TRPV1型
促炎细胞因子
T细胞
细胞生物学
T细胞受体
化学
免疫突触
炎症
瞬时受体电位通道
受体
生物
免疫学
生物化学
免疫系统
作者
Samuel Bertin,Yukari Aoki‐Nonaka,Petrus R. de Jong,Lilian L. Nohara,Hongjian Xu,Shawna R. Stanwood,Sonal Srikanth,Jihyung Lee,Keith To,Lior Abramson,Timothy Z. Yu,Tiffany Han,Ranim Touma,Xiangli Li,José M. González‐Navajas,Scott Herdman,Maripat Corr,Guo Fu,Hui Dong,Yousang Gwack
出处
期刊:Nature Immunology
[Nature Portfolio]
日期:2014-10-05
卷期号:15 (11): 1055-1063
被引量:230
摘要
TRPV1 is a Ca(2+)-permeable channel studied mostly as a pain receptor in sensory neurons. However, its role in other cell types is poorly understood. Here we found that TRPV1 was functionally expressed in CD4(+) T cells, where it acted as a non-store-operated Ca(2+) channel and contributed to T cell antigen receptor (TCR)-induced Ca(2+) influx, TCR signaling and T cell activation. In models of T cell-mediated colitis, TRPV1 promoted colitogenic T cell responses and intestinal inflammation. Furthermore, genetic and pharmacological inhibition of TRPV1 in human CD4(+) T cells recapitulated the phenotype of mouse Trpv1(-/-) CD4(+) T cells. Our findings suggest that inhibition of TRPV1 could represent a new therapeutic strategy for restraining proinflammatory T cell responses.
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