The mechanobiology of mitral valve function, degeneration, and repair

被引:25
作者
Richards, Jennifer M. [1 ]
Farrar, Emily J. [1 ]
Kornreich, Bruce G. [2 ]
Moise, N. Sydney [2 ]
Butcher, Jonathan T. [1 ]
机构
[1] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[2] Cornell Univ, Coll Vet Med, Dept Clin Sci, Cardiol Sect, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
Strain; Stress; Myxomatous; Biomechanics; Myofibroblast; VALVULAR INTERSTITIAL-CELLS; TO-EDGE REPAIR; MECHANICAL-PROPERTIES; ANTERIOR LEAFLET; HEART-FAILURE; IN-VIVO; DISEASE; COLLAGEN; STRAIN; SIZE;
D O I
10.1016/j.jvc.2012.01.002
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
In degenerative valve disease, the highly organized mitral valve leaflet matrix stratification is progressively destroyed and replaced with proteoglycan rich, mechanically inadequate tissue. This is driven by the actions of originally quiescent valve interstitial cells that become active contractile and migratory myofibroblasts. White treatment for myxomatous mitral valve disease in humans ranges from repair to total replacement, therapies in dogs focus on treating the consequences of the resulting mitral regurgitation. The fundamental gap in our understanding is how the resident valve cells respond to altered mechanical signals to drive tissue remodeling. Despite the pathological similarities and high clinical occurrence, surprisingly little mechanistic insight has been gleaned from the dog. This review presents what is known about mitral valve mechanobiology from clinical, in vivo, and in vitro data. There are a number of experimental strategies already available to pursue this significant opportunity, but success requires the collaboration between veterinary clinicians, scientists, and engineers. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 58
页数:12
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