蛋白激酶C
免疫突触
肿瘤坏死因子α
效应器
细胞生物学
T细胞
封锁
功能(生物学)
受体
免疫学
细胞因子
炎症
生物
激酶
T细胞受体
癌症研究
生物化学
免疫系统
作者
Alexandra Zanin‐Zhorov,Yi Ding,Sudha Kumari,Mukundan Attur,Keli L. Hippen,Maryanne L. Brown,Bruce R. Blazar,Steven B. Abramson,Juan J. Lafaille,Michael L. Dustin
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2010-03-26
卷期号:328 (5976): 372-376
被引量:278
标识
DOI:10.1126/science.1186068
摘要
T cell receptor (TCR)-dependent regulatory T cell (Treg) activity controls effector T cell (Teff) function and is inhibited by the inflammatory cytokine tumor necrosis factor-alpha (TNF-alpha). Protein kinase C-theta (PKC-theta) recruitment to the immunological synapse is required for full Teff activation. In contrast, PKC-theta was sequestered away from the Treg immunological synapse. Furthermore, PKC-theta blockade enhanced Treg function, demonstrating PKC-theta inhibits Treg-mediated suppression. Inhibition of PKC-theta protected Treg from inactivation by TNF-alpha, restored activity of defective Treg from rheumatoid arthritis patients, and enhanced protection of mice from inflammatory colitis. Treg freed of PKC-theta-mediated inhibition can function in the presence of inflammatory cytokines and thus have therapeutic potential in control of inflammatory diseases.
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