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CORRESPONDENCE Jinfang Zhu: jfzhu{at}niaid.nih.gov
 Top ABSTRACT RESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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Upon T cell activation, naive CD4+ T cells can differentiate into distinct cell lineages, including the classical Th1 and Th2 cells (1, 2), as well as the recently defined Th cells producing IL-17 (Th17 cells) (3) and inducible Treg (iTreg) cells (4). These cells play important roles in adaptive immunity (5). Th1 cells mainly produce IFN-
The cytokine milieu during CD4 T cell activation is one of the most important factors in determining T cell fate. IL-12 and IFN-
Growth factor independent 1 (Gfi-1), a transcriptional repressor, was initially reported as a protooncogene that allows an IL-2–dependent cell line to be IL-2 independent (32). Gfi-1 was also found as a common insertion site in Moloney murine leukemia virus–induced T lymphomas (33, 34). During Th2 cell differentiation, the expression levels of GATA-3 are enhanced as a result of TCR-mediated signaling and/or activation of the IL-4–Stat6 pathway (35, 36). In collaboration with Stat5, activated by IL-2, GATA-3 induces remodeling of the Il4 locus and the capacity to produce IL-4 when cells are stimulated through TCRs. Gfi-1 is transiently induced by TCR stimulation (37, 38). Its expression is further enhanced and prolonged by IL-4, resulting in optimal Th2 cell proliferation (37). Gfi-1 selects GATA-3hi cells to grow in IL-2, suggesting that there is a selective component involving Gfi-1 in Th2 cell differentiation (37).
Three groups, including ours, have generated germline Gfi1 KO mice (39–41). Many abnormalities have been observed, including neutropenia (39, 40), a T cell development defect (41, 42), a hematopoietic stem cell defect (43, 44), and defects in dendritic cell development and function (45). The profound defect in T cell development in Gfi1–/– mice is associated with a large proportion of their peripheral CD4 T cells displaying memory-like phenotypes (40), presumably as a result of lymphopenia-driven cell proliferation and differentiation.
To analyze the role played by Gfi-1 in the differentiation and/or growth of normal CD4 T cells, we generated Gfi1 conditional KO (Gfi1 cKO) mice (41) in which Gfi-1 is deleted only in T cells. Th2 cells differentiated from Gfi1 cKO mice have a severe defect in cell expansion. In vivo, the Th2 response is dramatically impaired in these KO mice. On the other hand, IFN-
and are involved in immunity against intracellular pathogens. Th2 cells produce IL-4, IL-5, and IL-13, are involved in immunity against helminths and other extracellular parasites, and enhance antibody responses. Th17 cells produce IL-17a, IL-17f, IL-21, and IL-22, and are critical for immunity against extracellular bacteria and fungi. Th1, Th2, and Th17 cells are also involved in the induction or maintenance of autoimmune and immunopathologic diseases. Thus, Th1 and Th17 cells are linked to many organ-specific autoimmune diseases, and Th2 cells play critical roles in asthma and other allergic diseases. iTreg cells, functionally similar to naturally occurring Treg cells (6), can regulate immune responses. Among naturally occurring Treg cells, a subset expressing CD103 has been reported to contain the highest suppressive activity and to be present in the mucosal tissues, such as in the gut, as well as at sites of inflammation (7, 8). Interestingly, a large number of CD4 cells differentiated in the presence of TGF-β in vitro express CD103 (9), and TGF-β has been shown to induce Treg cell differentiation (4). induce Th1 cell differentiation (10–12); IL-4 and IL-2 induce Th2 cell differentiation (13–16), TGF-β and IL-6/IL-21 induce Th17 cell differentiation (17–19), and TGF-β and IL-2 induce iTreg cell generation (4, 20). Although several transcription factors are involved in the differentiation and maintenance of each Th cell type, Th cell differentiation is mainly controlled by specific master transcription factors and Stat family members: T-bet and Stat4 for Th1 cells (21–23), GATA-3 and Stat5 for Th2 cells (14, 24–27), RORt and Stat3 for Th17 cells (28, 29), and Foxp3 and Stat5 for Treg cells (4, 20, 30, 31). production is enhanced in the absence of Gfi-1, raising the possibility that Gfi-1 may negatively regulate the differentiation of other Th cell lineages. We report that Gfi-1 suppresses both Th17 and CD103+ iTreg cell differentiation, whereas TGF-β, critical for Th17 and iTreg cell induction, down-regulates Gfi-1 expression. In the absence of Gfi-1, Foxp3+CD103+ Treg cells are preferentially expanded in vivo upon immunization.
