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胎鼠肠道中发育中的固有淋巴细胞的鉴定与分布

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

作者信息

Bando Jennifer K, Liang Hong-Erh, Locksley Richard M

机构信息

Departments of Microbiology and Immunology and Medicine, University of California, San Francisco, California, USA.

1] Departments of Microbiology and Immunology and Medicine, University of California, San Francisco, California, USA. [2] Howard Hughes Medical Institute, University of California, San Francisco, California, USA.

出版信息

Nat Immunol. 2015 Feb;16(2):153-60. doi: 10.1038/ni.3057. Epub 2014 Dec 15.

Abstract

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-α-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.

摘要

胎儿淋巴组织诱导细胞(LTi)对于淋巴结和派尔集合淋巴结(PP)的器官发生是必需的,但这些特殊的3型固有淋巴细胞(ILC3)的发育位置仍不清楚。在这里,我们鉴定出肝外精氨酸酶-1(+)Id2(+)胎儿ILC前体,它们表达一种过渡性发育表型(ftILCP),并在体外分化为ILC1、ILC2和ILC3。这些细胞在胚胎第13.5天(E13.5)时定位于肠道,并且在PP器官发生之前(E14.5 - 15)广泛分布于近端肠道,这与PP最初发育的区域相关。在E16.5,PP发育开始后,ftILCP以淋巴毒素-α依赖的方式在PP原基处聚集。因此,ftILCP在PP发育期间存在于肠道中,在基质细胞激活后它们在PP原基处聚集,并成为ILC群体的局部来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d93/4297560/650167324a47/nihms643351f1.jpg

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