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人类三泽蛋白-1通过丝裂原活化蛋白激酶信号通路控制平滑肌细胞的增殖和趋化性。

Human tribbles-1 controls proliferation and chemotaxis of smooth muscle cells via MAPK signaling pathways.

作者信息

Sung Hye Youn, Guan Hongtao, Czibula Agnes, King Andrea R, Eder Katalin, Heath Emily, Suvarna S Kim, Dower Steven K, Wilson Anthony G, Francis Sheila E, Crossman David C, Kiss-Toth Endre

机构信息

Cardiovascular Research Unit, University of Sheffield, Sheffield S10 2TN, United Kingdom.

Section of Infection, Inflammation and Immunity, University of Sheffield, Sheffield S10 2TN, United Kingdom.

出版信息

J Biol Chem. 2007 Jun 22;282(25):18379-18387. doi: 10.1074/jbc.M610792200. Epub 2007 Apr 23.

Abstract

Migration and proliferation of smooth muscle cells are key to a number of physiological and pathological processes, including wound healing and the narrowing of the vessel wall. Previous work has shown links between inflammatory stimuli and vascular smooth muscle cell proliferation and migration through mitogen-activated protein kinase (MAPK) activation, although the molecular mechanisms of this process are poorly understood. Here we report that tribbles-1, a recently described modulator of MAPK activation, controls vascular smooth muscle cell proliferation and chemotaxis via the Jun kinase pathway. Our findings demonstrate that this regulation takes place via direct interactions between tribbles-1 and MKK4/SEK1, a Jun activator kinase. The activity of this kinase is dependent on tribbles-1 levels, whereas the activation and the expression of MKK4/SEK1 are not. In addition, tribbles-1 expression is elevated in human atherosclerotic arteries when compared with non-atherosclerotic controls, suggesting that this protein may play a role in disease in vivo. In summary, the data presented here suggest an important regulatory role for trb-1 in vascular smooth muscle cell biology.

摘要

平滑肌细胞的迁移和增殖是许多生理和病理过程的关键,包括伤口愈合和血管壁狭窄。先前的研究表明,炎症刺激与血管平滑肌细胞增殖和迁移之间存在联系,这一过程通过丝裂原活化蛋白激酶(MAPK)激活介导,尽管该过程的分子机制尚不清楚。在此,我们报告tribbles-1(一种最近描述的MAPK激活调节剂)通过Jun激酶途径控制血管平滑肌细胞增殖和趋化性。我们的研究结果表明,这种调节是通过tribbles-1与MKK4/SEK1(一种Jun激活激酶)之间的直接相互作用实现的。该激酶的活性依赖于tribbles-1水平,而MKK4/SEK1的激活和表达则不受其影响。此外,与非动脉粥样硬化对照相比,人动脉粥样硬化动脉中tribbles-1表达升高,这表明该蛋白可能在体内疾病中发挥作用。总之,本文提供的数据表明trb-1在血管平滑肌细胞生物学中具有重要的调节作用。

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