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组蛋白去乙酰化酶4(HDAC4)的上调与坐骨神经挤压后雪旺细胞增殖有关。

Up-regulation of HDAC4 is associated with Schwann cell proliferation after sciatic nerve crush.

作者信息

Liu Yonghua, Liu Yang, Nie Xiaoke, Cao Jianhua, Zhu Xiaojian, Zhang Weidong, Liu Zhongbing, Mao Xingxing, Yan Shixian, Ni Yingjie, Wang Youhua

机构信息

Department of Pathogen Biology, Medical College, Nantong University, Nantong, 226001, Jiangsu, People's Republic of China.

出版信息

Neurochem Res. 2014 Nov;39(11):2105-17. doi: 10.1007/s11064-014-1401-4. Epub 2014 Aug 8.

Abstract

Histone deacetylase 4 (HDAC4), a member of the class IIa HDACs subfamily, has emerged as a critical regulator of cell growth, differentiation, and migration in various cell types. It was reported that HDAC4 stimulated colon cell proliferation via repression of p21. Also, HDAC4 contributes to platelet-derived growth factor-BB-induced proliferation and migration of vascular smooth muscle cells. Furthermore, HDAC4 may play an important role in the regulation of neuronal differentiation and survival. However, the role of HDAC4 in the process of peripheral nervous system regeneration after injury remains virtually unknown. Herein, we investigated the spatiotemporal expression of HDAC4 in a rat sciatic nerve crush model. We found that sciatic nerve crush induced up-regulated expression of HDAC4 in Schwann cells. Moreover, the expression of the proliferation marker Ki-67 exhibited a similar tendency with that of HDAC4. In cell cultures, we observed increased expression of HDAC4 during the process of TNF-α-induced Schwann cell proliferation, whereas the protein level of p21 was down-regulated. Interference of HDAC4 led to enhanced expression of p21 and impaired proliferation of Schwan cells. Taken together, our findings implicated that HDAC4 was up-regulated in the sciatic nerve after crush, which was associated with proliferation of Schwann cells.

摘要

组蛋白去乙酰化酶4(HDAC4)是IIa类组蛋白去乙酰化酶亚家族的成员,已成为多种细胞类型中细胞生长、分化和迁移的关键调节因子。据报道,HDAC4通过抑制p21来刺激结肠细胞增殖。此外,HDAC4有助于血小板衍生生长因子-BB诱导的血管平滑肌细胞增殖和迁移。此外,HDAC4可能在神经元分化和存活的调节中起重要作用。然而,HDAC4在损伤后周围神经系统再生过程中的作用几乎仍不清楚。在此,我们在大鼠坐骨神经挤压模型中研究了HDAC4的时空表达。我们发现坐骨神经挤压诱导雪旺细胞中HDAC4的表达上调。此外,增殖标志物Ki-67的表达与HDAC4的表达呈现相似的趋势。在细胞培养中,我们观察到在TNF-α诱导雪旺细胞增殖的过程中HDAC4的表达增加,而p21的蛋白水平下调。干扰HDAC4导致p21的表达增强和雪旺细胞增殖受损。综上所述,我们的研究结果表明挤压后坐骨神经中HDAC4上调,这与雪旺细胞的增殖有关。

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