Cell-Matrix Interactions in the Pathobiology of Calcific Aortic Valve Disease Critical Roles for Matricellular, Matricrine, and Matrix Mechanics Cues

被引:230
作者
Chen, Jan-Hung [1 ,2 ]
Simmons, Craig A. [1 ,2 ,3 ]
机构
[1] Univ Toronto, Dept Mech & Ind Engn, Toronto, ON M5S 3G8, Canada
[2] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON M5S 3G8, Canada
[3] Univ Toronto, Fac Dent, Toronto, ON M5S 3G8, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
biomechanics; calcific aortic valve disease; extracellular matrix; matricellular signaling; matricrine signaling; VALVULAR INTERSTITIAL CELL; GROWTH-FACTOR-BETA; ELASTOLYTIC CATHEPSIN-S; EXTRACELLULAR-MATRIX; HEART-VALVE; TENASCIN-C; TRANSFORMING GROWTH-FACTOR-BETA-1; ENDOTHELIAL-CELLS; CHONDROMODULIN-I; METALLOPROTEINASE EXPRESSION;
D O I
10.1161/CIRCRESAHA.110.234237
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The hallmarks of calcific aortic valve disease (CAVD) are the significant changes that occur in the organization, composition, and mechanical properties of the extracellular matrix (ECM), ultimately resulting in stiffened stenotic leaflets that obstruct flow and compromise cardiac function. Increasing evidence suggests that ECM maladaptations are not simply a result of valve cell dysfunction; they also contribute to CAVD progression by altering cellular and molecular signaling. In this review, we summarize the ECM changes that occur in CAVD. We also discuss examples of how the ECM influences cellular processes by signaling through adhesion receptors (matricellular signaling), by regulating the presentation and availability of growth factors and cytokines to cells (matricrine signaling), and by transducing externally applied forces and resisting cell-generated tractional forces (mechanical signaling) to regulate a wide range of pathological processes, including differentiation, fibrosis, calcification, and angiogenesis. Finally, we suggest areas for future research that should lead to new insights into bidirectional cell-ECM interactions in the aortic valve, their contributions to homeostasis and pathobiology, and possible targets to slow or prevent the progression of CAVD. (Circ Res. 2011;108:1510-1524.)
引用
收藏
页码:1510 / 1524
页数:15
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