Cytoskeletal forces during signaling activation in Jurkat T-cells

被引:122
|
作者
Hui, King Lam [1 ]
Balagopalan, Lakshmi [3 ]
Samelson, Lawrence E. [3 ]
Upadhyaya, Arpita [1 ,2 ]
机构
[1] Univ Maryland, Dept Phys, College Pk, MD 20742 USA
[2] Univ Maryland, Inst Phys Sci & Technol, College Pk, MD 20742 USA
[3] NCI, Cellular & Mol Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
MYOSIN-II FUNCTION; IMMUNOLOGICAL SYNAPSE; TRACTION FORCES; ARP2/3; COMPLEX; RECEPTOR MICROCLUSTERS; ACTIN CYTOSKELETON; RETROGRADE FLOW; SUBSTRATE; RIGIDITY; MOTILITY;
D O I
10.1091/mbc.E14-03-0830
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
T-cells are critical for the adaptive immune response in the body. The binding of the T-cell receptor (TCR) with antigen on the surface of antigen-presenting cells leads to cell spreading and signaling activation. The underlying mechanism of signaling activation is not completely understood. Although cytoskeletal forces have been implicated in this process, the contribution of different cytoskeletal components and their spatial organization are unknown. Here we use traction force microscopy to measure the forces exerted by Jurkat T-cells during TCR activation. Perturbation experiments reveal that these forces are largely due to actin assembly and dynamics, with myosin contractility contributing to the development of force but not its maintenance. We find that Jurkat T-cells are mechanosensitive, with cytoskeletal forces and signaling dynamics both sensitive to the stiffness of the substrate. Our results delineate the cytoskeletal contributions to interfacial forces exerted by T-cells during activation.
引用
收藏
页码:685 / 695
页数:11
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