Ioroi Takeshi, Yamamori Motohiro, Yagi Keiko, Hirai Midori, Zhan Yumei, Kim Shokei, Iwao Hiroshi
Department of Clinical Pharmacy, Kobe Pharmaceutical University, Kobe, Japan.
J Pharmacol Sci. 2003 Feb;91(2):145-8. doi: 10.1254/jphs.91.145.
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.
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。