RESULTS
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ABSTRACT
RESULTS
DISCUSSION
MATERIALS AND METHODS
REFERENCES
Th2 cells lacking Gfi1 display an active genomic configuration at the Cd103, Rorc, and Il23r loci
Th2 cells differentiated from Gfi1 cKO (Gfi1fl/fl-CD4Cre) mice have a severe defect in cell expansion and also produce some IFN-, suggesting that Gfi-1 is important for sustaining the Th2 cell phenotype. A recent report suggests that Gfi-1, as a transcriptional repressor, is associated with the histone lysine-specific demethylase 1 (LSD1), which results in demethylation of histone 3 lysine 4 (H3K4) at target promoters (46). LSD1 demethylates mono- and dimethylation but not trimethylation of H3K4. However, because of the balance of different methylation states, active gene promoter regions usually contain higher levels of H3K4 trimethylation than of mono- and dimethylation (47). To search for Gfi-1 target genes in T cells, the chromatin immunoprecipitation (ChIP)–Seq technology was applied. We used H3K4 trimethylation, the end product of H3K4 methylation, as an indicator, reasoning that such modification would not accumulate in Gfi1–/– cells at Gfi-1 target sites because of a lack of the mono- or dimethylated forms of H3K4. As expected, both wild-type and Gfi1 cKO Th2 cells displayed a similar pattern of H3K4 trimethylation at the Gata3 locus (Fig. 1 A).1 Because H3K4 methylation is associated with active chromatin, this indicates that Gfi-1, although important for Th2 expansion, is not essential for the Th2 polarization process. Interestingly, at the Cd103 locus, whose expression is associated with a subset of Treg cells, Gfi1 cKO Th2 cells showed high levels of H3K4 modification that was absent in wild-type Th2 or Th17 cells (Fig. 1 B). At the Rorc locus, which encodes RORt, critical for Th17 cell differentiation, Gfi1 cKO Th2 cells displayed levels of H3K4 modification similar to Th17 cells (Fig. 1 C). H3K4 modification was also detected at the Il23r locus in Gfi1 cKO Th2 cells (Fig. 1 D). Such a modification was absent in wild-type Th2 cells. Gfi1 cKO Th2 cells did not appear to be contaminated with Th17 cells, because H3K4 trimethylation at the Il21 and Il17f loci was not observed the Gfi1 cKO Th2 cells, although it was prominent in Th17 cells (Fig. 1, E and F). These results indicate that Gfi-1 plays an important role in chromatin remodeling of Th17 and iTreg cell–related genes, including Rorc, Il23r, and Cd103, in Th2 cells. Although Gfi1 cKO Th2 cells displayed an active Rorc locus, expression of RORt in Gfi1 cKO Th2 cells is much lower than that in Th17 cells (unpublished data), indicating that additional factors, possibly induced by TGF-β and IL-6, are required for Rorc expression as well as for the induction of IL-17.
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IL-4 has been reported to suppress the induction of IL-17 production (49, 50). The detailed mechanism is not clear. To test whether Gfi-1 mediates the suppression of IL-17 by IL-4, we performed a Th17 to Th2 switching experiment. Indeed, IL-4 suppressed IL-17 production (from 3.7 to 0.5%) and induced IL-4 production (from 0.1 to 6.4%) in wild-type cells (Fig. 2 C), but IL-4 failed to suppress IL-17 production in Gfi1 cKO cells even though it still induced its own production. Gfi1 cKO cells showed an approximately twofold decrease in cell expansion, compared with wild-type cells, when switched from Th17 to Th2 conditions. Strikingly, 
1% of the cells can produce both IL-17 and IL-4 when Gfi1 cKO Th17 cells were switched to Th2 conditions, suggesting that Gfi-1 plays an important role in IL-4–mediated suppression of IL-17 production.
