Retinoic acid regulates the development of a gut-homing precursor for intestinal dendritic cells

被引:75
|
作者
Zeng, R. [1 ,2 ]
Oderup, C. [1 ,2 ]
Yuan, R. [1 ,2 ]
Lee, M. [1 ,2 ]
Habtezion, A. [3 ]
Hadeiba, H. [1 ,2 ]
Butcher, E. C. [1 ,2 ]
机构
[1] Stanford Univ, Dept Pathol, Sch Med, Lab Immunol & Vasc Biol, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Ctr Mol Biol & Med, Palo Alto, CA USA
[3] Stanford Univ, Dept Med Gastroenterol, Sch Med, Stanford, CA 94305 USA
关键词
T-CELLS; ALDEHYDE DEHYDROGENASE; IN-VIVO; DIFFERENTIATION; SPECIFICITY; INHIBITION; MONOCYTES; LYMPH;
D O I
10.1038/mi.2012.123
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The vitamin A metabolite retinoic acid (RA) regulates intestinal immune responses through immunomodulatory actions on intestinal dendritic cells (DCs) and lymphocytes. Here, we show that RA also controls the generation of gut-tropic migratory DC precursors, referred to as pre-mucosal DCs (pre-mu DCs). Pre-mu DCs express the gut trafficking receptor alpha 4 beta 7 and home preferentially to the intestines. They develop in the bone marrow (BM), can differentiate into CCR9(+) plasmacytoid DCs as well as conventional DCs (cDCs), but preferentially give rise to CD103(+) intestinal cDCs. Generation of pre-mu DCs in vivo in the BM or in vitro is regulated by RA and RA receptor alpha (RAR alpha) signaling. The frequency of pre-mu DCs is reduced in vitamin A-deficient animals and in animals treated with RAR inhibitors. The results define a novel vitamin A-dependent, RA-regulated developmental sequence for DCs and identify a targeted precursor for CD103(+) cDCs in the gut.
引用
收藏
页码:847 / 856
页数:10
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