Stretch-Dependent Smooth Muscle Differentiation in the Portal Vein-Role of Actin Polymerization, Calcium Signaling, and microRNAs

被引:19
|
作者
Albinsson, Sebastian [1 ]
Bhattachariya, Anirban [1 ]
Hellstrand, Per [1 ]
机构
[1] Lund Univ, Dept Expt Med Sci, S-22184 Lund, Sweden
基金
瑞典研究理事会;
关键词
vascular; smooth muscle; microRNA; actin polymerization; calcium; mechanical stretch; SUBCUTANEOUS SMALL ARTERIES; SERUM RESPONSE FACTOR; NEOINTIMAL LESION FORMATION; VASCULAR MYOGENIC RESPONSE; RESISTANCE ARTERIES; CONTRACTILE DIFFERENTIATION; ESSENTIAL-HYPERTENSION; BLOOD-PRESSURE; ORGAN-CULTURE; RAT;
D O I
10.1111/micc.12106
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mechanical forces acting on SMC in the vascular wall are known to regulate processes such as vascular remodeling and contractile differentiation. However, investigations to elucidate the underlying mechanisms of mechanotransduction in smooth muscle have been hampered by technical limitations associated with mechanical studies on pressurized small arteries, due primarily to the small amount of available tissue. The murine portal vein is a relatively large vessel showing myogenic tone that in many respects recapitulates the properties of small resistance vessels. Studies on stretched portal veins to elucidate mechanisms of mechanotransduction in the vascular wall have shown that stretch-sensitive regulation of contractile differentiation is mediated via Rho-activation and actin polymerization, while stretch-induced growth is regulated by the MAPK pathway. In this review, we have summarized findings on mechanotransduction in the portal vein with focus on stretch-induced contractile differentiation and the role of calcium, actin polymerization and miRNAs in this response.
引用
收藏
页码:230 / 238
页数:9
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