On Valve Interstitial Cell Signaling: The Link Between Multiscale Mechanics and Mechanobiology

被引:8
|
作者
Howsmon, Daniel P. [1 ,2 ]
Sacks, Michael S. [1 ,2 ]
机构
[1] Univ Texas Austin, James T Willerson Ctr Cardiovasc Modeling & Simul, Oden Inst Computat Engn & Sci, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
关键词
Valve interstitial cell; Mechanobiology; Cell signaling; Systems biology; AORTIC-VALVE; MYOFIBROBLAST DIFFERENTIATION; SYSTEMS BIOLOGY; ACTIVATION; PHENOTYPE; STIFFNESS; CALCIFICATION; GROWTH; YAP; FIBROBLASTS;
D O I
10.1007/s13239-020-00509-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Heart valves function in one of the most mechanically demanding environments in the body to ensure unidirectional blood flow. The resident valve interstitial cells respond to this mechanical environment and maintain the structure and integrity of the heart valve tissues to preserve homeostasis. While the mechanics of organ-tissue-cell heart valve function has progressed, the intracellular signaling network downstream of mechanical stimuli has not been fully elucidated. This has hindered efforts to both understand heart valve mechanobiology and rationally identify drug targets for treating valve disease. In the present work, we review the current literature on VIC mechanobiology and then propose mechanistic mathematical modeling of the mechanically-stimulated VIC signaling response to comprehend the coupling between VIC mechanobiology and valve mechanics.
引用
收藏
页码:15 / 27
页数:13
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