T细胞受体
刺激
细胞骨架
原子力显微镜
悬臂梁
肌动蛋白
生物物理学
T细胞
抗原
显微镜
化学
肌动蛋白细胞骨架
免疫突触
细胞生物学
受体
细胞
材料科学
纳米技术
生物
物理
免疫学
生物化学
免疫系统
神经科学
光学
复合材料
作者
Kenneth H. Hu,Manish J. Butte
标识
DOI:10.1083/jcb.201511053
摘要
Triggering of the T cell receptor (TCR) integrates both binding kinetics and mechanical forces. To understand the contribution of the T cell cytoskeleton to these forces, we triggered T cells using a novel application of atomic force microscopy (AFM). We presented antigenic stimulation using the AFM cantilever while simultaneously imaging with optical microscopy and measuring forces on the cantilever. T cells respond forcefully to antigen after calcium flux. All forces and calcium responses were abrogated upon treatment with an F-actin inhibitor. When we emulated the forces of the T cell using the AFM cantilever, even these actin-inhibited T cells became activated. Purely mechanical stimulation was not sufficient; the exogenous forces had to couple through the TCR. These studies suggest a mechanical–chemical feedback loop in which TCR-triggered T cells generate forceful contacts with antigen-presenting cells to improve access to antigen.
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