Short-chain fatty acids induce both effector and regulatory T cells by suppression of histone deacetylases and regulation of the mTOR-S6K pathway

被引:974
作者
Park, J. [1 ]
Kim, M. [1 ]
Kang, S. G. [1 ]
Jannasch, A. H. [2 ]
Cooper, B. [2 ]
Patterson, J. [3 ]
Kim, C. H. [1 ,4 ,5 ]
机构
[1] Dept Comparat Pathobiol, Lab Immunol & Hematopoiesis, W Lafayette, IN 47907 USA
[2] Bindley Biosci Ctr, Metabolite Profiling Facil, W Lafayette, IN USA
[3] Purdue Univ, Dept Anim Sci, W Lafayette, IN 47907 USA
[4] Weldon Sch Biomed Engn, W Lafayette, IN USA
[5] Purdue Univ, Purdue Ctr Canc Res, W Lafayette, IN 47907 USA
关键词
GUT MICROBIOTA; INFLAMMATORY RESPONSES; MAMMALIAN TARGET; TH17; CELLS; DIFFERENTIATION; ROLES; EXPRESSION; BUTYRATE; GPR43; METABOLITES;
D O I
10.1038/mi.2014.44
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Microbial metabolites, such as short-chain fatty acids (SCFAs), are highly produced in the intestine and potentially regulate the immune system. We studied the function of SCFAs in the regulation of T-cell differentiation into effector and regulatory Tcells. We report that SCFAs can directly promote T-cell differentiation into Tcells producing interleukin-17 (IL-17), interferon-gamma and/or IL-10 depending on cytokine milieu. This effect of SCFAs on Tcells is independent of GPR41 or GPR43, but dependent on direct histone deacetylase (HDAC) inhibitor activity. Inhibition of HDACs in Tcells by SCFAs increased the acetylation of p70 S6 kinase and phosphorylation rS6, regulating the mTOR pathway required for generation of Th17 (T helper type 17), Th1, and IL-10(+) Tcells. Acetate (C2) administration enhanced the induction of Th1 and Th17 cells during Citrobacter rodentium infection, but decreased anti-CD3-induced inflammation in an IL-10-dependent manner. Our results indicate that SCFAs promote T-cell differentiation into both effector and regulatory Tcells to promote either immunity or immune tolerance depending on immunological milieu.
引用
收藏
页码:80 / 93
页数:14
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