice after 2 weeks of tamoxifen administration (Fig. 6b). Although expression of the active form of STAT5 was observed in ∼50% of TCR-sufficient and TCR-deficient Treg cells in Tcrafl/wtRosa26Stat5bCAFoxp3Cre-ERT2 mice, the proportion of only TCR-sufficient STAT5b-CA+ Treg cells, not TCR-deficient STAT5b-CA+ Treg cells, was greater in these mice than in Tcrafl/wtFoxp3Cre-ERT2 mice (Fig. 6b). The marked increase in T cell activation and pro-inflammatory cytokine production was mitigated in part by expression of the active form of STAT5 in tamoxifen-treated Tcrafl/flRosa26Stat5bCAFoxp3Cre-ERT2 mice (Fig. 6c). This partial recovery of Treg cell suppressor function by the active form of STAT5 in Treg cells that had undergone ablation of the TCR was also confirmed in experiments in which flow-cytometry-sorted TCR-deficient STAT5b-CA+ Treg cells and Teff cells were adoptively transferred into lymphopenic recipients (Fig. 6d). Although the 'rescue' was incomplete, these results suggested that enhanced STAT5 signaling potentiated the suppressor activity of Treg cells in the absence of contemporaneous TCR-dependent signals. Indeed, some features of Treg cells that had been observed in TCR-sufficient STAT5b-CA+ Treg cells were still present in STAT5b-CA+ Treg cells that had undergone TCR ablation (Fig. 6c,d). However, we note that STAT5b-CA expression failed to restore suppressor function in Tcrafl/flRosa26Stat5bCAFoxp3Cre mice in which TCR deletion occurred immediately after the induction of Foxp3 (data not shown). It has been shown that TCR signaling is required for the acquisition of an activated, antigen-experienced phenotype and suppressor function by Treg cells34. Thus, our results suggested that activation of STAT5 potentiated TCR-independent suppressor function in mature Treg cells that had already undergone TCR-dependent maturation. That observation is reminiscent of the sequential requirement for these two signals, via the TCR and IL-2R, in the differentiation of Treg cells in the thymus, where STAT5 signaling promotes differentiation of Treg cell precursors that have experienced permissive TCR signaling37.
Published analysis of mice with germline deficiency in IL-2 and IL-2R subunits have demonstrated that IL-2 is a key cytokine required for the induction of Foxp3 expression and the differentiation of Treg cells in the thymus5,6,7,8,9,10,11. Furthermore, antibody-mediated neutralization of IL-2 and provision of IL-2 in the form of immunocomplexes of IL-2 and antibody to IL-2, as well as genetic delineation of regulatory elements within the Foxp3 locus, have revealed an important role for IL-2 in the maintenance of mature Treg cells and in the stabilization of Foxp3 expression during their extrathymic differentiation16,28,38. Such findings have raised the question of whether IL-2R signaling can also directly promote the suppressor ability of Treg cells and can therefore serve as a critical nexus linking the differentiation and maintenance of Treg cells with their suppressor function. A published in vitro study has proposed a role for IL-2 signaling on the basis of indirect evidence21. In addition, consumption of IL-2 by Treg cells has been suggested to serve an essential role in the suppressor function of Treg cells by causing the death of activated CD4+ T cells due to IL-2 deprivation20,21,22,23,24. On the other hand, other reports have suggested that IL-2R is dispensable for the ability of Treg cells to suppress the proliferation of effector T cells8,39. Furthermore, the rescue of Il2ra−/− and Il2rb−/− mice from disease observed after adoptive transfer of wild-type Treg cells suggested the existence of major mechanisms of Treg cell–mediated suppression that are independent of IL-2-deprivation6,7. However, the last studies left open the major question of whether IL-2 consumption by Treg cells is essential for the suppression of IL-2R-sufficient Teff cells, since IL-2 is probably a main driver of autoimmune disease in the absence of functional Treg cells.
