Traction stress in focal adhesions correlates biphasically with actin retrograde flow speed

被引:360
作者
Gardel, Margaret L. [1 ]
Sabass, Benedikt [2 ,3 ,4 ]
Ji, Lin [5 ]
Danuser, Gaudenz [5 ]
Schwarz, Ulrich S. [2 ,3 ,4 ]
Waterman, Clare M. [6 ]
机构
[1] Univ Chicago, Dept Phys, Chicago, IL 60637 USA
[2] Univ Heidelberg, BIOQUANT, D-69120 Heidelberg, Germany
[3] Univ Karlsruhe, Inst Zool, D-76131 Karlsruhe, Germany
[4] Karlsruhe Inst Technol, D-76131 Karlsruhe, Germany
[5] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[6] NHLBI, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1083/jcb.200810060
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
How focal adhesions (FAs) convert retrograde filamentous actin (F-actin) flow into traction stress on the extracellular matrix to drive cell migration is unknown. Using combined traction force and fluorescent speckle microscopy, we observed a robust biphasic relationship between F-actin speed and traction force. F-actin speed is inversely related to traction stress near the cell edge where FAs are formed and F-actin motion is rapid. In contrast, larger FAs where the F-actin speed is low are marked by a direct relationship between F-actin speed and traction stress. We found that the biphasic switch is determined by a threshold F-actin speed of 8-10 nm/s, independent of changes in FA protein density, age, stress magnitude, assembly/disassembly status, or subcellular position induced by pleiotropic perturbations to Rho family guanosine triphosphatase signaling and myosin II activity. Thus, F-actin speed is a fundamental regulator of traction force at FAs during cell migration.
引用
收藏
页码:999 / 1005
页数:7
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