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首页> 外文期刊>FEBS Open Bio >Activation of Notch3 promotes pulmonary arterial smooth muscle cells proliferation via Hes1/p27Kip1 signaling pathway
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Activation of Notch3 promotes pulmonary arterial smooth muscle cells proliferation via Hes1/p27Kip1 signaling pathway

机译:Notch3的激活通过Hes1 / p27Kip1信号通路促进肺动脉平滑肌细胞增殖

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Activation of the Notch3 cascade is involved in the development of pulmonary arterial hypertension by stimulating the proliferation of vascular smooth muscle cells. However, the detailed molecular mechanisms underlying this effect are still unclear. The present study aims to address this issue. We demonstrated that over-expression of intracellular domain of the Notch3 receptor (NICD3) by adenovirus transfection dramatically induced proliferation of primary cultured pulmonary artery smooth muscle cells. This was accompanied with up-regulation of Hes1 protein and down-regulation of p27Kip1 protein. More importantly, we observed that prior silencing of Hes1 with siRNA blocked NICD3 over-expression-induced p27Kip1 reduction and cell proliferation. The present study suggests that Hes1 lies downstream of NICD3 and particularly mediates Notch3 signaling-induced proliferation of pulmonary arterial smooth muscle cells by down-regulation of p27Kip1 expression.
机译:Notch3级联的激活通过刺激血管平滑肌细胞的增殖而参与肺动脉高压的发展。但是,尚不清楚这种作用的详细分子机制。本研究旨在解决这个问题。我们证明了腺病毒转染Notch3受体(NICD3)的胞内域的过表达极大地诱导了原代培养的肺动脉平滑肌细胞的增殖。这伴随着Hes1蛋白的上调和p27Kip1蛋白的下调。更重要的是,我们观察到用siRNA沉默Hes1可以阻止NICD3过表达诱导的p27Kip1减少和细胞增殖。本研究表明,Hes1位于NICD3的下游,并通过下调p27Kip1表达来介导Notch3信号诱导的肺动脉平滑肌细胞增殖。

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