Chuang De-Maw, Hough Christopher, Senatorov Vladimir V
Molecular Neurobiology Section, Mood and Anxiety Disorders Program, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892-1363, USA.
Annu Rev Pharmacol Toxicol. 2005;45:269-90. doi: 10.1146/annurev.pharmtox.45.120403.095902.
Increasing evidence supports the notion that glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is a protein with multiple functions, including its surprising role in apoptosis. GAPDH is overexpressed and accumulates in the nucleus during apoptosis induced by a variety of insults in diverse cell types. Knockdown of GAPDH using an antisense strategy demonstrates its involvement in the apoptotic cascade in which GAPDH nuclear translocation appears essential. Knowledge concerning the mechanisms underlying GAPDH nuclear translocation and subsequent cell death is growing. Additional evidence suggests that GAPDH may be an intracellular sensor of oxidative stress during early apoptosis. Abnormal expression, nuclear accumulation, changes in physical properties, and loss of glycolytic activity of GAPDH have been found in cellular and transgenic models as well as postmortem tissues of several neurodegenerative diseases. The interaction of GAPDH with disease-related proteins as well as drugs used to treat these diseases suggests that it is a potential molecular target for drug development.
越来越多的证据支持这样一种观点,即甘油醛-3-磷酸脱氢酶(GAPDH)是一种具有多种功能的蛋白质,包括其在细胞凋亡中令人惊讶的作用。在多种细胞类型中,由各种损伤诱导的细胞凋亡过程中,GAPDH会过度表达并在细胞核中积累。使用反义策略敲低GAPDH表明其参与了凋亡级联反应,其中GAPDH核转位似乎至关重要。关于GAPDH核转位及随后细胞死亡的潜在机制的知识正在不断增加。更多证据表明,GAPDH可能是早期细胞凋亡过程中氧化应激的细胞内传感器。在多种神经退行性疾病的细胞和转基因模型以及死后组织中,已发现GAPDH的异常表达、核积累、物理性质变化以及糖酵解活性丧失。GAPDH与疾病相关蛋白以及用于治疗这些疾病的药物之间相互作用表明,它是药物开发的一个潜在分子靶点。