Caveolae protect endothelial cells from membrane rupture during increased cardiac output

Author:

Cheng Jade P.X.1,Mendoza-Topaz Carolina1,Howard Gillian1,Chadwick Jessica1,Shvets Elena1,Cowburn Andrew S.2,Dunmore Benjamin J.3,Crosby Alexi3,Morrell Nicholas W.3,Nichols Benjamin J.1

Affiliation:

1. Medical Research Council, Laboratory of Molecular Biology, University of Cambridge, Cambridge CB2 1TN, UK

2. Department of Physiology, University of Cambridge, Cambridge CB2 1TN, UK

3. Department of Medicine, University of Cambridge, Cambridge CB2 1TN, UK

Abstract

Caveolae are strikingly abundant in endothelial cells, yet the physiological functions of caveolae in endothelium and other tissues remain incompletely understood. Previous studies suggest a mechanoprotective role, but whether this is relevant under the mechanical forces experienced by endothelial cells in vivo is unclear. In this study we have sought to determine whether endothelial caveolae disassemble under increased hemodynamic forces, and whether caveolae help prevent acute rupture of the plasma membrane under these conditions. Experiments in cultured cells established biochemical assays for disassembly of caveolar protein complexes, and assays for acute loss of plasma membrane integrity. In vivo, we demonstrate that caveolae in endothelial cells of the lung and cardiac muscle disassemble in response to acute increases in cardiac output. Electron microscopy and two-photon imaging reveal that the plasma membrane of microvascular endothelial cells in caveolin 1−/− mice is much more susceptible to acute rupture when cardiac output is increased. These data imply that mechanoprotection through disassembly of caveolae is important for endothelial function in vivo.

Publisher

Rockefeller University Press

Subject

Cell Biology

Reference47 articles.

1. Differential dependence of stretch and shear stress signaling on caveolin-1 in the vascular wall;Albinsson;Am. J. Physiol. Cell Physiol.,2008

2. Damage control: cellular mechanisms of plasma membrane repair;Andrews;Trends Cell Biol.,2014

3. Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy;Ardissone;BMC Med. Genet.,2013

4. Whole exome sequencing to identify a novel gene (caveolin-1) associated with human pulmonary arterial hypertension;Austin;Circ Cardiovasc Genet.,2012

5. Clathrin-independent pathways do not contribute significantly to endocytic flux;Bitsikas;eLife.,2014

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