Mechanobiology of cardiomyocyte development

被引:163
作者
Jacot, Jeffrey G. [1 ,2 ]
Martin, Jody C. [3 ]
Hunt, Darlene L. [3 ]
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[2] Texas Childrens Hosp, Div Congenital Heart Surg, Houston, TX 77030 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Cardiogenesis; Rigidity; Mouse; Atomic force microscopy; Mechanotransduction; MESENCHYMAL STEM-CELLS; CYCLICAL MECHANICAL STRETCH; ATOMIC-FORCE MICROSCOPY; CARDIAC MYOCYTES; IN-VITRO; VENTRICULAR MYOCYTES; FUNCTIONAL CARDIOMYOCYTES; RAT CARDIOMYOCYTES; ISOFORM EXPRESSION; ELASTIC PROPERTIES;
D O I
10.1016/j.jbiomech.2009.09.014
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cardiac cells are under constant, self-generated mechanical stress which can affect the differentiation of stem cells into cardiac myocytes, the development of differentiated cells and the maturation of cells in neonatal mammals. In this article, the effects of direct stretch, electrically induced beating and substrate elasticity on the behavior and development of cardiomyocytes are reviewed, with particular emphasis on the effects of substrate stiffness on cardiomyocyte maturation. In order to relate these observations to in vivo mechanical conditions, we isolated the left ventricle of Black Swiss mice from embryonic day 13.5 through post-natal day 14 and measured the elastic modulus of the epicardium using atomic force microscope indentation. We found that the elastic modulus of the epicardium significantly changes at birth, from an embryonic value of 12 +/- 4 kPa to a neonatal value of 39 +/- 7 kPa. This change is in the range shown to significantly affect the development of neonatal cardiomyocytes. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:93 / 98
页数:6
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