生物
RAR相关孤儿受体γ
细胞生物学
再生(生物学)
肠道菌群
平衡
炎症
免疫学
干细胞
细胞分化
细胞
免疫系统
FOXP3型
遗传学
基因
作者
Bola S. Hanna,Gang Wang,Silvia Galván-Peña,Alexander O. Mann,Ricardo N. Ramírez,Andrés R. Muñoz-Rojas,Kathleen M. Smith,Min Wan,Christophe Benoist,Diane Mathis
出处
期刊:Immunity
[Elsevier]
日期:2023-04-01
卷期号:56 (4): 829-846.e8
被引量:42
标识
DOI:10.1016/j.immuni.2023.01.033
摘要
Specific microbial signals induce the differentiation of a distinct pool of RORγ+ regulatory T (Treg) cells crucial for intestinal homeostasis. We discovered highly analogous populations of microbiota-dependent Treg cells that promoted tissue regeneration at extra-gut sites, notably acutely injured skeletal muscle and fatty liver. Inflammatory meditators elicited by tissue damage combined with MHC-class-II-dependent T cell activation to drive the accumulation of gut-derived RORγ+ Treg cells in injured muscle, wherein they regulated the dynamics and tenor of early inflammation and helped balance the proliferation vs. differentiation of local stem cells. Reining in IL-17A-producing T cells was a major mechanism underlying the rheostatic functions of RORγ+ Treg cells in compromised tissues. Our findings highlight the importance of gut-trained Treg cell emissaries in controlling the response to sterile injury of non-mucosal tissues.
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