A chief limiting factor in efforts to experimentally assess a role for IL-2R signaling in and IL-2 consumption by Treg cells in their function in vivo has been the lack of adequate genetic tools. We addressed this issue through the conditional deletion of Il2ra and Il2rb alleles and ablation of the expression of these genes in Treg cells in combination with induced expression of an active form of STAT5. These new genetic tools enabled us to unequivocally demonstrate a cell-intrinsic, essential role for IL-2R signaling not only in the maintenance of mature Treg cells and their fitness but also in their suppressor function. Furthermore, we found that STAT5 deficiency in Treg cells resulted in a similar loss of suppressor function and that expression of an active form of STAT5 rescued mice from the fatal disease that results from IL-2R deficiency. These results suggested a key role for IL-2R–STAT5 signaling in linking the differentiation and maintenance of Treg cells and their function. STAT5 binds to the Foxp3 promoter and the intronic Foxp3 regulatory element CNS2 and is involved in the induction and maintenance of Foxp3 expression38. Complexes of the transcription factors Runx and CBFβ also bind to CNS2 and the Foxp3 promoter and affect Foxp3 expression40. Although both CNS2-deficient Treg cells and CBFβ-deficient Treg cells do exhibit reduced Foxp3 expression resembling that of STAT5- or IL-2R-deficient Treg cells, the impairment of suppressor function in the last is much more severe. Thus, the decrease in Foxp3 expression alone could not account for the severe loss of Treg cell suppressor function in the absence of STAT5 or IL-2R. Indeed, our analysis of gene expression and functional features conferred by expression of the active form of STAT5 pointed to a heightened ability of Treg cells to bind to DCs and suppress their activation. Furthermore, expression of an active form of STAT5 partially 'rescues' the nearly complete loss of Treg cell suppressor function in the absence of TCR signaling34,35. Such results might appear to be at odds with the published finding that a transgene encoding STAT5b-CA driven by the proximal Lck promoter and Eμ enhancer fails to curtail fatal lymphoproliferative disease in Il2rb−/− mice despite restoring Foxp3 expression and Treg cell differentiation in the thymus9. However, the interpretation of the last result is problematic due to the massive population expansion of pre-leukemic T cells and B cells and reduced expression of the STAT5b-CA-encoding transgene in peripheral Treg cells.
Our studies have demonstrated that depriving Teff cells of IL-2 by Treg cells was fully dispensable for the suppression of IL-2R-sufficient CD4+ T cells, even though IL-2R signaling was required. However, IL-2R-dependent consumption of IL-2 by Treg cells was indispensable for the suppression of CD8+ T cell responses. The last, seemingly unexpected finding makes sense given the observed exquisite sensitivity of both naive CD8+ T cells and activated CD8+ T cells to IL-2-induced stimulation. Furthermore, IL-2 is produced upon activation of both naive CD4+ T cells and CD8+ T cells within hours of TCR engagement, in contrast to the production of effector cytokines such as IL-4 and IFN-γ, which requires the differentiation of naive T cells into Teff cells on a much longer time scale41. Such distinguishing features provide a likely explanation for the need for a distinct mechanism for the control of CD8+ T cell responses by Treg cells through IL-2 consumption.
It has been suggested that sensing of local IL-2 production by Treg cells enables 'licensing' of their suppressor function21. However, the 'rescue' of the suppression of CD4+ T cell responses by IL-2R-deficient Treg cells expressing an active form of STAT5 suggested that activated Treg cells can suppress autoimmunity without identifying the cellular source of IL-2. Thus, while IL-2 is a booster for the suppressor function of Treg cells, it might not have an indispensable role as a cue for specific targeting.
Genetically modified T cells are emerging as a potent means of therapy in some forms of cancer. The observed enhanced suppressor activity of Treg cells expressing an active form of STAT5 and significantly reduced severity of organ-specific autoimmunity in their presence would suggest that such modification of Treg cells might hold promise for the optimal design of Treg cell–based therapies for a variety of autoimmune and inflammatory disorders and organ transplantation.
Our findings have highlighted a central role for IL-2R-signaling-driven activation of STAT5 in supporting and boosting the suppressor function of differentiated Treg cells. In this context, it is noteworthy that although a Foxp3 ortholog has not been identified in birds, CD4+ T cell subsets with high expression of IL-2Rα have in vitro suppressor activity in chicken and ducks42,43. This suggests the importance of evolutionary conservation of IL-2Rα function in suppressive T cells.
