Dulbecco Telethon Institute, Department of Biology, University of Rome Tor Vergata, Rome, Italy.
Cell Death Differ. 2010 Jul;17(7):1104-14. doi: 10.1038/cdd.2009.180. Epub 2009 Dec 4.
Caspases are a family of cysteinyl aspartate-specific proteases that are highly conserved in multicellular organisms and function as central regulators of apoptosis. A member of this family, caspase-3, has been identified as a key mediator of apoptosis in neuronal cells. Recent studies in snail, fly and rat suggest that caspase-3 also functions as a regulatory molecule in neurogenesis and synaptic activity. In this study, in addition to providing an overview of the mechanism of caspase-3 activation, we review genetic and pharmacological studies of apoptotic and nonapoptotic functions of caspase-3 and discuss the regulatory mechanism of caspase-3 for executing nonapoptotic functions in the central nervous system. Knowledge of biochemical pathway(s) for nonapoptotic activation and modulation of caspase-3 has potential implications for the understanding of synaptic failure in the pathophysiology of neurological disorders. Fine-tuning of caspase-3 lays down a new challenge in identifying pharmacological avenues for treatment of many neurological disorders.
Caspases 是一类半胱氨酸天冬氨酸特异性蛋白酶家族,在多细胞生物中高度保守,作为细胞凋亡的核心调节剂发挥作用。该家族的一个成员 caspase-3 已被确定为神经元细胞凋亡的关键介质。蜗牛、苍蝇和老鼠的最近研究表明,caspase-3 也作为神经发生和突触活性的调节分子发挥作用。在这项研究中,除了提供 caspase-3 激活机制的概述外,我们还回顾了 caspase-3 的凋亡和非凋亡功能的遗传和药理学研究,并讨论了 caspase-3 用于在中枢神经系统中执行非凋亡功能的调节机制。对非凋亡激活和 caspase-3 调节的生化途径的了解,可能有助于理解神经疾病病理生理学中突触功能障碍。caspase-3 的精细调节为确定许多神经疾病治疗的药理学途径提出了新的挑战。