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聚(rC)结合蛋白PCBP2的时空表达调节坐骨神经损伤后雪旺细胞的增殖。

Spatiotemporal Expression of Poly(rC)-Binding Protein PCBP2 Modulates Schwann Cell Proliferation After Sciatic Nerve Injury.

作者信息

Chen Zhigang, Zhang Weidong, Ni Li, Wang Genlin, Cao Yi, Wu Weijie, Sun Chi, Yuan Damin, Ni Haidan, Wang Youhua, Yang Huilin

机构信息

Department of Orthopaedic Surgery, The First Affiliated Hospital of Soochow University, 188 Shizi Street, Suzhou, 215006, Jiangsu, People's Republic of China.

Department of Orthopedic Surgery, The Affiliated Hai'an Hospital of Nantong University, 17 Zhongba Middle Road, Hai'an, 226600, Jiangsu, People's Republic of China.

出版信息

Cell Mol Neurobiol. 2016 Jul;36(5):725-35. doi: 10.1007/s10571-015-0253-z. Epub 2015 Aug 7.

Abstract

Poly(C)-binding proteins (PCBPs), also known as RNA-binding proteins, interact in a sequence-specific fashion with single-stranded poly(C). It was reported that PCBP2 contributed to gastric cancer proliferation and survival through miR-34a, and knockdown of PCBP2 inhibited glioma proliferation through inhibition of cell cycle progression. In addition, PCBP2 might play a critical role in the regulation of cortical neurons apoptosis induced by hypoxia or ischemia. Because of the essential role of PCBP2 in nervous system and cell growth, we investigated the spatiotemporal expression of PCBP2 in a rat sciatic nerve crush (SNC) model. We detected the upregulated expression of PCBP2 in Schwann cell after SNC. Besides, the peak expression of PCBP2 was in parallel with proliferation cell nuclear antigen. In vitro, we observed increased expression of PCBP2 during the process of TNF-α-induced Schwann cell proliferation. Specially, PCBP2-specific siRNA-transfected Schwann cell showed significantly decreased ability for proliferation. Together, all these data indicated that the change of PCBP2 protein expression was associated with Schwann cell proliferation after the trauma of the peripheral nervous system.

摘要

多聚(C)结合蛋白(PCBP),也被称为RNA结合蛋白,以序列特异性方式与单链多聚(C)相互作用。据报道,PCBP2通过miR-34a促进胃癌的增殖和存活,而敲低PCBP2则通过抑制细胞周期进程抑制神经胶质瘤的增殖。此外,PCBP2可能在缺氧或缺血诱导的皮质神经元凋亡调控中起关键作用。由于PCBP2在神经系统和细胞生长中的重要作用,我们在大鼠坐骨神经挤压(SNC)模型中研究了PCBP2的时空表达。我们检测到SNC后雪旺细胞中PCBP2表达上调。此外,PCBP2的峰值表达与增殖细胞核抗原平行。在体外,我们观察到在TNF-α诱导雪旺细胞增殖过程中PCBP2表达增加。特别地,转染PCBP2特异性siRNA的雪旺细胞显示出显著降低的增殖能力。总之,所有这些数据表明,外周神经系统创伤后PCBP2蛋白表达的变化与雪旺细胞增殖有关。

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