Angiotensin II-induced smooth muscle cell migration is mediated by LDL receptor-related protein 1 via regulation of matrix metalloproteinase 2 expression

被引：14

作者：

Jung, Hae Ok ^{[1
]}

Uhm, Jae Sun ^{[1
]}

Seo, Suk Min ^{[1
]}

Kim, Jee Hee ^{[1
]}

Youn, Ho-Joong ^{[1
]}

Baek, Sang Hong ^{[1
]}

Chung, Wook Sung ^{[1
]}

Seung, Ki Bae ^{[1
]}

机构：

[1] Catholic Univ Korea, Ctr Cardiovasc, Seoul St Marys Hosp, Coll Med, Seoul 137701, South Korea

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 2010年 / 402卷 / 04期

关键词：

Smooth muscle cells; Migration; LRP1; Angiotensin II; Matrix metalloproteinase 2; UROKINASE RECEPTOR; ALPHA(2)-MACROGLOBULIN RECEPTOR; PLASMINOGEN-ACTIVATOR; VASCULAR WALL; INVASION; ATHEROSCLEROSIS; CARCINOMA; COMPLEX;

D O I：

10.1016/j.bbrc.2010.10.019

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：

Anglotensin II (Ang II) one of the main vasoactive hormones of the renin-angiotensin system contributes to the development and progression of atherosclerosis by inducing vascular smooth muscle cells (VSMCs) migration Although previous studies have shown that Ang II upregulates low density lipoprotein receptor-related protein 1 (LRP1) expression in VSMCs and increases VSMCs migration the role of LRP1 in Ang II-induced VSMCs migration remains unclear Here we reveal a novel mechanism by which LRP1 induces the expression of matrix metalloproteinase 2 (MMP2) and thereby promotes the migration of rat aortic SMCs (RAoSMCs) Knockdown of LRP1 expression greatly decreased RAoSMCs migration which was rescued by forced expression of a functional LRP1 minireceptor suggesting that LRP1 is a key regulator of Ang II-induced RAoSMCs migration Inhibition of ligand binding to LRP1 by the specific antagonist receptor-associated protein (RAP) also led to reduced RAoSMCs migration Because MMPs play critical roles in RAoSMCs migration we examined the expression of several MMPs and found that the expression of functional MMP2 was selectively increased by Ang II treatment and decreased in LRP1-knockdown RAoSMCs More interestingly reduced MMP2 expression in LRP1-knockdown cells was completely rescued by exogenous expression of mLRP4 suggesting that MMP2 is a downstream regulator of LRP1 in Ang II-induced RAoSMCs migration Together our data strongly suggest that LRP1 promotes the migration of RAoSMCs by regulating the expression and function of MMP2 (C) 2010 Elsevier Inc All rights reserved

引用

页码：577 / 582

页数：6

共 26 条

[21] Reactive Oxygen Species Inhibit Adhesion of Mesenchymal Stem Cells Implanted into Ischemic Myocardium via Interference of Focal Adhesion Complex [J].