Foxp3Cre and Foxp3Cre–ERT2 mice were described previously17,44. Il2rafl mice were generated by J.D.F. Stat5a/bfl mice were provided by L. Henninghausen. ApcMin mice were purchased from the Jackson Laboratory. The targeting strategies to generate Il2rbfl (generated by UK) and Rosa26Stat5bCA alleles are shown in Supplementary Figure 7. Tcrafl mice were described previously34. The experimental mice were either generated on or backcrossed onto a C57BL/6J (B6) background, bred and housed in the specific pathogen-free animal facility at Memorial Sloan Kettering Cancer Center. All animal experiments were approved by institutional animal care and use committee at Memorial Sloan Kettering Cancer Center and were performed in accordance with the institutional guidelines. For survival analysis, mice were monitored daily; unhealthy mice were euthanized once they were found lethargic and were counted as non-survivors. For tamoxifen treatment, tamoxifen (Sigma-Aldrich) was dissolved in olive oil at a concentration of 40 mg/ml. Mice were given oral gavage of 100 μl of tamoxifen emulsion per treatment. In experimental autoimmune encephalomyelitis and infection experiments, mice were challenged 2–3 months after a single gavage of tamoxifen and assessed as described previously38.
Flow cytometry and cell sorting.
Cells were stained with fluorescence-tagged antibodies purchased from eBioscience, BD Biosciences, Tonbo Bioscience or BioLegend (Supplementary Table 2) and analyzed using a BD LSR II flow cytometer. Flow cytometry data were analyzed using FlowJo software (TreeStar). For intracellular cytokine staining, cells were stimulated for 5 h with antibodies to CD3 and CD28 (5 μg/ml each) in the presence of brefeldin A or monensin, harvested and stained with eBioscience Fixation Permeabilization kit. For intracellular phosphorylated STAT5 staining, cells were stimulated with or without rmIL-2 for 20 min, fixed and permeabilized with 4% PFA followed by 90% methanol, and stained with anti-pY-STAT5 antibody (BD Biosciences). Cell sorting of Foxp3+ and Foxp3− cells was performed based on YFP or GFP expression using a BD FACSAria II cell sorter.
Listeria and vaccinia infection.
Mice were given intravenous injection of L. monocytogenes (LM10403S; 2000 cells/mouse) into the tail vein on day 0 and analyzed on day 8. For the detection of L. monocytogenes–specific immune responses, splenic DCs from unchallenged B6 mice sorted using CD11c microbeads (Miltenyi) were cultured in wells of a 96-well U-bottom plate (2 × 104 cells/well) with heat-killed L. monocytogenes (2 × 107 cells/well) for 6 h before the analysis. The cells were then co-cultured with splenic T cells obtained from L. monocytogenes–infected mice (1 × 105 cells/well) for 5 h in the presence of brefeldin A, and cytokine-producing T cells were detected by flow cytometry. For vaccinia virus infection, mice were given intravenous injection of non-replicating virus (5 × 107 PFU/mouse) on day 0 and analyzed on day 8. Splenocytes were re-stimulated with various vaccinia-virus-derived antigenic peptides (1 μg/ml) for 5 h in the presence of brefeldin A, and cytokine-producing T cells were detected by flow cytometry.
In vivo IL-2 neutralization.
Mice were given intraperitoneal injection of a cocktail of two different anti-IL-2 monoclonal antibodies, JES6-1 and S4B6-1 (BioXcell), or isotype-matched control antibody (rat IgG2a, 2A3; BioXcell), 200 μg each, twice a week, starting from 5–7 d after birth.
TAT-Cre treatment of T cells.
For the induction of STAT5b-CA expression in non-Treg cells, 1 × 107 CD4+Foxp3− or CD8+Foxp3− T cells sorted from the LNs and spleens of Foxp3Cre and Rosa26Stat5bCAFoxp3Cre mice were resuspended in 2 ml of serum-free RPMI medium containing a TAT-Cre recombinase (Millipore; 50 μg/ml) and incubated at 37 °C for 45 min. The cells were washed with RPMI containing 10% FCS, resuspended in PBS, and injected into T cell–deficient (Tcrb−/−Tcrd−/−) mice together with or without separately sorted Treg cells for in vivo suppression assay.
In vitro IL-2 capture assay.
Pooled cells from LNs and spleens were depleted of B cells and accessary cells by panning and T cells were enriched. The cells were stained with anti-CD8 and anti-B220 (Supplementary Table 2), and CD4+ Treg cells were sorted on the basis of GFP (YFP) expression alone in CD8-negative population. The sorted cells were divided among eight wells of a 96-well V-bottomed plate (2 × 105 cells/well) in 25 μl RPMI medium (10% FCS) with or without increasing doses of recombinant human IL-2 (0.016 to 12 U/ml), followed by incubation for 2 h at 37 °C. Depletion of IL-2 from the medium was assessed with the BD Cytometric Bead Array and Human IL-2 Enhanced Sensitivity Flex Set according to the manufacturer's instructions (BD Biosciences).
In vitro T cell–DC conjugation assay.
Treg cells and non-Treg cells were sorted in the same manner as in the IL-2 capture assay. Splenic CD11c+ DCs were isolated by magnetic-activated cell sorting from B6 mice given injection of Flt3L-secreting B16 melanoma cells. Treg and non-Treg cells were stained with CFSE. DCs were stained with CellTrace Violet (Molecular Probes). 1 × 104 Treg or non-Treg cells were cultured together with graded numbers of DCs (1 × 104 to 1 × 105) in a 96-well round-bottomed plate for 720 min in the presence or absence of rmIL-2 (100 IU/ml). Frequencies of Treg cells conjugated with DCs (% CTV+CFSE+/CFSE+) were analyzed by flow cytometry.
In vitro suppression assay.
Naive CD4+ T cells (responder cells) and Treg cells were purified by flow cytometry and stained with CellTrace Violet. 4 × 104 naive CD4+ T cells were cultured with graded numbers of Treg cells in the presence of 1 × 105 irradiated, T cell–depleted, CFSE-stained splenocytes and 1 μg/ml anti-CD3 (145-2C11, Bioxcell) in a 96-well round-bottom plate for 80 h. Cell proliferation of responder T cells and Treg cells (live CFSE−CD4+Foxp3− and Foxp3+) was determined by flow cytometry based on the dilution of fluorescence intensity of CellTrace Violet of the gated cells.
Measurement of serum and fecal immunoglobulin.
Serum IgM, IgG1, IgG2a, IgG2b, IgG2c, IgG3 and IgA were measured by ELISA using SBA Clonotyping System (Southern Biotech). IgE ELISA was performed using biotinylated anti-IgE (R35-118, BD Biosciences) and HRP-conjugated streptavidin. For measurement of fecal IgA, fresh fecal pellets were collected and dissolved in extraction buffer (7 μl per mg pellet) containing 50 mM Tris-HCl, 150 mM NaCl, 0.5% NP-40, 1mM EDTA, 1 mM DTT, and protease inhibitor cocktail (Complete mini; Roche). Supernatants were collected after centrifugation, titrated, and IgA was measured by ELISA.
Statistical analysis for animal experiments.
Each mouse was tagged with a unique identification number, and researchers were blinded to the genotypes of mice, except for adjustment of sample size included in a single experiment and after data analysis was completed. Wild-type mice with suspected congenital anomalies were excluded from the study. Cell samples that showed less than 70% cell vitality after preparation or after in vitro stimulation were excluded from the study. Statistical analyses were performed using Prism software with two-tailed unpaired Student's t-test. Welch's correction was applied when F-test was positive. P values of <0.05 were considered significant.
Male 8-week-old Rosa26Stat5bCAFoxp3Cre-ERT2 (STAT5b-CA) and Foxp3Cre–ERT2 (control) mice, nine mice for each experimental group, received a single dose (4 mg) of tamoxifen by oral gavage 4 months before isolation. Splenic CD4+Foxp3(YFP/GFP)+GITRhiCD25hi Treg and CD4+Foxp3(YFP/GFP)−CD62LhiCD44lo naive T cells were double sorted using a BD FACSAria II cell sorter, and a total of 12 samples were generated. Spleen T cell subsets isolated from three individual mice in the same experimental group were pooled into one biological replicate; three biological replicates were subjected to RNA-seq analysis for each experimental group. Total RNA was extracted and used for poly(A) selection and Illumina TruSeq paired-end library preparation following manufacturer's protocols. Samples were sequenced on the Illumina HiSeq 2500 to an average depth of 27.5 × 106 50-bp read pairs per sample. All samples were processed at a same time and sequenced on the same lane to avoid batch effects.
Read alignment and processing followed a method previously described45. Raw reads were trimmed using Trimmomatic v0.32 with standard settings to remove low-quality reads and adaptor contamination46. The trimmed reads were then aligned to the mouse genome (Ensembl assembly GRCm38) using TopHat2 v2.0.11 implementing Bowtie2 v2.2.2 with default settings. Read alignments were sorted with SAMtools v0.1.19 before being counted to genomic features using HTSeq v0.6.1p1. The overall read alignment rate across all samples was 74.5%. Differential gene expression was analyzed using DESeq2 1.6.3 in R (version 3.1.0)47.
