ATF4
效应器
平衡
生物
转录因子
细胞生物学
免疫学
未折叠蛋白反应
内质网
基因
遗传学
作者
Ke Wang,Andrea Farrell,Enchen Zhou,Houji Qin,Zixuan Zeng,Kailun Zhou,Karina Cunha e Rocha,Dinghong Zhang,Gaowei Wang,Amha Atakilit,Dean Sheppard,Li‐Fan Lu,Chunyu Jin,Wei Ying
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2025-03-14
卷期号:10 (105): eadp7193-eadp7193
被引量:9
标识
DOI:10.1126/sciimmunol.adp7193
摘要
Regulatory T cells (Tregs) have diverse functional specification in homeostasis and disease. However, how liver Tregs function and are transcriptionally regulated in obesity is not well understood. Here, we identified that effector Tregs expressing activating transcription factor 4 (ATF4) were enriched in the livers of obese mice. ATF4 was critical for driving an effector Treg transcriptional program, and ATF4-expressing Tregs promoted the development of obesity-induced liver fibrosis by enhancing transforming growth factor-β activation via integrin αvβ8. Treg-specific deletion of Atf4 resulted in reduced liver Tregs and attenuation of obesity-induced liver abnormalities. Furthermore, ATF4 was required to promote the differentiation of nonlymphoid tissue Treg precursors under steady state. These findings demonstrate that ATF4 is important for regulating Treg functional specification in homeostasis and obesity.
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