Gfi-1 expression is down-regulated by TGF-β
Because Gfi-1, induced by IL-4, has an effect on both RORt and IL-17, we tested the normal expression levels of Gfi-1 during Th17 cell differentiation. Gfi-1 expression was assessed by quantitative PCR after naive CD4 T cells were primed under Th1, Th2, Th17, and iTreg cell conditions for 4 d. As expected, cells primed under different conditions specifically expressed their hallmark genes (IFN- for Th1 cells, IL-4 for Th2 cells, IL-17a for Th17 cells, and Foxp3 for iTreg cells; Fig. 3 A). Th2 cells expressed approximately twice as much Gfi-1 as Th1 cells, as previously reported (37). Th17 and iTreg cells expressed very low levels of Gfi-1. To test when the difference in Gfi-1 expression occurred during the differentiation process, cells were harvested at various time points after priming under different conditions. As early as 24 h after stimulation, Gfi-1 was strikingly underexpressed in cells primed under Th17 and iTreg cell conditions (Fig. 3 B).
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Expression of Gfi-1 inhibits IL-17 production but not induction of RORt in cells primed with TGF-β plus IL-6
To test the importance of Gfi-1 down-regulation by TGF-β, Gfi-1 was introduced by retroviral infection into activated CD4 T cells primed under Th17 conditions. 4 d after infection, IL-17 production was assessed upon restimulation with PMA plus ionomycin. A similar proportion of the cells infected by control GFP–retroviral vector (RV) and uninfected cells, in the same culture, produced IL-17 (17.8 vs. 15%; Fig. 4 A, left). However, only 3.9% of the cells infected by the Gfi-1–GFP-RV, compared with 14.1% of the uninfected cells in the same culture, produced IL-17. Three independent experiments showed significant suppression of IL-17 production by Gfi-1 (Fig. 4 A, right).
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t has been reported to be the master regulator for Th17 cells and TGF-β plus IL-6 are required for Th17 cell differentiation (17–19, 28), we tested the expression of RORt, TGF-βRs, and IL-6R
among Th1, Th2, and Th17 cells. RORt was selectively expressed in Th17 cells, consistent with previous reports (Fig. S1 A, available at http://www.jem.org/cgi/content/full/jem.20081666/DC1). Interestingly, both TGF-βRI and TGF-βRII were expressed at higher levels in Th17 cells than in Th1 and Th2 cells. IL-6R was also found to be highest in Th17 cells (Fig. S1 A). 3 d after infection with Gfi-1–GFP-RV, although expression of RORt, TGF-βRI, and TGF-βRII in infected cells was not affected (Fig. 4 B and Fig. S1 B), expression of IL-6R was suppressed (Fig. S1 B). Consistent with the intracellular staining results shown in Fig. 4 A, both IL-17a and IL-17f mRNA levels were reduced by enforced expression of Gfi-1 (Fig. 4 B). Enforced Gfi-1 expression in Gfi1 cKO Th17 cells also suppressed IL-17a but not RORt expression (Fig. S2). Suppression of IL-17 requires the Gfi-1 suppressive domain, because Gfi-1 bearing a single mutation in this domain (Gfi-1(P2A)) failed to suppress IL-17 production (Fig. 4 C).
The failure of Gfi-1 to suppress RORt transcription in this setting is apparently at odds with the genomic data shown in Fig. 1, in which the Rorc locus is not H3K4 trimethylated in wild-type Th2 cells but is trimethylated in Gfi1 cKO Th2 cells. However, this discrepancy may be explained by the fact that retroviral-mediated expression of Gfi-1 does not occur until 24–48 h after infection, whereas RORt up-regulation by TGF-β occurred within 24 h (unpublished data). Alternatively, Gfi-1 may require another Th2 factor as a cosuppressor of RORt transcription. Nevertheless, the data indicate that Gfi-1 suppresses IL-17 even when RORt is normally expressed.
To test the direct binding of Gfi-1 to its putative target genes, ChIP using anti–Gfi-1 antibody was performed. The Gfi-1 DNA binding sites contain AATC, and sequences containing AAATCNNNG are represented at the highest frequency in a random oligonucleotide selection assay, suggesting that such sequences may have particularly high binding affinity for Gfi-1 (51). Eight putative Gfi-1 binding sites containing AAATCNNNG or its complement CNNNGATTT, including the Rorc promoter (Rorcp) from the Rorc locus and nine sites from the Il17a/Il17f loci along with Gfi1 promoter (Gfi1p) as a positive control (52), were tested for Gfi-1 binding. Only the Gfi1p region near the GAAAATCGAAGTA sequence and an intergenic region of Il17a/Il17f near the AGAAATCTCAGGG sequence but not the other sites tested were enriched by the anti–Gfi-1 antibody in this assay (Fig. 4 D, left). Consistent with Gfi-1 binding, this Il17a/Il17f intergenic region also recruited LSD1 in wild-type cells, and the binding of LSD1 to this site was not found in the absence of Gfi-1 (Fig. 4 D, right).
