Ström Anna-Lena, Gal Jozsef, Shi Ping, Kasarskis Edward J, Hayward Lawrence J, Zhu Haining
Department of Molecular and Cellular Biochemistry, College of Medicine, University of Kentucky, Lexington, Kentucky, USA.
J Neurochem. 2008 Jul;106(2):495-505. doi: 10.1111/j.1471-4159.2008.05393.x. Epub 2008 Apr 1.
Transport of material between extensive neuronal processes and the cell body is crucial for neuronal function and survival. Growing evidence shows that deficits in axonal transport contribute to the pathogenesis of multiple neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). Here we review recent data indicating that defects in dynein-mediated retrograde axonal transport are involved in ALS etiology. We discuss how mutant copper-zinc superoxide dismutase (SOD1) and an aberrant interaction between mutant SOD1 and dynein could perturb retrograde transport of neurotrophic factors and mitochondria. A possible contribution of axonal transport to the aggregation and degradation processes of mutant SOD1 is also reviewed. We further consider how the interference with axonal transport and protein turnover by mutant SOD1 could influence the function and viability of motor neurons in ALS.
在广泛的神经元突起与细胞体之间进行物质运输对于神经元的功能和存活至关重要。越来越多的证据表明,轴突运输缺陷会导致包括肌萎缩侧索硬化症(ALS)在内的多种神经退行性疾病的发病机制。在此,我们综述了近期的数据,这些数据表明动力蛋白介导的逆行轴突运输缺陷与ALS病因有关。我们讨论了突变型铜锌超氧化物歧化酶(SOD1)以及突变型SOD1与动力蛋白之间的异常相互作用如何扰乱神经营养因子和线粒体的逆行运输。还综述了轴突运输对突变型SOD1聚集和降解过程的可能作用。我们进一步探讨了突变型SOD1对轴突运输和蛋白质周转的干扰如何影响ALS中运动神经元的功能和生存能力。