Bioinformatics analysis of RNA-seq.
The distribution of read counts across all genes was bimodal. The assumption that this corresponded to 'expressed' and 'non-expressed' genes was supported by examination of marker genes known to be expressed or not expressed in Treg cells and naive T cells. The local minimum between the two peaks was chosen to be the threshold for expression. Using this threshold of ∼60 normalized reads, 10,589 of 39,179 genes were called as present. Genes significantly upregulated (342) or downregulated genes (314) in STAT5b-CA Treg cells relative to their expression in control Treg cells were defined as expressed genes with a change in expression of at least 1.5-fold or 0.67-fold, respectively, and a FDR-adjusted P value of ≤ 0.05.
'TCR-upregulated' (i.e., TCR-dependent) genes were defined as genes downregulated (a change in expression of at least 0.57-fold) in TCR-deficient relative to their expression inTCR-sufficient CD44hi Treg cells, while 'TCR-downregulated' genes were upregulated (at least 1.75-fold; Padj ≤ 0.001) in TCR-deficient CD44hi Treg cells (GSE61077)34. 'Activation-upregulated' genes were genes upregulated (twofold change; Padj ≤ 0.01) in Treg cells from Foxp3DTR mice recovering from transient depletion of Treg cells (GSE55753)33.
Signaling pathway impact analysis was performed using the R package of the same name48. Genes significantly up- and downregulated, and their changes in expression, were analyzed as one set for enrichment and perturbation of 90 Mus musculus KEGG (Kyoto Encyclopedia of Genes and Genomes) pathways accessed on 5 October 2015. The net pathway perturbation z-score was calculated using the observed net perturbation accumulation, and the mean and s.d. of the null distribution of net perturbation accumulations. Global P values were calculated using the normal inversion method with Bonferroni correction.
Biological-process (BP) gene-ontology (GO) term over-representation was calculated using BiNGO (v3.0.3)49 in Cytoscape v3.2.1, employing the hypergeometric test and applying a significance cutoff of FDR-adjusted P value of ≤0.05. The 10,589 expressed genes were entered as the reference set, and the GO ontology and annotation files used were downloaded on 25 October 2015 (Supplementary Table 1). The output from BiNGO was imported into EnrichmentMap (v2.0.1)50 in Cytoscape to cluster redundant GO terms and visualize the results. An EnrichmentMap was generated using a Jaccard similarity coefficient cutoff of 0.2, a P-value cutoff of 0.001, an FDR-adjusted cutoff of 0.005, and exclusion of gene sets with fewer than ten genes. The network was visualized using the default 'Prefuse Force-Directed Layout' in Cytoscape with default settings and 500 iterations. Groups of similar GO terms were manually circled.
GEO: microarray data, GSE84553.
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We thank T. Kitamura (The University of Tokyo) for the mSTAT5b-CA vector (pMX-STAT5B(1*6)); K. Rajewsky (Max Delbrück Center) for the Rosa26 construct; and L. Henninghausen (US National Institutes of Health) for Stat5a-Stat5bfl mice. Supported by the Japan Society for the Promotion of Science, Strategic Young Researcher Overseas Visits Program for Accelerating Brain Circulation (T.C.), Lucille Castori Center for Microbes, Inflammation & Cancer (T.C.), the US National Institutes of Health Medical Scientist Training Program (T32GM07739 to the Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program, for A.G.L. and X.F.), the US National Institutes of Health (P30 CA008748 to Memorial Sloan Kettering Cancer Center Core Facilities; and R37 AI034206 to A.Y.R.), DFG Emmy Noether programme (G.G.), the Ludwig Center at Memorial Sloan Kettering Cancer Center (A.Y.R.), Hilton-Ludwig Cancer Prevention Initiative funded by the Conrad N. Hilton Foundation and Ludwig Cancer Research (A.Y.R.), and the Howard Hughes Medical Institute (A.Y.R.).
A.K.K. and J.D.F. were employees of Biogen during the completion of this work; A.K.K. is an employee of AbbVie; and J.D.F. is an employee of Juno Therapeutics.
Integrated supplementary information
Supplementary Figure 1 IL-2R signaling is indispensable for the maintenance and function of Treg cells.
