Essential Role for Retinoic Acid in the Promotion of CD4+ T Cell Effector Responses via Retinoic Acid Receptor Alpha

被引:311
|
作者
Hall, Jason A. [1 ,5 ]
Cannons, Jennifer L. [2 ]
Grainger, John R. [1 ]
Dos Santos, Liliane M. [1 ]
Hand, Timothy W. [1 ]
Naik, Shruti [1 ,5 ]
Wohlfert, Elizabeth A. [1 ]
Chou, David B. [1 ]
Oldenhove, Guillaume [1 ]
Robinson, Melody [3 ]
Grigg, Michael E. [4 ]
Kastenmayer, Robin [3 ]
Schwartzberg, Pamela L. [2 ]
Belkaid, Yasmine [1 ]
机构
[1] NIAID, Mucosal Immun Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[2] NHGRI, Genet Dis Res Branch, NIH, Bethesda, MD 20892 USA
[3] NIAID, Comparat Med Branch, NIH, Bethesda, MD 20892 USA
[4] NIAID, Mol Parasitol Unit, NIH, Bethesda, MD 20892 USA
[5] Univ Penn, Immunol Grad Grp, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
VITAMIN-A-DEFICIENCY; DENDRITIC CELLS; TOXOPLASMA-GONDII; SIGNALING PATHWAY; SMALL-INTESTINE; TH17; CELLS; FOXP3; DIFFERENTIATION; MICE; METABOLISM;
D O I
10.1016/j.immuni.2011.03.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vitamin A and its metabolite, retinoic acid (RA) are implicated in the regulation of immune homeostasis via the peripheral induction of regulatory T cells. Here we showed RA was also required to elicit proinflammatory CD4(+) helper T cell responses to infection and mucosal vaccination. Retinoic acid receptor alpha (RAR alpha) was the critical mediator of these effects. Antagonism of RAR signaling and deficiency in RAR alpha (Rara(-/-)) resulted in a cell-autonomous CD4(+) T cell activation defect, which impaired intermediate signaling events, including calcium mobilization. Altogether, these findings reveal a fundamental role for the RA-RAR alpha axis in the development of both regulatory and inflammatory arms of adaptive immunity and establish nutritional status as a broad regulator of adaptive T cell responses.
引用
收藏
页码:435 / 447
页数:13
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