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首页> 外文期刊>Marine Drugs >Dihydroaustrasulfone Alcohol Inhibits PDGF-Induced Proliferation and Migration of Human Aortic Smooth Muscle Cells through Inhibition of the Cell Cycle
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Dihydroaustrasulfone Alcohol Inhibits PDGF-Induced Proliferation and Migration of Human Aortic Smooth Muscle Cells through Inhibition of the Cell Cycle

机译:二氢autrasulfone酒精通过抑制细胞周期抑制PDGF诱导的人主动脉平滑肌细胞的增殖和迁移。

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Dihydroaustrasulfone alcohol is the synthetic precursor of austrasulfone, which is a marine natural product, isolated from the Taiwanese soft coral Cladiella australis. Dihydroaustrasulfone alcohol has anti-inflammatory, neuroprotective, antitumor and anti-atherogenic properties. Although dihydroaustrasulfone alcohol has been shown to inhibit neointima formation, its effect on human vascular smooth muscle cells (VSMCs) has not been elucidated. We examined the effects and the mechanisms of action of dihydroaustrasulfone alcohol on proliferation, migration and phenotypic modulation of human aortic smooth muscle cells (HASMCs). Dihydroaustrasulfone alcohol significantly inhibited proliferation, DNA synthesis and migration of HASMCs, without inducing cell death. Dihydroaustrasulfone alcohol also inhibited platelet-derived growth factor (PDGF)-induced expression of cyclin-dependent kinases (CDK) 2, CDK4, cyclin D1 and cyclin E. In addition, dihydroaustrasulfone alcohol inhibited PDGF-induced phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2), whereas it had no effect on the phosphorylation of phosphatidylinositol 3-kinase (PI3K)/(Akt). Moreover, treatment with PD98059, a highly selective ERK inhibitor, blocked PDGF-induced upregulation of cyclin D1 and cyclin E and downregulation of p27kip1. Furthermore, dihydroaustrasulfone alcohol also inhibits VSMC synthetic phenotype formation induced by PDGF. For in vivo studies, dihydroaustrasulfone alcohol decreased smooth muscle cell proliferation in a rat model of restenosis induced by balloon injury. Immunohistochemical staining showed that dihydroaustrasulfone alcohol noticeably decreased the expression of proliferating cell nuclear antigen (PCNA) and altered VSMC phenotype from a synthetic to contractile state. Our findings provide important insights into the mechanisms underlying the vasoprotective actions of dihydroaustrasulfone alcohol and suggest that it may be a useful therapeutic agent for the treatment of vascular occlusive disease.
机译:二氢金砜砜醇是从台湾软珊瑚澳大藻克拉迪藻中分离出来的一种海洋天然产物,奥氏砜的合成前体。二氢金砜砜醇具有抗炎,神经保护,抗肿瘤和抗动脉粥样硬化特性。尽管已证明二氢金磺砜醇抑制新内膜形成,但尚未阐明其对人血管平滑肌细胞(VSMC)的作用。我们检查了对人类主动脉平滑肌细胞(HASMCs)增殖,迁移和表型调节的二氢金刚烷醇的作用及其作用机理。二氢金砜砜醇显着抑制HASMC的增殖,DNA合成和迁移,而不会引起细胞死亡。二氢金刚烷醇还抑制血小板衍生的生长因子(PDGF)诱导的细胞周期蛋白依赖性激酶(CDK)2,CDK4,cyclin D1和cyclin E的表达。此外,二氢金刚烷醇抑制PDGF诱导的细胞外信号调节激酶1的磷酸化。 / 2(ERK1 / 2),而对磷脂酰肌醇3-激酶(PI3K)/(Akt)的磷酸化没有影响。此外,高选择性ERK抑制剂PD98059的治疗可阻止PDGF诱导的细胞周期蛋白D1和细胞周期蛋白E的上调以及p27 kip1 的下调。此外,二氢金砜砜醇也抑制由PDGF诱导的VSMC合成表型的形成。为了进行体内研究,在由球囊损伤引起的再狭窄的大鼠模型中,二氢金刚烷醇降低了平滑肌细胞的增殖。免疫组织化学染色显示,二氢金砜砜醇明显降低了增殖细胞核抗原(PCNA)的表达,并将VSMC表型从合成状态转变为收缩状态。我们的研究结果提供了重要的见解,对二氢金磺砜醇的血管保护作用的潜在机制,并表明它可能是治疗血管闭塞性疾病的有用治疗剂。

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