When CD4 T cells from Gfi1 cKO mice were primed under Th17 conditions, a higher percentage of the Gfi1 cKO cells than of wild-type cells produced IL-17 (28.4 vs. 14.5%, Fig. 4 E, left). In a series of nine independent experiments, there was a highly statistically significant increase in IL-17–producing cells among Gfi1 cKO Th17 cells compared with wild-type Th17 cells (Fig. 4 E, right). These data indicate that endogenous expression of Gfi-1 in Th17 cells, even at low levels, is sufficient to modulate IL-17 production. Indeed, because Gfi-1 can be induced transiently by TCR stimulation even in Th17 cells (unpublished data), such induction may serve as a negative regulator of IL-17 production.
Gfi-1 limits TGF-β–mediated differentiation of iTreg cells in vitro
Because Gfi-1 is also underexpressed in iTreg cells, we tested the effect of enforcing Gfi-1 expression during iTreg cell differentiation. Cells primed under iTreg cell conditions were infected with Gfi-1–GFP-RV or control GFP-RV. 4 d after infection, cells were costained for Foxp3 and IL-2 to identify bona fide Treg cells. In the group infected with control GFP-RV, the majority of both the GFP– and GFP+ cells were Foxp3+IL-2– (53.7 and 61.7%; Fig. 5 A). Although 69.2% of GFP– cells from the Gfi-1–GFP-RV–infected group were Foxp3+IL-2–, only 34.9% of GFP+ cells were Foxp3+IL-2–. Thus, enforced expression of Gfi-1 significantly reduced the generation of iTreg cells. Gfi-1 had a minimal effect on the frequency of Foxp3+ cells induced by TGF-β, but among the Foxp3+ cells, a higher percentage of cells also produced IL-2. In a separate experiment, enforced Gfi-1 expression during iTreg cell differentiation enhanced the proportion of IL-2–producing cells from 20 to 35%, whereas Gfi-1(P2A) had no effect (Fig. 5 B), suggesting that the repressive domain of the Gfi-1 is required for its function in regulating iTreg cell generation.
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20% of the Foxp3+ cells in wild-type mice were CD103+, whereas in Gfi1 cKO mice, such CD103+ cells represented 50% of the Foxp3+ Treg cells (Fig. 5 D, bottom). Three putative Gfi-1 binding sites containing AAATCACAG from the Cd103 locus were tested for Gfi-1 binding. The site from Cd103 intron 1 (near the GGAAATCACAGAG sequence), but not the other two sites, was enriched by Gfi-1 antibody by 15–20-fold (Fig. 5 E, left). LSD1 was also recruited to this site in wild-type but not Gfi-1 cKO cells (Fig. 5 E, right). These data suggest that CD103 is a direct target of Gfi-1.
Gfi-1 limits the expansion of Foxp3+CD103+ cells in vivo
To address the physiological effects of Gfi-1 on TGF-β–mediated responses in vivo, we studied the responses of the cKO mice and normal controls to MOG-induced experimental allergic encephalitis (EAE). As expected, 13–14 d after MOG immunization, wild-type mice began to develop clinical symptoms, with a peak in intensity at 3 wk. The onset of disease in Gfi1 cKO mice was significantly delayed, by approximately 1 wk (Fig. 6 A). IL-17 has been reported as a key player in the induction of the disease (53). IL-17a mRNA in CD4 T cells was measured by real-time PCR before or after various times of immunization without in vitro restimulation. There was an approximately twofold increase of IL-17a mRNA in Gfi1 cKO mice at all time points after MOG immunization (Fig. 6 B). Neither IFN- nor IL-4 mRNA was found to be consistently different from the levels in wild-type mice, possibly because of the modest Th1 or Th2 responses of these mice to immunization. CD103 mRNA is higher in Gfi1 cKO CD4 cells before immunization, consistent with the staining data shown in Fig. 5 D, and was further increased after MOG immunization. Ex vivo restimulation of CD4 T cells 1 wk after immunization followed by anti–IL-17 intracellular staining confirmed the enhancement of IL-17 production in Gfi1 cKO mice (Fig. 6 C). However, intracellular staining of IL-17–producing cells 3 wk after immunization revealed no difference between wild-type and Gfi1 cKO CD4 T cells (unpublished data). The discrepancy between IL-17 mRNA and IL-17 protein at 3 wk after immunization may result from the