| Literature DB >> 11271503 |
J Yin1, C McLachlan, X Chaufour, M A McGuire, G White, V Turner, N J King, B D Hambly.
Abstract
Proliferation and migration of vascular smooth muscle cells (VSMCs) are involved in the processes of atherosclerosis and restenosis. The protein product of the growth arrest-specific gene 6 (Gas-6) has recently been identified as a ligand for the Axl/Rse/Mer tyrosine kinase receptor family, which may be involved in proliferation and migration of VSMCs. Here we show that Gas-6 gene expression is increased in proliferating VSMCs in tissue culture (2.5-fold increase by Northern blot) and following neointimal proliferation in a rabbit balloon-injury model (3-fold increase by Western blot). Neither platelet-derived growth factor (PDGF) nor thrombin stimulate the expression of Gas-6 in cultured VSMCs despite the ability of the PDGF, but not thrombin, to stimulate proliferation in growth-arrested cells. These data suggest a role for the Gas-6 regulatory system in VSMC proliferation, which may be a target for therapeutic interventions in the atherosclerotic process and restenosis after angioplasty.Entities:
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Year: 2000 PMID: 11271503 DOI: 10.1002/1522-2683(200011)21:17<3851::AID-ELPS3851>3.0.CO;2-Q
Source DB: PubMed Journal: Electrophoresis ISSN: 0173-0835 Impact factor: 3.535