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跨膜4超家族成员5(TM4SF5)通过胞质p27Kip1表达和RhoA活性加速G1/S期进程。

TM4SF5 accelerates G1/S phase progression via cytosolic p27Kip1 expression and RhoA activity.

作者信息

Kim Hyeonjung, Kang Minkyung, Lee Sin-Ae, Kwak Tae Kyoung, Jung Oisun, Lee Hyo Jeong, Kim Sung-Hoon, Lee Jung Weon

机构信息

Department of Tumor Biology, Cancer Research Institute, Cell Dynamics Research Center, College of Medicine, Seoul National University, Seoul 151-742, Republic of Korea.

出版信息

Biochim Biophys Acta. 2010 Aug;1803(8):975-82. doi: 10.1016/j.bbamcr.2010.04.001. Epub 2010 Apr 22.

Abstract

Transmembrane 4 L six family member 5 (TM4SF5) causes epithelial-mesenchymal transition (EMT) for aberrant cell proliferation. However, the effects of TM4SF5 expression on cell cycle are unknown so far. In this study, using hepatocytes that either ectopically or endogenously express TM4SF5 and human hepatocarcinoma tissues, the role of TM4SF5 in G1/S phase progression was examined. We found that TM4SF5 expression accelerated G1/S phase progression with facilitated cyclin D1 and E expression and Rb phosphorylation. Furthermore, TM4SF5 enhanced trafficking of CDK4 and cyclin D1 into the nucleus and induced complex formation between them. However, TM4SF5-facilitated G1/S phase progression was blocked by silencing of p27Kip1 using siRNA or by infection of active RhoA. Pharmacological inhibition of ROCK accelerated the G1/S phase progression of control TM4SF5-unexpressing cells. Altogether, these observations suggest that TM4SF5 accelerates G1/S phase progression with facilitated CDK4/cyclin D1 entry into the nucleus, which might be supported by TM4SF5-mediated actin reorganization through cytosolic p27Kip1 expression and Rho GTPase activity.

摘要

跨膜4 L六家族成员5(TM4SF5)通过上皮-间质转化(EMT)导致异常细胞增殖。然而,目前TM4SF5表达对细胞周期的影响尚不清楚。在本研究中,利用异位或内源性表达TM4SF5的肝细胞以及人肝癌组织,研究了TM4SF5在G1/S期进程中的作用。我们发现,TM4SF5的表达通过促进细胞周期蛋白D1和E的表达以及Rb磷酸化,加速了G1/S期进程。此外,TM4SF5增强了CDK4和细胞周期蛋白D1向细胞核的转运,并诱导了它们之间的复合物形成。然而,使用小干扰RNA沉默p27Kip1或感染活性RhoA可阻断TM4SF5促进的G1/S期进程。对ROCK的药理学抑制加速了未表达对照TM4SF5的细胞的G1/S期进程。总之,这些观察结果表明,TM4SF5通过促进CDK4/细胞周期蛋白D1进入细胞核来加速G1/S期进程,这可能由TM4SF5介导的通过胞质p27Kip1表达和Rho GTP酶活性的肌动蛋白重组所支持。

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