very strong stimulus used for restimulation. Nevertheless, the data certainly indicate that there was no defect in the generation and expansion of Th17 cells in Gfi1 cKO mice. Flow cytometry analysis showed a continuous increase of Foxp3+ cells in Gfi1 cKO mice after immunization, which peaked at 3 wk (39.1 and 38.5% in Gfi1 cKO mice compared with 22.8 and 20.5% in wild-type mice; Fig. 6 D). Although CD103+ Treg cells were already high in Gfi1 cKO mice before immunization, there was a substantial increase of such cells after immunization (26.1 and 28.9% in Gfi1 cKO mice vs. 6% and 3.7% in wild-type mice), suggesting that Gfi-1 normally plays a negative role in the expansion of Treg cells in vivo. No apparent lymphocyte infiltration into the central nervous system (CNS) was found in healthy mice from either group after immunization. However, among the sick mice, Foxp3+ cells were more abundant in the CNS of the Gfi1 cKO mice than of the wild-type mice (Fig. S3 A, available at http://www.jem.org/cgi/content/full/jem.20081666/DC1). Most Foxp3+ cells in the CNS were also CD103+ (Fig. S3 B). Thus, Foxp3+CD103+ Treg cells appear to have a dominant effect over the IL-17–producing cells in Gfi1 cKO mice resulting in the delay of disease onset.
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TopABSTRACTRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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than WT Th1 cells. In addition, Gfi1 cKO Th2 cells display a different pattern of chromatin histone modification than wild-type Th2 cells. These observations led us to reassess the function of Gfi-1 during T cell differentiation, particularly because two new Th lineages, Th17 and iTreg cells, have been recently defined. In this paper, we showed that Gfi-1 is down-regulated by TGF-β stimulation during Th17 and iTreg cell–inducing conditions, and enforced expression of Gfi-1 inhibits both Th17 and iTreg cell differentiation. Furthermore, in the absence of Gfi-1, the percentage of Foxp3+ cells that express CD103 was substantially higher than in wild-type mice, and this subset expanded in vivo upon immunization. Gfi-1 is a transcriptional repressor (51). Gfi-1 and its congener Gfi-1b have been recently reported to associate with the histone demethylase LSD1 and CoREST to form a repressive complex (46). Gfi-1 directs the complex to the promoter of target genes where LSD1 can demethylate H3K4 residues and thus repress transcription. Knockdown of LSD1 in erythroid cells leads to increased H3K4 dimethylation and trimethylation of Gfi-1b targets. In this paper, we showed that Il17a/Il17f and Cd103 are the targets for Gfi-1 in T cells. Furthermore, LSD1 is recruited to those sites in a Gfi-1–dependent manner.
The Rorc and Il23r promoter regions are heavily methylated on H3K4 residues in Gfi1 cKO Th2 cells but not in WT Th2 cells; methylation levels are comparable to those found in WT Th17 cells. However, we were not able to locate Gfi-1 binding sites within the Rorc or Il23r loci, suggesting that they may not be the direct targets of Gfi-1. A future goal will be to understand the mechanism through which Gfi-1 regulates the chromatin modification at the Rorc and Il23r loci. RORt is also expressed in the cells cultured under iTreg cell–inducing conditions, correlating with the H3K4 methylation in such cells, although iTreg cells fail to express IL-17 (unpublished data). These results indicate that RORt can be up-regulated by TGF-β alone (28) and that down-regulation of Gfi-1 by TGF-β is critical for RORt expression during Th17 cell differentiation.
In a model of EAE involving immunization with MOG, the percentage of IL-17–producing cells found in Gfi1 cKO mice was modestly higher than in wild-type controls. In addition, Toxoplasma gondii infection or Schistosoma mansoni egg injection induced higher levels of IL-17 production in Gfi1 cKO than in wild-type mice (unpublished data). Thus, similar to our in vitro results, the optimal appearance of IL-17–producing cells induced by TGF-β in vivo requires down-regulation of Gfi-1 expression, which is transiently induced by T cell activation and/or IL-4 stimulation.
