胸腺基质淋巴细胞生成素
先天性淋巴细胞
生物
间质细胞
免疫学
细胞生物学
间充质干细胞
利基
免疫
炎症
免疫系统
癌症研究
生态学
作者
Madelene W. Dahlgren,Stephen W. Jones,Kelly M. Cautivo,Alexandra Dubinin,Jorge F. Ortiz-Carpena,Sepideh Farhat,Kevin Shengyang Yu,Katharine Lee,Chaoqun Wang,Anna V. Molofsky,Aaron D. Tward,Matthew F. Krummel,Tien Peng,Ari B. Molofsky
出处
期刊:Immunity
[Cell Press]
日期:2019-02-26
卷期号:50 (3): 707-722.e6
被引量:320
标识
DOI:10.1016/j.immuni.2019.02.002
摘要
Type 2 lymphocytes promote both physiologic tissue remodeling and allergic pathology, yet their physical tissue niches are poorly described. Here, we used quantitative imaging to define the tissue niches of group 2 innate lymphoid cells (ILC2s), which are critical instigators of type 2 immunity. We identified a dominant adventitial niche around lung bronchi and larger vessels in multiple tissues, where ILC2s localized with subsets of dendritic and regulatory T cells. However, ILC2s were most intimately associated with adventitial stromal cells (ASCs), a mesenchymal fibroblast-like subset that expresses interleukin-33 (IL-33) and thymic stromal lymphopoietin (TSLP). In vitro, ASCs produced TSLP that supported ILC2 accumulation and activation. ILC2s and IL-13 drove reciprocal ASC expansion and IL-33 expression. During helminth infection, ASC depletion impaired lung ILC2 and Th2 cell accumulation and function, which are in part dependent on ASC-derived IL-33. These data indicate that adventitial niches are conserved sites where ASCs regulate type 2 lymphocyte expansion and function.
科研通智能强力驱动
Strongly Powered by AbleSci AI