Wong P C, Borchelt D R
Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Curr Opin Neurol. 1995 Aug;8(4):294-301. doi: 10.1097/00019052-199508000-00008.
A subset of pedigrees with dominant inheritance of familial amyotrophic lateral sclerosis have mutations in superoxide dismutase 1. Initial studies suggested that disease-linked mutations impaired superoxide dismutase 1 activity, which is consistent with the notion that disease results from increased oxidative injury. However, results of recent cell culture and transgenic studies demonstrate that mutant proteins retaining high levels of superoxide dismutase 1 activity cause motor neuron degeneration; elevating the level of wild-type superoxide dismutase 1 does not cause disease. These findings suggest that the familial amyotrophic lateral sclerosis phenotype may occur through other mechanisms that can now be explored in model systems.
一部分家族性肌萎缩侧索硬化呈显性遗传的谱系中,超氧化物歧化酶1存在突变。初步研究表明,与疾病相关的突变会损害超氧化物歧化酶1的活性,这与疾病由氧化损伤增加所致的观点一致。然而,最近细胞培养和转基因研究的结果表明,保留高水平超氧化物歧化酶1活性的突变蛋白会导致运动神经元变性;提高野生型超氧化物歧化酶1的水平不会引发疾病。这些发现表明,家族性肌萎缩侧索硬化的表型可能通过其他机制出现,现在可以在模型系统中对这些机制进行探索。