Gfi-1 expression is also down-regulated by TGF-β during iTreg cell differentiation, and enforced expression of Gfi-1 partially suppresses the induction of Foxp3+IL-2– Treg cells. By down-regulating Gfi-1, Treg cells become more active and also display a tissue-seeking phenotype. In Gfi1 cKO mice, the proportion of Foxp3+CD103+ effector/memory Treg cells is already high, but this population is further increased after MOG immunization. In addition, Foxp3+CD103+ are also expanded during T. gondii infection or in response to S. mansoni egg injection (Fig. S4, available at http://www.jem.org/cgi/content/full/jem.20081666/DC1). We have not yet determined whether the increased percentage of Foxp3+CD103+ cells in the Gfi1 cKO mice and the expansion of this subset after immunization reflects a unique role for Gfi-1 in the development of Foxp3+CD103+ thymic-derived Foxp3+ T cells, or whether the higher percentage of Foxp3+CD103+ T cells is secondary to an increased contribution of peripherally generated Foxp3+CD103+ in the cKO mice that is further potentiated after immunization. In normal mice, the Foxp3+CD103+ cell population is actively cycling and contains a high proportion of apoptotic cells (7), so it remains possible that Gfi-1 may play a role in the homeostasis of this subset.
A selective effect of Gfi-1 on Treg cells with a modest effect on Th17 cell differentiation in vivo could be explained by the differential requirement of TGF-β in the induction of these two lineages. A low concentration of TGF-β is sufficient for Th17 cell differentiation, whereas iTreg cell differentiation requires a higher concentration of TGF-β (54). In the absence of Gfi-1, Treg cell numbers may increase in response to levels of TGF-β that normally only induce Th17 cell differentiation in wild-type mice after MOG immunization.
The selective expansion of the Foxp3+CD103+ cells correlates with delayed EAE onset. Treg cells have been suggested to suppress autoimmune diseases by several mechanisms: by suppressing the activation and expansion of the effector cells (6); by suppressing functions of effector cells, such as cytokine production (55); and by limiting recruitment of effector cells to sites of inflammation (56). In our model, the disease onset was delayed in the Gfi1 cKO mice, yet the number of effector cells that are capable of making IL-17 was not only not reduced but was modestly increased. Thus, it is most likely that the Foxp3+CD103+ cells suppress disease by affecting recruitment and/or activation of the effector cells at inflammation sites consistent with the tissue-seeking phenotype of the Foxp3+CD103+ T cells that are increased in frequency in Gfi1 cKO mice. The majority of Treg cells found in the CNS are Foxp3+CD103+, even in wild-type mice. In addition, Treg cells are a much larger proportion of CNS CD4 T cells in Gfi1 cKO than in wild-type mice.
Given the dual effects of Gfi-1 on effector and Treg cells, modulation of its expression and function could have opposite effects depending on the timing, location, and cell type in which it is expressed, just as is the case with the administration of TGF-β or anti–TGF-β (57). However, blockade of Gfi-1 function during early stages of autoimmune diseases may be beneficial through the resultant expansion of Treg cells. Likewise, the specific targeting of Gfi-1 in Treg cells may enhance their migration to sites of inflammation as well as increase their suppressive activity. Thus, the predominant effect of Gfi-1 on Treg cells in vivo suggests Gfi-1 and its pathway of action could be considered as a target for modulating Treg cells.
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MATERIALS AND METHODS |
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TopABSTRACTRESULTSDISCUSSIONMATERIALS AND METHODSREFERENCES |
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Cell culture.
Lymph node CD4 or CD8 T cells were prepared by MACS purification using CD4 or CD8 microbeads (Miltenyi Biotec), and purity was usually 90–95%. In some experiments, lymph node nonregulatory naive CD4 T cells were prepared by depleting CD8, B220, IAb, CD24, NK1.1, CD16/CD32, CD11b, and CD25-positive cells using FITC-labeled antibodies (BD), followed by anti-FITC microbeads and autoMACS purification (Miltenyi Biotec). T cell–depleted APCs were prepared by incubating spleen cells with anti-Thy1.2 and rabbit complement (Cedarlane Laboratories Limited) at 37°C for 45 min, and then irradiating them at 30 Gy (3,000 rad). T cells were co-cultured with APCs at a 1:5 ratio in the presence of 1 µg/ml anti-CD3 and 3 µg/ml anti-CD28, together with different combinations of antibodies and cytokines: for Th1 conditions, 10 µg/ml anti–IL-4, 10 ng/ml IL-12, and 100 U/ml IL-2; for Th2 conditions, 10 µg/ml anti–IFN- and 10 µg/ml anti–IL-12, 5,000 U/ml IL-4, and 100 U/ml IL-2; for Th17 conditions, 10 µg/ml anti–IL-4, 10 µg/ml anti–IFN-, 10 µg/ml anti–IL-12, 5 ng/ml TGF-β, 10 ng/ml IL-6, and 10 ng/ml IL-1β; for iTreg cell conditions, 10 µg/ml anti–IL-4, 10 µg/ml anti–IFN-, 10 µg/ml anti–IL-12, 5 ng/ml TGF-β, and 100 U/ml IL-2; for ThN (nonpolarization) conditions, 10 µg/ml anti–IL-4, 10 µg/ml anti–IFN-, 10 µg/ml anti–IL-12, and 100 U/ml IL-2; and for neutral conditions, no exogenous cytokines or antibodies were added.
