首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Integrin-linked kinase controls vascular wall formation by negatively regulating Rho/ROCK-mediated vascular smooth muscle cell contraction.
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Integrin-linked kinase controls vascular wall formation by negatively regulating Rho/ROCK-mediated vascular smooth muscle cell contraction.

机译:整联蛋白连接的激酶通过负调节Rho / ROCK介导的血管平滑肌细胞收缩来控制血管壁形成。

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摘要

Vascular smooth muscle cells (VSMCs) form contractile layers around larger blood vessels in a process that is essential for the formation of a fully functional vasculature. Here, we show that integrin-linked kinase (ILK) is required for the formation of a unitary layer of aligned VSMCs around arterioles and the regulation of blood vessel constriction in mice. In the absence of ILK, activated Rho/ROCK signaling induces the elevated phosphorylation of myosin light chain leading to abnormally enhanced VSMC contraction in vitro and in vivo. Our findings identify ILK as a key component regulating vascular wall formation by negatively modulating VSMC contractility.
机译:血管平滑肌细胞(VSMC)在较大的血管周围形成收缩层,这是形成功能完整的脉管系统必不可少的过程。在这里,我们显示整联蛋白连接的激酶(ILK)是形成小动脉周围对齐的VSMC的统一层和调节小鼠血管收缩所必需的。在没有ILK的情况下,活化的Rho / ROCK信号传导诱导肌球蛋白轻链的磷酸化升高,从而导致体内外体内VSMC收缩异常增强。我们的发现确定ILK是通过负调节VSMC收缩力来调节血管壁形成的关键成分。

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