Transcription Factor KLF10 Constrains IL-17-Committed V?4+ ?? T Cells.

ABSTRACT: ?? T cells, known to be an important source of innate IL-17 in mice, provide critical contributions to host immune responses. Development and function of ?? T cells are directed by networks of diverse transcription factors (TFs). Here, we examine the role of the zinc finger TFs, Kruppel-like factor 10 (KLF10), in the regulation of IL-17-committed CD27- ?? T (??27--17) cells. We found selective augmentation of V?4+ ??27- cells with higher IL-17 production in KLF10-deficient mice. Surprisingly, KLF10-deficient CD127hi V?4+ ??27--17 cells expressed higher levels of CD5 than their wild-type counterparts, with hyper-responsiveness to cytokine, but not T-cell receptor, stimuli. Thymic maturation of V?4+ ??27- cells was enhanced in newborn mice deficient in KLF10. Finally, a mixed bone marrow chimera study indicates that intrinsic KLF10 signaling is requisite to limit V?4+ ??27--17 cells. Collectively, these findings demonstrate that KLF10 regulates thymic development of V?4+ ??27- cells and their peripheral homeostasis at steady state.

SUBMITTER: Kim G 

PROVIDER: S-EPMC5835516 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature