Model of cellular mechanotransduction via actin stress fibers

被引:0
作者
Cecile L. M. Gouget
Yongyun Hwang
Abdul I. Barakat
机构
[1] Ecole Polytechnique,Hydrodynamics Laboratory (LadHyX), Department of Mechanics
[2] CNRS UMR7646,Department of Aeronautics, Faculty of Engineering
[3] Imperial College,undefined
来源
Biomechanics and Modeling in Mechanobiology | 2016年 / 15卷
关键词
Mechanotransduction; Stress fibers; Cytoskeleton ; Endothelial cells; Mechanical model; Force transmission;
D O I
暂无
中图分类号
学科分类号
摘要
Mechanical stresses due to blood flow regulate vascular endothelial cell structure and function and play a key role in arterial physiology and pathology. In particular, the development of atherosclerosis has been shown to correlate with regions of disturbed blood flow where endothelial cells are round and have a randomly organized cytoskeleton. Thus, deciphering the relation between the mechanical environment, cell structure, and cell function is a key step toward understanding the early development of atherosclerosis. Recent experiments have demonstrated very rapid (∼\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\sim $$\end{document}100 ms) and long-distance (∼\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\sim $$\end{document}10 μ\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\upmu $$\end{document}m) cellular mechanotransduction in which prestressed actin stress fibers play a critical role. Here, we develop a model of mechanical signal transmission within a cell by describing strains in a network of prestressed viscoelastic stress fibers following the application of a force to the cell surface. We find force transmission dynamics that are consistent with experimental results. We also show that the extent of stress fiber alignment and the direction of the applied force relative to this alignment are key determinants of the efficiency of mechanical signal transmission. These results are consistent with the link observed experimentally between cytoskeletal organization, mechanical stress, and cellular responsiveness to stress. Based on these results, we suggest that mechanical strain of actin stress fibers under force constitutes a key link in the mechanotransduction chain.
引用
收藏
页码:331 / 344
页数:13
相关论文
共 255 条
[1]  
Ashkin A(1990)Force generation of organelle transport measured in vivo by an infrared laser trap Nature 348 346-348
[2]  
Schütze K(2006)Secrets of the code: Do vascular endothelial cells use ion channels to decipher complex flow signals? Biomaterials 27 671-678
[3]  
Dziedzic J(2006)Isostaticity and controlled force transmission in the cytoskeleton: a model awaiting experimental evidence Biophys J 91 1970-1983
[4]  
Euteneuer U(1969)Arterial wall shear and distribution of early atheroma in man Nature 223 1159-1161
[5]  
Schliwa M(2007)Role of endothelial shear stress in the natural history of coronary atherosclerosis and vascular remodeling J Am Coll Cardiol 49 2379-2393
[6]  
Barakat AI(2007)Mechanotransduction and endothelial cell homeostasis: the wisdom of the cell Am J Physiol Heart Circ Physiol 292 H1209-H1224
[7]  
Lieu DK(1997)Extracellular matrix rigidity causes strengthening of integrin-cytoskeleton linkages Cell 88 39-48
[8]  
Gojova A(2009)Mechanosensing in actin stress fibers revealed by a close correlation between force and protein localization J Cell Sci 122 1665-1679
[9]  
Blumenfeld R(1992)Human endothelial cells express integrin receptors on the luminal aspect of their membrane Blood 80 437-446
[10]  
Caro C(2006)Dynamic regulation of ERK2 nuclear translocation and mobility in living cells J Cell Sci 119 4952-4963