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肌萎缩侧索硬化症相关超氧化物歧化酶1(SOD1)突变体对动力蛋白和驱动蛋白5介导的轴突逆行和顺行运输的影响。

Effects of ALS-related SOD1 mutants on dynein- and KIF5-mediated retrograde and anterograde axonal transport.

作者信息

Shi Ping, Ström Anna-Lena, Gal Jozsef, Zhu Haining

机构信息

Department of Molecular and Cellular Biochemistry, College of Medicine, University of Kentucky, Lexington, KY 40536, USA.

出版信息

Biochim Biophys Acta. 2010 Sep;1802(9):707-16. doi: 10.1016/j.bbadis.2010.05.008. Epub 2010 May 25.

Abstract

Transport of material and signals between extensive neuronal processes and the cell body is essential to neuronal physiology and survival. Slowing of axonal transport has been shown to occur before the onset of symptoms in amyotrophic lateral sclerosis (ALS). We have previously shown that several familial ALS-linked copper-zinc superoxide dismutase (SOD1) mutants (A4V, G85R, and G93A) interacted and colocalized with the retrograde dynein-dynactin motor complex in cultured cells and affected tissues of ALS mice. We also found that the interaction between mutant SOD1 and the dynein motor played a critical role in the formation of large inclusions containing mutant SOD1. In this study, we showed that, in contrast to the dynein situation, mutant SOD1 did not interact with anterograde transport motors of the kinesin-1 family (KIF5A, B and C). Using dynein and kinesin accumulation at the sciatic nerve ligation sites as a surrogate measurement of axonal transport, we also showed that dynein mediated retrograde transport was slower in G93A than in WT mice at an early presymptomatic stage. While no decrease in KIF5A-mediated anterograde transport was detected, the slowing of anterograde transport of dynein heavy chain as a cargo was observed in the presymptomatic G93A mice. The results from this study along with other recently published work support that mutant SOD1 might only interact with and interfere with some kinesin members, which, in turn, could result in the impairment of a selective subset of cargos. Although it remains to be further investigated how mutant SOD1 affects different axonal transport motor proteins and various cargos, it is evident that mutant SOD1 can induce defects in axonal transport, which, subsequently, contribute to the propagation of toxic effects and ultimately motor neuron death in ALS.

摘要

在广泛的神经元突起与细胞体之间进行物质和信号的运输对于神经元的生理功能和存活至关重要。在肌萎缩侧索硬化症(ALS)症状出现之前,轴突运输就已显示出减慢的情况。我们之前已经表明,几种与家族性ALS相关的铜锌超氧化物歧化酶(SOD1)突变体(A4V、G85R和G93A)在培养细胞和ALS小鼠的受影响组织中与逆行动力蛋白-动力蛋白激活蛋白运动复合体相互作用并共定位。我们还发现,突变型SOD1与动力蛋白运动之间的相互作用在含有突变型SOD1的大包涵体形成中起关键作用。在本研究中,我们表明,与动力蛋白的情况相反,突变型SOD1不与驱动蛋白-1家族(KIF5A、B和C)的顺行运输马达相互作用。利用坐骨神经结扎部位的动力蛋白和驱动蛋白积累作为轴突运输的替代测量指标,我们还表明,在症状出现前的早期阶段,G93A小鼠中动力蛋白介导的逆行运输比野生型小鼠慢。虽然未检测到KIF5A介导的顺行运输减少,但在症状出现前的G93A小鼠中观察到作为货物的动力蛋白重链顺行运输减慢。本研究结果以及其他最近发表的工作支持,突变型SOD1可能仅与某些驱动蛋白成员相互作用并干扰它们,这反过来可能导致特定货物子集的运输受损。尽管仍有待进一步研究突变型SOD1如何影响不同的轴突运输运动蛋白和各种货物,但很明显,突变型SOD1可诱导轴突运输缺陷,随后导致毒性作用的传播,并最终导致ALS中的运动神经元死亡。

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