(a) The analysis shown in Fig. 1j performed by gating on CD62LhiCD44lo (upper panels) and CD62LloCD44hi (lower panels) YFP+Foxp3+ Treg cell subsets. (b) The expressions of CD62L and CD44 in CD3+CD4+Foxp3+ (upper panels) and frequencies of Foxp3+ cells among CD3+CD4+ cells (lower panels) in the spleen and small intestine lamina propria lymphocytes (SILPL) of the indicated mice (5 wk old). The right graph shows the summary data. (c) The expression of indicated markers by splenic CD3+CD4+Foxp3+ cells in the indicated mice (5 wk old). (d) Lifespan of Foxp3CreIl2rafl/fl (solid; n=25) and Foxp3CreIl2rafl/wt (dotted; n=20) mice. (e) Analysis of LN cellularity, Foxp3 expression levels (MFI) and frequencies of Foxp3+ Treg cells among CD3+CD4+ cells (upper panels) and pro-inflammatory cytokine production by CD4+Foxp3− and CD8+Foxp3− cells (lower panels) in the indicated mice (4 wk old). (f) Histopathology of the indicated organs of 4-wk-old Foxp3CreIl2rafl/fl mice. Scale bar, 100 μm. (g) The expression of Foxp3 and CD25 in LN CD4+ T cells in the indicated mice (6 wk old). The lower histogram represents the expression levels of CD25 in Foxp3+ cells shown in the upper panels. (h) The expression of CD62L and CD44 in LN CD3+CD4+Foxp3− (upper panels) and CD3+CD8+Foxp3− (lower panels) cells. (i, j) Cytokine production by splenic CD4+Foxp3− (i) and CD8+Foxp3− (j) cells isolated from indicated mice and in vitro stimulated with anti-CD3/CD28 for 5 hr. (k) Histopathology of the indicated organs of 4-wk-old Foxp3CreStat5a/bfl/fl mice. Scale bar, 100 μm. Sex and age matched mice were analyzed. Cells were analyzed by flow cytometry. *, P < 0.05; **, P < 0.01; ***, P < 0.001 (two-tailed unpaired Student’s t test). Data are from one experiment representative of three (a) or two (b, c, e) independent experiments with similar results with three or more mice per group in each experiment (a, b, c, e; each dot represents a single mouse; mean ± s.e.m.) or representative data of n=6 (b), n=3 (f), n=8 (g, h, i, j), n=5 (k) mice per group analyzed are shown.
Supplementary Figure 2 Restoration of the suppressor activity of IL-2Rα-deficient Treg cells by expression of an active form of STAT5.
(a) The schematic of Rosa26Stat5bCA allele. CAG, cytomegalovirus early enhancer element with the promoter, the first exon and the first intron of chicken beta-actin gene and the splice acceptor of the rabbit beta-globin gene; IRES, internal ribosome entry site; EGFP, enhanced green fluorescent protein (b, c) Photographs of 4-wk-old mice. (d) The expression of Foxp3 and CD25 in CD3+CD4+ cells in the LNs and spleens of the indicated mice (4 wk old). (e) Intracellular phospho-STAT5 levels in Treg cells from the indicated mice in vitro stimulated with rmIL-2 (1,000 U/ml) for 20 min. (f) The expression of CD62L and CD44 in CD3+CD4+Foxp3− and CD3+CD8+Foxp3− cells in the LNs of the indicated mice. (g) Cytokine production by splenic CD4+Foxp3− cells stimulated for 5 hr with anti-CD3/CD28. (h) The numbers of CD3+CD4+Foxp3−IFN-γ+ (left graph) and CD3+CD8+Foxp3−IFN-γ+ (right graph) cells in the LNs of the indicated mice (4 wk old). (i) The frequencies CD44hi cells among CD4+Foxp3− cells (upper left graph) and the frequencies of CD62LloCD44hi and CD62LhiCD44hi cells among CD8+Foxp3− cells (upper right graph) in the LNs of Foxp3CreIl2rafl/wt, Foxp3CreIl2rafl/wtRosa26Stat5bCA, Foxp3CreIl2rafl/fl, and Foxp3CreIl2rafl/flRosa26Stat5bCA mice at the indicated ages. Lower graphs show the numbers of each cell subset in the LNs of indicated mice. (j) Lifespan of Foxp3CreIl2rafl/fl (solid; n=25) and Foxp3CreIl2rafl/flRosa26Stat5bCA (dotted; n=21) mice. ***, P < 0.001 (two-tailed unpaired Student’s t test). Data are from one experiment representative of two (e, i) or three (h) independent experiments with similar results with three or more mice per group in each experiment (h, i; mean ± s.e.m.) or representative data of more than six mice per group analyzed are shown (d, f, g).
