体内
FOXP3型
转化生长因子
体外
生物
功能(生物学)
化学
调节器
免疫学
细胞生物学
免疫系统
基因
生物化学
遗传学
作者
Yang Luo,Youqiu Xue,Julie Wang,Junlong Dang,Qiannan Fang,Gonghua Huang,Nancy J. Olsen,Song Guo Zheng
出处
期刊:Cell Reports
[Elsevier]
日期:2019-02-01
卷期号:26 (7): 1869-1879.e3
被引量:59
标识
DOI:10.1016/j.celrep.2019.01.066
摘要
High-salt diets inhibit the suppressive function of thymus-derived natural regulatory T cells (tTreg). Transforming growth factor β (TGF-β)-induced ex vivo regulatory T cells (iTreg) comprise another Treg subset that exhibits similarities and differences with tTreg. Here, we demonstrate that iTregs are completely stable and fully functional under high salt conditions. High salt does not influence the development, differentiation, and functional activities of iTreg but affects Foxp3 stability and function of tTreg in vitro and in vivo. In addition, high salt does not significantly change the transcription profiles of the iTreg signature or pro-inflammatory genes. Therefore, we conclude that iTreg, unlike tTreg, are stable and functional in the presence of high salt. Our findings provide additional evidence that iTreg may have different biological features from tTreg and suggest a greater potential for clinical utility in patients with autoimmune diseases, in which the complicated role of environmental factors, including diet, must be considered.
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