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Tissue inhibitor of metalloproteinases-4 suppresses vascular smooth muscle cell migration and induces cell apoptosis

机译:金属蛋白酶4的组织抑制剂抑制血管平滑肌细胞迁移并诱导细胞凋亡

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摘要

In a previous study, we have demonstrated that overexpression of the tissue inhibitors of metalloproteinases-4 (TIMP-4) can inhibit the neointima, formation in the rat carotid model. To define the functions of tissue inhibitor of metalloproteinases-4 (TIMP-4) in SMCs, we transduced human TIMP-4 cDNA into rat aortic SMCs by using adenoviral vector. Overexpression of TIMP-4 blocked the conversion of pro-MMP-2 to the active form and inhibited basic fibroblast growth factor-induced migration by 56.7% (p<0.01). Overexpression of TIMP-4 markedly increased apoptotic cell death without changing their proliferation. Importantly, overexpression of human TIMP-4 in the wall of balloon-injured rat carotid artery also increased SMC apoptosis. The percentages of TUNEL-positive cells of total cells increased significantly in AdTIMP-4 infected group compared with AdGFP infected group. These findings demonstrate that TIMP-4 can inhibit SMCs migration and induce apoptosis in vitro and in vivo, which may generate new targets for prevention and treatment of vascular diseases. (C) 2004 Elsevier Inc. All rights reserved.
机译:在以前的研究中,我们已经证明金属蛋白酶4(TIMP-4)的组织抑制剂的过表达可以抑制大鼠颈动脉模型中新内膜的形成。为了定义金属蛋白酶-4(TIMP-4)在SMC中的组织功能,我们使用腺病毒载体将人TIMP-4 cDNA转导到大鼠主动脉SMC中。 TIMP-4的过表达阻止pro-MMP-2转化为活性形式,并抑制碱性成纤维细胞生长因子诱导的迁移56.7%(p <0.01)。 TIMP-4的过表达显着增加了凋亡细胞的死亡而没有改变它们的增殖。重要的是,人TIMP-4在球囊损伤的大鼠颈动脉壁中的过表达也增加了SMC的细胞凋亡。与AdGFP感染组相比,AdTIMP-4感染组总细胞中TUNEL阳性细胞的百分比显着增加。这些发现表明TIMP-4可以抑制SMCs迁移并在体内和体外诱导细胞凋亡,这可能产生预防和治疗血管疾病的新靶标。 (C)2004 Elsevier Inc.保留所有权利。

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