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遗传性痉挛性截瘫:膜转运与运动通路。

Hereditary spastic paraplegias: membrane traffic and the motor pathway.

机构信息

Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, 9000 Rockville Pike, Bethesda, Maryland 20892, USA.

出版信息

Nat Rev Neurosci. 2011 Jan;12(1):31-42. doi: 10.1038/nrn2946.

Abstract

Voluntary movement is a fundamental way in which animals respond to, and interact with, their environment. In mammals, the main CNS pathway controlling voluntary movement is the corticospinal tract, which encompasses connections between the cerebral motor cortex and the spinal cord. Hereditary spastic paraplegias (HSPs) are a group of genetic disorders that lead to a length-dependent, distal axonopathy of fibres of the corticospinal tract, causing lower limb spasticity and weakness. Recent work aimed at elucidating the molecular cell biology underlying the HSPs has revealed the importance of basic cellular processes — especially membrane trafficking and organelle morphogenesis and distribution— in axonal maintenance and degeneration.

摘要

自愿运动是动物对环境做出反应和相互作用的一种基本方式。在哺乳动物中,控制自愿运动的主要中枢神经系统途径是皮质脊髓束,它包括大脑运动皮层和脊髓之间的连接。遗传性痉挛性截瘫(HSP)是一组遗传疾病,导致皮质脊髓束纤维的长度依赖性、远端轴索性神经病,引起下肢痉挛和无力。最近旨在阐明 HSP 基础分子细胞生物学的工作揭示了基本细胞过程的重要性——特别是膜运输和细胞器形态发生和分布——在轴突维持和退化中的作用。

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