Stimulation of vascular smooth muscle cell migration by macrophage migration inhibitory factor

被引:21
|
作者
Schrans-Stassen, BHGJ
Lue, H
Sonnemans, DGP
Bernhagen, J
Post, MJ
机构
[1] Maastricht Univ, Dept Physiol, NL-6200 MD Maastricht, Netherlands
[2] Interuniv Cardiol Inst Netherlands, Cardiovasc Res Inst Maastricht, Dept Mol & Expt Cardiol, NL-6200 MD Maastricht, Netherlands
[3] Univ Hosp RWTH Aachen, Inst Biochem, Div Biochem & Mol Cell Biol, Aachen, Germany
关键词
D O I
10.1089/ars.2005.7.1211
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
Macrophage migration inhibitory factor (MIF) is a well known proinflammatory factor that influences the migration and proliferation of various cell types, predominantly monocytes and macrophages. Recent evidence suggests an important role for MIF in the progression of atherosclerosis and restenosis. For this reason, we studied the effect of MIF on platelet-derived growth factor-BB (PDGF-BB)-induced migration and PDGF receptor protein expression in vascular smooth muscle cells (VSMCs). Furthermore, the possibility of MIF influencing the migration of VSMCs was investigated. Our results show that short-term incubation of MIF is able to enhance PDGF-BB-induced migration. Long-term incubation decreases PDGF-BB-induced migration, but preserves a short-term stimulatory effect. These effects are not regulated at the level of PDGF receptor protein expression. MIF also acts as a chemoattractant for VSMCs, with a maximum response at 15 ng/ml. In contrast, the proliferation of VSMCs was unaffected by MIF. We conclude that MIF has a biphasic effect on VSMC migration. It remains unclear whether this effect is direct or involves the secretion of unidentified promigratory factors. Exogenous MIF does not stimulate VSMC proliferation; however, a role for MIF in proliferation cannot be fully ruled out. In view of the known key contributions of macrophage-derived MIF and VSMCs, the observed effects may well play a role in the progression of atherosclerosis and restenosis.
引用
收藏
页码:1211 / 1216
页数:6
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