Supplementary Figure 3 Effects of in vivo neutralization of IL-2 on the activation of CD4+ or CD8+ cells.
(a) Representative flow cytometric analyses for the experiment shown in Fig. 2e. (b) LN cells of Foxp3Cre (upper 6 panels) and Foxp3CreIl2rbfl/fl (lower 8 panels) mice were unstimulated (US) or stimulated with rmIL-2 (1,000 or 10 U/ml) for 20 min, and intracellular levels of phospho-STAT5 in Treg (CD4+YFP+CD25hi), T naive (YFP−CD44loCD25lo; CD4+ and CD8+), and Teff (YFP−CD44hi; CD25lo and CD25hi; CD4+ and CD8+) cells were analyzed by flow cytometry. Data are representative of two independent experiments with three biological replicates in each experiment.
Supplementary Figure 4 Characterization of mice with Treg cells expressing an active form of STAT5.
(a) The frequencies of STAT5b-CA-expressing CD4+Foxp3+ cells among total CD4+Foxp3+ cells in the spleen of Foxp3Cre-ERT2Rosa26Stat5bCA mice after a single tamoxifen gavage on day 0. (b) The frequencies of STAT5b-CA-expressing CD4+Foxp3+ cells among total CD4+Foxp3+ cells in the indicated organs of Foxp3Cre-ERT2Rosa26Stat5bCA mice three months after a single tamoxifen gavage. (c) TCR Vβ usage of the Treg cells in various tissues 2 months after tamoxifen gavage. MLNs, mesenteric lymph nodes; PPs, Peyer’s patches. (d) Changes in body weights after tamoxifen gavage. 4-month-old Foxp3Cre-ERT2 (black, n=7) and Foxp3Cre-ERT2Rosa26Stat5bCA (blue, n=7) mice were gavaged with tamoxifen and body weights were monitored the following 4 months. (e) Serum chemistry profiles 4.5 months after tamoxifen gavage. (f–h) General characterization of Treg cells of Foxp3Cre-ERT2 (black) and Foxp3Cre-ERT2Rosa26Stat5bCA (blue) mice three months after a single tamoxifen gavage. (f) The expression levels of indicated molecules on CD4+Foxp3+ cells in the indicated organs. (g) The frequencies of Foxp3+ cells among CD3+CD4+ cells (upper graph) and the expression levels of Foxp3 in the CD3+CD4+Foxp3+ cells (lower graph) in the indicated organs. (h) The frequencies of Foxp3+ cells among CD3+CD8+ cells in the indicated organs. (i) In vitro suppressor activity of Treg cells. Treg cells were isolated from Foxp3Cre-ERT2 (control) and Foxp3Cre-ERT2Rosa26Stat5bCA (STAT5b-CA) mice and co-cultured with T naive cells (responder cells). The proliferative activities of Treg and responder cells were determined by flow cytometry based on the dilution of CellTrace Violet (CTV) fluorescence intensity. Typical dye dilution patterns of T naive cells at a 4:1 responder vs. Treg cell ratio are shown in the left two panels. Summary graphs showing the proliferation of co-cultured responder T cells (Foxp3−) and Treg cells (Foxp3+) are shown in the right two panels. CTV MFI of cells inversely correlates with cell division. Cells were analyzed by flow cytometry (a–c, f–i). *, P < 0.05; **, P < 0.01; ***, P < 0.001 (two-tailed unpaired Student’s t test). Data are from one experiment representative of two (c, d, i) or three or more (a, b, f–h) independent experiments with similar results with three or more biological replicates per group in each experiment. Each dot represents a single mouse (b, e–h). mean ± s.e.m. (a, b, d–i).
Supplementary Figure 5 Systemic reduction in the Teff cell population in the presence of STAT5b-CA+ Treg cells.
