Abstract

Connective tissue growth factor (CTGF) is abundantly expressed in the vascular smooth muscle cells (VSMC) of atherosclerotic lesions but not in normal vessels. CTGF is able to promote VSMC proliferation and migration and influences the composition of extracellular matrix. The mechanisms for controlling these events remain unclear. We studied the effects of CTGF on matrix metalloproteinases (MMPs) by introducing a CTGF over-expression construct into VSMC. We found that the over-expression of CTGF significantly increased the activity of MMP-2 in VSMC conditioned medium. MMP-2 activity was similarly increased by exogenous CTGF treatment, and this effect could be blocked by an anti-CTGF antibody. We also showed that the increased MMP-2 activity was due to an increase in MMP-2 mRNA levels in VSMC. We further studied the mechanisms involved in the regulation of MMP-2 mRNA levels and found that the AP-2 transcription factor is responsible for most of the CTGF-induced MMP-2 transcription. Because MMP-2 is an important factor directly involved in controlling cell movement and the turnover of extracellular matrix, our study may provide a mechanism for CTGF-promoted VSMC migration.

Highlights

  • We have found that Connective tissue growth factor (CTGF) increases the activity of matrix metalloproteinases (MMPs)-2 in vascular smooth muscle cells (VSMC) conditioned medium, and this increase is the result of rising level of MMP-2 mRNA

  • Because MMP-2 is intimately involved in promoting VSMC migration during neointima formation, our results suggest that CTGF-promoted VSMC migration is mediated by MMP-2

  • MMP-2 Expression Is Increased in CTGF Over-expression VSMC—To study the functions of CTGF, we stably transfected a CTGF over-expression construct into VSMC

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Summary

Introduction

In studying occlusive vascular disease, much attention has been focused on increased MMP-2 expression and its ability to promote VSMC migration to the intima from the original media after either inflammatory or mechanical injury to the vascular wall (6, 7). MMP-2 expression in VSMC is up-regulated by vascular injury and low blood flow conditions but is down-regulated by cellular differentiation and high blood flow (11). The mechanism for this regulation, is unclear. Recent advances have shown that CTGF is involved in diverse autocrine or paracrine actions in many cell types such as vascular endothelial cells, epithelial cells, neuronal cells, VSMC, and cells of supportive skeletal tissues (see review in Ref. 13). Because MMP-2 is intimately involved in promoting VSMC migration during neointima formation, our results suggest that CTGF-promoted VSMC migration is mediated by MMP-2

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