| First Author | Zhang X | Year | 2018 |
| Journal | Cell Rep | Volume | 24 |
| Issue | 3 | Pages | 607-618 |
| PubMed ID | 30021159 | Mgi Jnum | J:270822 |
| Mgi Id | MGI:6278764 | Doi | 10.1016/j.celrep.2018.06.052 |
| Citation | Zhang X, et al. (2018) OX40 Costimulation Inhibits Foxp3 Expression and Treg Induction via BATF3-Dependent and Independent Mechanisms. Cell Rep 24(3):607-618 |
| abstractText | Naive CD4(+) T cells can be converted to Foxp3(+) T regulatory cells (Tregs) in the periphery (iTregs), where induction of Foxp3 gene expression is central to Treg differentiation. OX40 signaling is known to inhibit Foxp3 expression and Treg induction, but the underlying mechanisms remain poorly defined. Here, we found that OX40 costimulation activates two distinct molecular pathways to suppress Foxp3 expression in freshly activated naive CD4(+) T cells. Specifically, OX40 upregulates BATF3 and BATF, which produce a closed chromatin configuration to repress Foxp3 expression in a Sirt1/7-dependent manner. Moreover, OX40 can also activate the AKT-mTOR pathway, especially in the absence of BATF3 and BATF, to inhibit Foxp3 induction, and this is mediated by phosphorylation and nuclear exclusion of the transcription factor Foxo1. Taken together, our results provide key mechanistic insights into how OX40 inhibits Foxp3 expression and Treg induction in the periphery. |