(a–d) Analysis of Foxp3Cre-ERT2 (black dots) and Foxp3Cre-ERT2Rosa26Stat5bCA (blue dots) mice three months after a single tamoxifen treatment. (a, b) The frequencies of Ki-67+ (upper graphs), CD62LhiCD44lo (middle; % T naive), and CD62LloCD44hi (lower; % Teff) cells among CD4+Foxp3− (a) and CD8+Foxp3− (b) cells of the indicated organs. (c) Cytokine production by CD4+Foxp3− cells in the spleen and mesenteric LN cells stimulated with anti-CD3/CD28 for 5 hr. (d) Serum Ig levels determined by ELISA. (e) The numbers and sizes of polyps in the distal small intestines of 5-month-old Foxp3Cre-ERT2ApcMin/+ and Foxp3Cre-ERT2Rosa26Stat5bCAApcMin/+ mice treated with tamoxifen at 4 wk of age. Cells were analyzed by flow cytometry (a–c). *, P < 0.05; **, P < 0.01; ***, P < 0.001 (two-tailed unpaired Student’s t test). Data are from one experiment representative of three or more independent experiments with similar results with three or more mice per group in each experiment (a–c) or pooled samples with n=10 or more were analyzed (d, e). Each dot represents a single mouse (a–e). mean ± s.e.m. (a–e).
Supplementary Figure 6 RNA-seq analysis (supplementary information for Fig. 5)
(a) Plot of gene expression (as log2 normalized read count) in control T naive versus STAT5b-CA T naive cells (i.e., naive CD4+ T cells from Foxp3Cre-ERT2Rosa26Stat5bCA mice). The diagonal lines indicate fold change of at least 1.5× or 0.67× fold. Significantly up- and down-regulated genes (defined as genes with at least 1.5× or 0.67× fold change, adjusted P-value ≤ 0.05, and expression above a minimal threshold based on the distribution of all genes) are colored red or blue, respectively, and their numbers are shown. (b) Volcano plot showing log10 FDR-adjusted P-values versus log2 fold change between STAT5b-CA and control Treg cells. Genes that fall outside of the x- or y-axis range of this plot are shown on the axes as empty triangles. The vertical and horizontal gray lines indicate 1.5× or 0.67× fold change (±log2 1.5 = ±0.58) and P = 0.05 (−log10 0.05 = 1.3), respectively. (c) Network analysis of GO term enrichment among significantly downregulated genes in STAT5b-CA expressing vs. control Treg cells. Downregulated genes were analyzed for over-represented GO terms using BiNGO in Cytoscape, and the resulting network was calculated and visualized using EnrichmentMap. Groups of similar GO terms were manually circled. Edge thickness and color are proportional to the similarity coefficient between connected gene sets. Node color is proportional to the FDR-adjusted P-value of the enrichment. Node size is proportional to gene set size.
Supplementary Figure 7 Strategies for targeting Il2rbfl and Rosa26Stat5bCA alleles.
(a) Generation of a conditional Il2rb allele and Il2rb targeting strategy. The targeting vector was constructed such that upon Cre-mediated deletion, the promoter region and exon 2 which comprises the first ATG of Il2rb were deleted with simultaneous activation of eGFP expression. Shown from top to bottom i) the Il2rb locus with the promoter region, exons and translational start site in exon 2 (E2); ii) the targeting vector comprising an eGFP, a triple SV40 polyA site (tpA), a PGK neopA cassette, a PGK promoter (Pr.) downstream of exon 2, a TK gene, and loxP and frt sites; arrows denote the orientation; iii) the targeted Il2rb locus. Restriction sites, probes used for detection and the expected fragments detected by Southern blot analysis are indicated. Correctly targeted embryonic stem (ES) cell lines were identified by Southern blot analysis of XbaI-digested DNA that displayed the 4.0 kb band of the integrated transgene along with the 14.0 kb wild-type band. Co-integration of the 3’ loxP site was verified by PCR analysis using primers that hybridize in a unique region spanning the PGK promoter and the 3’ frt site (forward primer) and in a region upstream of intron 3 of Il2rb (reverse primer). (b) The schematic of, and targeting strategy for Rosa26Stat5bCA allele. The targeting vector was constructed such that CAG promoter driven STAT5b-CA is expressed upon Cre-mediated deletion of a STOP cassette. Correctly targeted ES cell lines were identified by Southern blot analysis of EcoRI-digested DNA that displayed the 5.9 kb (probe A; 5’ side) and 11.6 kb (probe F; 3’ side) bands of the integrated transgene along with the 15.6 kb wild-type band (probe A and F; both sides).
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Chinen, T., Kannan, A., Levine, A. et al. An essential role for the IL-2 receptor in Treg cell function. Nat Immunol 17, 1322–1333 (2016). https://doi.org/10.1038/ni.3540
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