共 29 条
Identification and distribution of developing innate lymphoid cells in the fetal mouse intestine
被引:139
作者:

Bando, Jennifer K.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Med, San Francisco, CA USA Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA

Liang, Hong-Erh
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h-index: 0
机构:
Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Med, San Francisco, CA USA
Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA USA Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA

Locksley, Richard M.
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h-index: 0
机构:
Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Med, San Francisco, CA USA
Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA USA Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
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.
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页码:153 / +
页数:10
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