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神经细胞周期失调与中枢神经系统疾病

Neural cell cycle dysregulation and central nervous system diseases.

作者信息

Wang Wei, Bu Bitao, Xie Minjie, Zhang Min, Yu Zhiyuan, Tao Deding

机构信息

Department of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, PR China.

出版信息

Prog Neurobiol. 2009 Sep;89(1):1-17. doi: 10.1016/j.pneurobio.2009.01.007. Epub 2009 Feb 4.

Abstract

The cell cycle is a delicately manipulated process essential for the development, differentiation, proliferation and death of cells. Inappropriate activation of cell cycle regulators is implicated in the pathophysiology of a wide range of central nervous system (CNS) diseases, including both acute damage and chronic neurodegenerative disorders. Cell cycle activation induces the dividing astrocytes and microglia to activate and proliferate in association with glial scar formation and inflammatory factor production, which play crucial roles in the development of pathology in CNS diseases. On the other hand, in terminally differentiated neurons, aberrant re-entry into the cell cycle triggers neuronal death instead of proliferation, which may be a common pathway shared by some acquired and neurodegenerative disorders, even though multiple pathways of the cell cycle machinery are involved in distinct neuronal demise in specific pathological circumstances. In this paper, we first provide a concise description of the roles of cell cycle in neural development. We then focus on how neural cell cycle dysregulation is related to CNS diseases. Neuronal apoptosis is often detected in acute injury to the CNS such as stroke and trauma, which are usually related to the blockade of the cell cycle at the G1-S phase. In neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis and Niemann-Pick disease type C, however, some populations of neurons complete DNA synthesis but the cell cycle is arrested at the G2/M transition. This review summarizes advances in findings implicating cell cycle machinery in neuronal death in CNS diseases.

摘要

细胞周期是一个受到精细调控的过程,对细胞的发育、分化、增殖和死亡至关重要。细胞周期调节因子的不适当激活与多种中枢神经系统(CNS)疾病的病理生理学相关,包括急性损伤和慢性神经退行性疾病。细胞周期激活诱导分裂的星形胶质细胞和小胶质细胞激活并增殖,同时伴有胶质瘢痕形成和炎症因子产生,这些在中枢神经系统疾病的病理发展中起关键作用。另一方面,在终末分化的神经元中,异常重新进入细胞周期会触发神经元死亡而非增殖,这可能是一些获得性和神经退行性疾病共有的常见途径,尽管细胞周期机制的多种途径在特定病理情况下参与不同的神经元死亡。在本文中,我们首先简要描述细胞周期在神经发育中的作用。然后我们关注神经细胞周期失调如何与中枢神经系统疾病相关。在中枢神经系统的急性损伤如中风和创伤中常检测到神经元凋亡,这通常与细胞周期在G1-S期的阻滞有关。然而,在神经退行性疾病如阿尔茨海默病、帕金森病、肌萎缩侧索硬化症和C型尼曼-匹克病中,一些神经元群体完成了DNA合成,但细胞周期在G2/M转换期停滞。本综述总结了有关细胞周期机制在中枢神经系统疾病神经元死亡中的研究进展。

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