Quantitative RT-PCR.
Total RNA was isolated using TRIzol (Invitrogen). First-strand cDNAs were made using the SuperScript Preamplification System (Invitrogen). Quantitative real-time PCR was performed on a sequence detection system (model 7900HT; Applied Biosystems). The sequences of the primers and minor groove binder (MGB) probe for Gfi-1 are 5'-TGGGCGGCGGCTCCTACAAAT-3', 5'-TGCGGTGTGGAGAACACCTGA-3', and FAM-5'-TGCAGCAAGGTGTT-3'-MGB, respectively. Inventoried primer/probe sets for detecting IFN- (Mm99999071_m1), IL-4 (4312482), IL-17a (Mm00439619_m1), IL-17f (Mm00521423_m1), Foxp3 (Mm00475156_m1), Bcl-2 (Mm00477631_m1), Bim (Mm00437795_m1), SOCS-1 (Mm00782550_s1), CD103 (Mm00434443_m1), CD4 (Mm00442754_m1), TGF-βRI (Mm00436971_m1), TGF-βRII (Mm00436978_m1), IL-6R (Mm00439653_m1), GAPDH (4308313), and RORt (Mm01261022_m1) were purchased from Applied Biosystems.
Preparation of retroviral constructs and infection.
Gfi-1–GFP-RV and Gfi-1(P2A)–GFP-RV were previously constructed (37). Retroviruses were packaged in the Phoenix-Eco packaging cell line, as previously described (36). Infection was performed at 24 h after the initiation of the culture in which CD4 T cells were activated with anti-CD3/anti-CD28 under neutral conditions in the presence of APCs.
Flow cytometry analysis.
The expression of GFP in retrovirally infected cells was measured by flow cytometry. Cell-surface staining was performed in PBS containing 0.1% PBS with different combination of antibodies. Anti–IFN-–FITC, anti–IL-4–PE, anti–IL-17a–PE, anti-CD25–PE, anti-CD25–PerCP–Cy5.5, anti-CD4–PE–Cy5, anti–IFN-–allophycocyanin, and anti-CD44–allophycocyanin were purchased from BD. Anti-CD103–FITC (2E7), anti-CD103–PE (2E7), anti-Foxp3–PE (FJK-16s), anti-Foxp3–allophycocyanin (FJK-16s), anti–IL-17a–Alexa Fluor 647 (eBio17B7), anti–IL-2–Pacific blue (JES6-5H4), anti-CD62L–Pacific blue (MEL-14), anti–IFN-–PerCP–Cy5.5 (XMG1.2), anti-CD44–allophycocyanin–Alexa Fluor 750 (IM7), and anti-CD4–Alexa Fluor 700 (GK1.5) were purchased from eBioscience. For intracellular cytokine staining, cells were restimulated with 10 ng/ml PMA and 1 µM ionomycin for 4 h or with platebound anti-CD3 and anti-CD28 (3 µg/ml each) for 6 h in the presence of 2 µM monensin during last 3 h. Harvested samples were fixed with 4% formaldehyde, washed, and permeabilized in 0.5% Triton X-100–0.1% BSA in PBS before staining for cytokine production. Intracellular staining of Foxp3 was performed according to the instructions of the Foxp3 staining kit (eBiosciences). When GFP is present, Foxp3 was stained in Triton X-100 buffer, which is used for staining cytokines.
ChIP and histone H3K4 modification analysis.
