Johnson E M, Deckwerth T L, Deshmukh M
Department of Neurology, Washington University School of Medicine, St. Louis MO 63110, USA.
Brain Pathol. 1996 Oct;6(4):397-409. doi: 10.1111/j.1750-3639.1996.tb00872.x.
Extensive neuronal death occurs in the developing nervous system. Death of neurons during this process is apoptotic and appears to utilize a pathway that is conserved in various mammalian cells and organisms. Recent evidence suggests that neuronal death during trauma, stroke, or neurodegenerative diseases may also occur by a similar mechanism. This review discusses the molecular mechanism of developmental neuronal death by examining the biochemical and molecular events associated with neuronal death after trophic factor withdrawal. The ability to inhibit neuronal death by manipulating the Bcl-2 or the ICE-family proteins demonstrates the importance of these proteins in the neuronal apoptotic pathway. The utility of inhibiting neuronal death by blocking the apoptotic pathway as therapy in neuropathological situations is discussed.
在发育中的神经系统中会发生广泛的神经元死亡。在此过程中神经元的死亡是凋亡性的,并且似乎利用了在各种哺乳动物细胞和生物体中保守的一条途径。最近的证据表明,创伤、中风或神经退行性疾病期间的神经元死亡也可能通过类似的机制发生。本综述通过研究与营养因子撤除后神经元死亡相关的生化和分子事件,探讨发育性神经元死亡的分子机制。通过操纵Bcl-2或ICE家族蛋白来抑制神经元死亡的能力证明了这些蛋白在神经元凋亡途径中的重要性。还讨论了在神经病理学情况下通过阻断凋亡途径来抑制神经元死亡作为治疗方法的实用性。