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生长停滞和DNA损伤诱导基因153(GADD153)在血管平滑肌细胞凋亡中的作用。

Role of GADD153 (growth arrest- and DNA damage-inducible gene 153) in vascular smooth muscle cell apoptosis.

作者信息

Igase M, Okura T, Nakamura M, Takata Y, Kitami Y, Hiwada K

机构信息

Second Department of Internal Medicine, Ehime University School of Medicine, Onsen-gun, Ehime 791-0295, Japan.

出版信息

Clin Sci (Lond). 2001 Mar;100(3):275-81.

Abstract

GADD153 (growth arrest- and DNA damage-inducible gene 153) is expressed at very low levels in growing cells, but is markedly induced in response to a variety of cellular stresses, including glucose deprivation, exposure to genotoxic agents and other growth-arresting situations. Forced expression of GADD153 induces cell cycle arrest in many types of cells. It is also reported that GADD153 is directly associated with apoptosis. Recently we have reported that platelet-derived growth factor (PDGF)-BB induces apoptosis in cultured vascular smooth muscle cells (VSMC), but only when 100% confluency is reached. These results suggested that cell-cell contact inhibition (cell growth arrest) may be a critical factor for induction of VSMC apoptosis by PDGF-BB. In the present study, we explored the role of GADD153, one of a number of growth-arrest-related gene products, in the molecular mechanisms of VSMC apoptosis in vitro and in vivo. GADD153 was markedly induced at both the mRNA and protein levels, in parallel with the induction of VSMC apoptosis, after treatment with PDGF-BB. Moreover, overexpression of GADD153 in VSMC significantly reduced cell viability and induced apoptosis. In the carotid artery balloon injury model in rats, GADD153 protein was expressed in apoptotic VSMC which were positively stained by in situ DNA labelling. These results demonstrate an important role for GADD153 in the molecular mechanisms of VSMC apoptosis.

摘要

生长停滞和DNA损伤诱导基因153(GADD153)在生长的细胞中表达水平极低,但在受到多种细胞应激时会显著诱导表达,这些应激包括葡萄糖剥夺、接触基因毒性试剂以及其他生长停滞情况。在多种类型的细胞中,强制表达GADD153会诱导细胞周期停滞。也有报道称GADD153与细胞凋亡直接相关。最近我们报道了血小板衍生生长因子(PDGF)-BB可诱导培养的血管平滑肌细胞(VSMC)凋亡,但仅在细胞达到100%汇合时才会发生。这些结果表明,细胞-细胞接触抑制(细胞生长停滞)可能是PDGF-BB诱导VSMC凋亡的关键因素。在本研究中,我们探讨了众多生长停滞相关基因产物之一的GADD153在体外和体内VSMC凋亡分子机制中的作用。用PDGF-BB处理后,GADD153在mRNA和蛋白质水平均显著诱导,与VSMC凋亡的诱导同时发生。此外,VSMC中GADD153的过表达显著降低细胞活力并诱导凋亡。在大鼠颈动脉球囊损伤模型中,原位DNA标记呈阳性的凋亡VSMC中表达了GADD153蛋白。这些结果证明了GADD153在VSMC凋亡分子机制中的重要作用。

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