For Gfi-1 and LSD1 ChIP, 5 x 106 CD4+ T cells that have been cultured under Th2 or Th17 conditions for 4–5 d were cross-linked with formaldehyde treatment, and the chromatin was sonicated into small fragments from 200 to 1,000 bp. The fragmented chromatin was immunoprecipitated with the specific antibody. Anti–Gfi-1 (N-20) was purchased from Santa Cruz Biotechnology, Inc. Anti-LSD1 was purchased from Abcam. Precipitated DNA fragments were reverse cross-linked, and the enrichment of specific sites was tested by real-time PCR using SYBR green and the relative enrichment was normalized to a negative site from Gata3-intron3. The primers are as follows: Rorcp, 5'-ATTCCATGAGGGCTTGCCT-3' and 5'-ACCTGTCATCAGCCTCCCATA-3'; Gfi1p, 5'-CGAAGTATTCTTGGCTCCTGGA-3' and 5'-GCCCAAACAGTCGACAGGATT-3'; Il17a/Il17f, 5'-TGCTGGGCAGGAAGATACTC-3' and 5'-TCCCCACTCTGTCTTTCCAG-3'; Cd103-5', 5'-CCCACCCGCTGTAGACATGT-3' and 5'-CCCAGCCATACCCGAAGAT-3'; Cd103-intron1, 5'-CCCACCCAACACGTCCTCTAA-3' and 5'-CTCATATCTTAATCTAAGCACTCAGCGTT-3'; Cd103-3', 5'-CCCTGCCTGGACTACAAAGTG-3' and 5'-CTGCCTCCACCTCCCAAGT-3'; and Gata3-intron3, 5'-TCAGGGCACTAAGGGTTGTTAACTT-3' and 5'-GAATTCCATCCATGAGACACACAA-3'.
For ChIP-Seq experiments (47), 107 CD4+ T cells that have been cultured under Th2 or Th17 conditions for 4 d were cross-linked with formaldehyde treatment and digested with MNase to generate mainly mononucleosomes with a minor fraction of dinucleosomes. ChIP was performed by using anti-H3K4me3 (Abcam). The ChIP DNA ends were repaired using polynucleotide kinase and Klenow enzyme, followed by treatment with Taq polymerase to generate a protruding 3' A base used for adaptor ligation. After ligation of a pair of Solexa adaptors to the repaired ends, the ChIP DNA was amplified using the adaptor primers for 17 cycles, and the fragments around 220 bp (mononucleosome plus adaptors) were isolated from agarose gel. The purified DNA was used directly for cluster generation and sequencing analysis using the Illumina/Solexa 1G Genome Analyzer according to the manufacturer's protocols. Sequence reads were obtained and mapped to the mouse genome with the Illumina GA Pipeline. Read positions were adjusted 75 bp to be centered on the sequenced chromatin fragments, and the number of adjusted reads originating in 200-bp windows were summed and displayed as custom tracks on the University of California Santa Cruz Genome Browser.
EAE induction.
EAE was induced via subcutaneous immunization into the hind flank with 200 µl of an emulsion containing 400 µg of MOG35-55 peptide (MEVGWYRSPFSRVVHLYRNGK) and 400 µg of Mycobacterium tuberculosis strain H37Ra in complete Freund's adjuvant (Difco). On days 0 and 2, the mice received an intraperitoneal injection of 200 ng pertussis toxin (EMD) dissolved in PBS. Clinical symptoms were assessed by the following criteria: 0, no signs of disease; 1, complete tail paralysis; 2, hind limb paresis; 3, complete hind limb paralysis; 4, unilateral forelimb paralysis; and 5, moribund/death. Mice observed in a moribund state were killed. Data presented are the mean clinical scores of five mice per group.
Online supplemental material.
Fig. S1 shows the expression of RORt, TGF-βRI, TGF-RβRII, and IL-6R in Th1, Th2, and Th17 cells and in Gfi-1–RV–infected Th17 cells. Fig. S2 shows the suppression of IL-17 expression by Gfi-1 in Gfi1 cKO Th17 cells. Fig. S3 shows the frequency and the phenotype of Treg cells found in the CNS of the WT and Gfi1 cKO mice after MOG immunization. Fig. S4 shows the expansion of Foxp3+CD103+ Treg cells in Gfi1 cKO mice during T. gondii infection or in response to S. mansoni egg injection. Online supplemental material is available at http://www.jem.org/cgi/content/full/jem.20081666/DC1.
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Acknowledgments |
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This work is supported by the Division of Intramural Research, NIAID and the Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health.
The authors have no conflicting financial interests.
Submitted: 29 July 2008
Accepted: 12 January 2009
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