Department of Anatomy and Cell Biology, University of Illinois at Chicago, 808 S. Wood St., Rm 578 (M/C 512), Chicago, IL 60612, USA.
Mol Neurobiol. 2010 Aug;42(1):25-31. doi: 10.1007/s12035-010-8128-2. Epub 2010 May 18.
Although neuronal cell death through apoptotic pathways represents a common feature of dysferopathies, the canonical apoptotic changes familiar from nonneuronal cells are late events. Loss of neuronal function occurs at a much early time, when synaptic-based neuronal connectivity fails. In this context, apoptotic pathways may normally serve a cleanup role, rather than a pathogenic one. Reframing the consideration of cell death in the nervous system to include the early stages of axonal degeneration provides a better understanding of the roles played by various apoptotic signaling pathways in neurodegenerative diseases. Focusing on disease-specific mechanisms that initiate the sequence that eventually leads to neuronal loss should facilitate development of therapies that preserve neuronal function and neuronal numbers.
虽然通过细胞凋亡途径导致的神经元死亡是肌营养不良相关疾病的一个共同特征,但在熟悉的非神经元细胞中,典型的细胞凋亡变化是晚期事件。当基于突触的神经元连接失败时,神经元功能丧失发生得更早。在这种情况下,细胞凋亡途径可能正常发挥清除作用,而不是致病作用。将神经细胞死亡的考虑重新定义为包括轴突退化的早期阶段,可以更好地理解各种细胞凋亡信号通路在神经退行性疾病中的作用。关注启动最终导致神经元丧失的序列的特定疾病机制,应该有助于开发能够维持神经元功能和数量的治疗方法。