Department of Genomic Medicine and Toxicology, Institute of Biomedical Research, National University of Mexico, Mexico City, Mexico.
Neurosci Bull. 2011 Jun;27(3):185-96. doi: 10.1007/s12264-011-1002-z.
Although the cell cycle machinery is essentially linked to cellular proliferation, recent findings suggest that neuronal cell death is frequently concurrent with the aberrant expression of cell cycle proteins in post-mitotic neurons. The present work reviews the evidence of cell cycle reentry and expression of cell cycle-associated proteins as a complex response of neurons to insults in the adult brain but also as a mechanism underlying brain plasticity. The basic aspects of cell cycle mechanisms, as well as the evidence showing cell cycle protein expression in the injured brain, are reviewed. The discussion includes recent experimental work attempting to establish a correlation between altered brain plasticity and neuronal death, and an analysis of recent evidence on how neural cell cycle dysregulation is related to neurodegenerative diseases especially the Alzheimer's disease. Understanding the mechanisms that control reexpression of proteins required for cell cycle progression which is involved in brain remodeling, may shed new light into the mechanisms involved in neuronal demise under diverse pathological circumstances. This would provide valuable clues about the possible therapeutic targets, leading to potential treatment of presently challenging neurodegenerative diseases.
尽管细胞周期机制本质上与细胞增殖相关,但最近的研究结果表明,细胞周期蛋白在有丝分裂后神经元中的异常表达与神经元细胞死亡经常同时发生。本研究综述了细胞周期重新进入和细胞周期相关蛋白表达的证据,认为这是成年大脑中神经元对损伤的一种复杂反应,但也是大脑可塑性的一种机制。本文综述了细胞周期机制的基本方面,以及在受损大脑中显示细胞周期蛋白表达的证据。讨论包括最近的实验工作,试图确定改变的大脑可塑性与神经元死亡之间的相关性,以及对神经细胞周期失调与神经退行性疾病(尤其是阿尔茨海默病)之间关系的最新证据的分析。了解控制细胞周期进展所需蛋白重新表达的机制,可能会为不同病理情况下神经元死亡的机制提供新的线索。这将为可能的治疗靶点提供有价值的线索,从而为目前具有挑战性的神经退行性疾病的治疗提供潜在的治疗方法。