Tension is required but not sufficient for focal adhesion maturation without a stress fiber template

被引:241
作者
Oakes, Patrick W. [1 ,2 ,3 ]
Beckham, Yvonne [1 ,3 ]
Stricker, Jonathan [1 ,2 ,3 ]
Gardel, Margaret L. [1 ,2 ,3 ]
机构
[1] Univ Chicago, Inst Biophys Dynam, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Phys, Chicago, IL 60637 USA
[3] Univ Chicago, James Franck Inst, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
ACTIN-FILAMENTS; ALPHA-ACTININ; DYNAMICS; PAXILLIN; GROWTH; FORCE; PHOSPHORYLATION; INTEGRIN; MATRIX; ORGANIZATION;
D O I
10.1083/jcb.201107042
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Focal adhesion composition and size are modulated in a myosin II-dependent maturation process that controls adhesion, migration, and matrix remodeling. As myosin II activity drives stress fiber assembly and enhanced tension at adhesions simultaneously, the extent to which adhesion maturation is driven by tension or altered actin architecture is unknown. We show that perturbations to formin and alpha-actinin 1 activity selectively inhibited stress fiber assembly at adhesions but retained a contractile lamella that generated large tension on adhesions. Despite relatively unperturbed adhesion dynamics and force transmission, impaired stress fiber assembly impeded focal adhesion compositional maturation and fibronectin remodeling. Finally, we show that compositional maturation of focal adhesions could occur even when myosin II-dependent cellular tension was reduced by 80%. We propose that stress fiber assembly at the adhesion site serves as a structural template that facilitates adhesion maturation over a wide range of tensions. This work identifies the essential role of lamellar actin architecture in adhesion maturation.
引用
收藏
页码:363 / 374
页数:12
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