Sathasivam Sivakumar, Shaw Pamela J
The Walton Centre for Neurology and Neurosurgery, Liverpool, UK.
Lancet Neurol. 2005 Aug;4(8):500-9. doi: 10.1016/S1474-4422(05)70142-3.
There is increasing evidence that a programmed mechanism of cell death resembling apoptosis is responsible for motor-neuron degeneration in amyotrophic lateral sclerosis. Our understanding of the cell-death pathway has come from studies of both experimental models and human tissue. Here we examine in detail the in vitro and in vivo evidence for and against apoptosis in amyotrophic lateral sclerosis, looking at morphological changes, caspase activation, alterations in Bcl-2 oncoproteins, involvement of death receptors, expression of apoptosis-related molecules, and the role of the p53 pathway. Finally, we present evidence of potential therapeutic agents that could modulate the apoptotic pathway in amyotrophic lateral sclerosis and slow disease progression.
越来越多的证据表明,一种类似于凋亡的程序性细胞死亡机制是肌萎缩侧索硬化症中运动神经元变性的原因。我们对细胞死亡途径的理解来自于对实验模型和人体组织的研究。在这里,我们详细研究了支持和反对肌萎缩侧索硬化症中凋亡的体外和体内证据,观察形态学变化、半胱天冬酶激活、Bcl-2癌蛋白的改变、死亡受体的参与、凋亡相关分子的表达以及p53途径的作用。最后,我们展示了可能调节肌萎缩侧索硬化症中凋亡途径并减缓疾病进展的潜在治疗药物的证据。