The role of extracellular matrix stiffness in regulating cytoskeletal remodeling via vinculin in synthetic smooth muscle cells

被引:18
|
作者
Shen, Kai [1 ]
Kenche, Harshavardhan [1 ]
Zhao, Hua [2 ]
Li, Jinping [3 ]
Stone, Jasimine [1 ]
机构
[1] Savannah State Univ, Dept Chem & Forens Sci, Savannah, GA 31404 USA
[2] Univ Northern Colorado, Dept Chem & Biochem, Greeley, CO 80639 USA
[3] Mercer Univ, Dept Biomed Sci, Sch Med, Savannah, GA 31404 USA
基金
美国国家卫生研究院;
关键词
Extracellular matrix; Stiffness; Synthetic vascular smooth muscle cells; Vinculin; AORTIC STIFFNESS; PROTEIN; EXPRESSION; ACTIN; HYPERTENSION; DISPARITIES; MIGRATION; MOTILITY; GROWTH; DIFFER;
D O I
10.1016/j.bbrc.2018.11.142
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vinculin is a key player in sensing and responding to external mechanical cues such as extracellular matrix stiffness. Increased matrix stiffness is often associated with certain pathological conditions including hypertension induced cellular cytoskeleton changes in vascular smooth muscle (VSM) cells. However, little is known on how stiffness affects cytoskeletal remodeling via vinculin in VSM cells. Thus, we utilized matrices with elastic moduli that simulate vascular stiffness in different stages of hypertension to investigate how matrix stiffness regulates cell cytoskeleton via vinculin in synthetic VSM cells. Through selecting a suitable reference gene, we found that an increase in physiologically relevant extracellular matrix stiffness (2-50 kPa) downregulates vinculin gene expression but upregulates vinculin protein expression. This discrepancy, which was not observed previously for non-muscle cells, suggests that the vinculin-mediated mecahnotransduction mechanism in synthetic VSM cells may be more complex than those proposed for non-muscle cells. Also adding to previous findings, we found that VSM cell growth may be impeded by substrates that are either too soft or too rigid. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:302 / 307
页数:6
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