Yin J, McLachlan C, Chaufour X, McGuire M A, White G, Turner V, King N J, Hambly B D
Department of Pathology, University of Sydney, Australia.
Electrophoresis. 2000 Nov;21(17):3851-6. doi: 10.1002/1522-2683(200011)21:17<3851::AID-ELPS3851>3.0.CO;2-Q.
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.
血管平滑肌细胞(VSMC)的增殖和迁移参与动脉粥样硬化和再狭窄的过程。生长停滞特异性基因6(Gas-6)的蛋白质产物最近被确定为Axl/Rse/Mer酪氨酸激酶受体家族的配体,这可能参与VSMC的增殖和迁移。在这里,我们表明,在组织培养中增殖的VSMC中,Gas-6基因表达增加(Northern印迹法显示增加2.5倍),在兔球囊损伤模型中内膜增生后也增加(Western印迹法显示增加3倍)。尽管血小板衍生生长因子(PDGF)能够刺激生长停滞细胞的增殖,但血小板衍生生长因子和凝血酶均不能刺激培养的VSMC中Gas-6的表达。这些数据表明Gas-6调节系统在VSMC增殖中起作用,这可能是动脉粥样硬化过程和血管成形术后再狭窄治疗干预的靶点。