Julien J P
Centre for Research in Neuroscience, Montreal General Hospital Research Institute, Canada.
Biochem Cell Biol. 1995 Sep-Oct;73(9-10):593-7. doi: 10.1139/o95-064.
Amyotrophic lateral sclerosis (ALS) is a late-onset degenerative disease of motor neurons, characterized by abnormal accumulation of neurofilaments (NFs) in perikarya and proximal axons. Two lines of evidence suggest that neurofilament accumulation can play a crucial role in ALS pathogenesis. First, transgenic mouse models overexpressing NF proteins were found to develop motor neuron degeneration and, second, variant alleles of the NF heavy-subunit (NF-H) gene have been found in some human ALS patients. Our axonal transport studies with transgenic mice overexpressing the human NF-H gene, a model of ALS, revealed defects of intracellular transport not only for neurofilament proteins but also for other cytoskeletal proteins and organelles such as mitochondria. Therefore, we propose that neurofilament accumulation in mice causes neurodegeneration by disrupting axonal transport, a mechanism that may account for the pathogenesis of ALS.
肌萎缩侧索硬化症(ALS)是一种运动神经元迟发性退行性疾病,其特征是神经丝(NFs)在神经元胞体和近端轴突中异常积聚。有两条证据表明神经丝积聚在ALS发病机制中可能起关键作用。第一,发现过表达NF蛋白的转基因小鼠模型会发生运动神经元变性;第二,在一些人类ALS患者中发现了NF重链亚基(NF-H)基因的变异等位基因。我们对过表达人类NF-H基因的转基因小鼠(一种ALS模型)进行的轴突运输研究表明,细胞内运输缺陷不仅存在于神经丝蛋白,还存在于其他细胞骨架蛋白和细胞器,如线粒体。因此,我们提出小鼠体内神经丝积聚通过破坏轴突运输导致神经变性,这一机制可能解释ALS的发病机制。