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显性负性c-Jun抑制血管平滑肌细胞在血小板衍生生长因子引导下的迁移。

Dominant negative c-Jun inhibits platelet-derived growth factor-directed migration by vascular smooth muscle cells.

作者信息

Ioroi Takeshi, Yamamori Motohiro, Yagi Keiko, Hirai Midori, Zhan Yumei, Kim Shokei, Iwao Hiroshi

机构信息

Department of Clinical Pharmacy, Kobe Pharmaceutical University, Kobe, Japan.

出版信息

J Pharmacol Sci. 2003 Feb;91(2):145-8. doi: 10.1254/jphs.91.145.

Abstract

The mitogen-activated protein (MAP) kinase pathways has been shown to be necessary for mitogen-stimulated proliferation, but its role in cell migration has not been fully understood. In this study, we investigated the possible contribution of signaling pathways through c-Jun in platelet-derived growth factor (PDGF)-BB directed cell migration in rat aortic vascular smooth muscle cells (VSMCs) infected with a recombinant adenovirus containing the dominant-negative c-Jun (Ad-DN-c-Jun). DN-c-Jun protein was expressed dose-dependently in VSMCs infected with Ad-DN-c-Jun. Expression of DN-c-Jun significantly inhibited VSMC migration induced by PDGF-BB. Our results provide the first evidence that signaling pathways through c-Jun participates in cell migration induced by PDGF-BB in addition to other MAP kinase pathways in VSMCs.

摘要

丝裂原活化蛋白(MAP)激酶通路已被证明是丝裂原刺激增殖所必需的,但其在细胞迁移中的作用尚未完全明确。在本研究中,我们通过感染含显性负性c-Jun(Ad-DN-c-Jun)的重组腺病毒,研究了大鼠主动脉血管平滑肌细胞(VSMC)中c-Jun信号通路在血小板衍生生长因子(PDGF)-BB介导的细胞迁移中的可能作用。DN-c-Jun蛋白在感染Ad-DN-c-Jun的VSMC中呈剂量依赖性表达。DN-c-Jun的表达显著抑制了PDGF-BB诱导的VSMC迁移。我们的结果首次证明,除了VSMC中的其他MAP激酶通路外,通过c-Jun的信号通路也参与了PDGF-BB诱导的细胞迁移。

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