瑞士/瑞士法郎
染色质重塑
细胞生物学
染色质
转录因子
炎症
生物
癌症研究
免疫学
遗传学
基因
作者
Xiaoqian Liu,Kuai Liu,Yuxi Wang,Xiaoyu Meng,Qianqian Wang,Sijue Tao,Qianying Xu,Xin Shen,Xianzhi Gao,Shenghui Hong,Huihui Jin,James Q. Wang,Di Wang,Linrong Lu,Zhuo-Xian Meng,Lie Wang
出处
期刊:Cell Reports
[Cell Press]
日期:2024-07-01
卷期号:43 (7): 114458-114458
被引量:5
标识
DOI:10.1016/j.celrep.2024.114458
摘要
Regulatory T (Treg) cells play a critical regulatory role in the immune system by suppressing excessive immune responses and maintaining immune balance. The effective migration of Treg cells is crucial for controlling the development and progression of inflammatory diseases. However, the mechanisms responsible for directing Treg cells into the inflammatory tissue remain incompletely elucidated. In this study, we identified BAF60b, a subunit of switch/sucrose nonfermentable (SWI/SNF) chromatin remodeling complexes, as a positive regulator of Treg cell migration that inhibits the progression of inflammation in experimental autoimmune encephalomyelitis (EAE) and colitis animal models. Mechanistically, transcriptome and genome-wide chromatin-landscaped analyses demonstrated that BAF60b interacts with the transcription factor RUNX1 to promote the expression of CCR9 on Treg cells, which in turn affects their ability to migrate to inflammatory tissues. Our work provides insights into the essential role of BAF60b in regulating Treg cell migration and its impact on inflammatory diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI