Identification and distribution of developing innate lymphoid cells in the fetal mouse intestine

被引:139
作者
Bando, Jennifer K. [1 ,2 ]
Liang, Hong-Erh [1 ,2 ,3 ]
Locksley, Richard M. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[3] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
ROR-GAMMA-T; TISSUE INDUCER CELLS; PEYERS-PATCHES; ORGANOGENESIS; LYMPHOTOXIN; DIFFERENTIATION; EXPRESSION; DEFICIENT; CYTOKINES; RESPONSES;
D O I
10.1038/ni.3057
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fetal lymphoid tissue inducer (LTi) cells are required for lymph node and Peyer's patch (PP) organogenesis, but where these specialized group 3 innate lymphoid cells (ILC3s) develop remains unclear. Here, we identify extrahepatic arginase-1(+) Id2(+) fetal ILC precursors that express a transitional developmental phenotype (ftILCPs) and differentiate into ILC1s, ILC2s and ILC3s in vitro. These cells populate the intestine by embryonic day (E) 13.5 and, before PP organogenesis (E14.5-15), are broadly dispersed in the proximal gut, correlating with regions where PPs first develop. At E16.5, after PP development begins, ftILCPs accumulate at PP anlagen in a lymphotoxin-alpha-dependent manner. Thus, ftILCPs reside in the intestine during PP development, where they aggregate at PP anlagen after stromal cell activation and become a localized source of ILC populations.
引用
收藏
页码:153 / +
页数:10
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