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

Author:

Oakes Patrick W.111,Beckham Yvonne11,Stricker Jonathan111,Gardel Margaret L.111

Affiliation:

1. Institute for Biophysical Dynamics, Department of Physics, and The James Franck Institute, University of Chicago, Chicago, IL 60637

Abstract

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 α-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.

Publisher

Rockefeller University Press

Subject

Cell Biology

Reference50 articles.

1. Phosphorylation of platelet myosin increases actin-activated myosin ATPase activity;Adelstein;Nature.,1975

2. Formation of actin stress fibers and focal adhesions enhanced by Rho-kinase;Amano;Science.,1997

3. Transient frictional slip between integrin and the ECM in focal adhesions under myosin II tension;Aratyn-Schaus;Curr. Biol.,2010

4. Preparation of complaint matrices for quantifying cellular contraction;Aratyn-Schaus;J. Vis. Exp.,2010

5. Dynamic and structural signatures of lamellar actomyosin force generation;Aratyn-Schaus;Mol. Biol. Cell.,2011

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3