Ribe Elena M, Serrano-Saiz Esther, Akpan Nsikan, Troy Carol M
Department of Pathology, Taub Center for the Study of Alzheimer's Disease and the Aging Brain, Columbia University College of Physicians and Surgeons, 630 W. 168th Street, New York, NY 10032, USA.
Biochem J. 2008 Oct 15;415(2):165-82. doi: 10.1042/BJ20081118.
Dysregulation of life and death at the cellular level leads to a variety of diseases. In the nervous system, aberrant neuronal death is an outstanding feature of neurodegenerative diseases. Since the discovery of the caspase family of proteases, much effort has been made to determine how caspases function in disease, including neurodegenerative diseases. Although many papers have been published examining caspases in neuronal death and disease, the pathways have not been fully clarified. In the present review, we examine the potential players in the death pathways, the current tools for examining these players and the models for studying neurological disease. Alzheimer's disease, the most common neurodegenerative disorder, and cerebral ischaemia, the most common cause of neurological death, are used to illustrate our current understanding of death signalling in neurodegenerative diseases. A better understanding of the neuronal death pathways would provide targets for the development of therapeutic interventions for these diseases.
细胞水平上生死调节异常会导致多种疾病。在神经系统中,异常的神经元死亡是神经退行性疾病的一个突出特征。自蛋白酶半胱天冬酶家族被发现以来,人们付出了很多努力来确定半胱天冬酶在疾病(包括神经退行性疾病)中的作用方式。尽管已经发表了许多关于半胱天冬酶在神经元死亡和疾病中的研究论文,但相关途径尚未完全阐明。在本综述中,我们研究了死亡途径中的潜在参与者、用于研究这些参与者的当前工具以及用于研究神经疾病的模型。阿尔茨海默病(最常见的神经退行性疾病)和脑缺血(神经死亡的最常见原因)被用来阐述我们目前对神经退行性疾病中死亡信号的理解。更好地理解神经元死亡途径将为这些疾病的治疗干预开发提供靶点。