Kasher Paul R, De Vos Kurt J, Wharton Stephen B, Manser Catherine, Bennett Ellen J, Bingley Megan, Wood Jonathan D, Milner Roy, McDermott Christopher J, Miller Christopher C J, Shaw Pamela J, Grierson Andrew J
Academic Neurology Unit, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield, UK.
J Neurochem. 2009 Jul;110(1):34-44. doi: 10.1111/j.1471-4159.2009.06104.x. Epub 2009 Apr 22.
Mutations in spastin are the most common cause of hereditary spastic paraplegia (HSP) but the mechanisms by which mutant spastin induces disease are not clear. Spastin functions to regulate microtubule organisation, and because of the essential role of microtubules in axonal transport, this has led to the suggestion that defects in axonal transport may underlie at least part of the disease process in HSP. However, as yet there is no direct evidence to support this notion. Here we analysed axonal transport in a novel mouse model of spastin-induced HSP that involves a pathogenic splice site mutation, which leads to a loss of spastin protein. A mutation located within the same splice site has been previously described in HSP. Spastin mice develop gait abnormalities that correlate with phenotypes seen in HSP patients and also axonal swellings containing cytoskeletal proteins, mitochondria and the amyloid precursor protein (APP). Pathological analyses of human HSP cases caused by spastin mutations revealed the presence of similar axonal swellings. To determine whether mutant spastin influenced axonal transport we quantified transport of two cargoes, mitochondria and APP-containing membrane bound organelles, in neurons from mutant spastin and control mice, using time-lapse microscopy. We found that mutant spastin perturbs anterograde transport of both cargoes. In neurons with axonal swellings we found that the mitochondrial axonal transport defects were exacerbated; distal to axonal swellings both anterograde and retrograde transport were severely reduced. These results strongly support a direct role for defective axonal transport in the pathogenesis of HSP because of spastin mutation.
痉挛素突变是遗传性痉挛性截瘫(HSP)最常见的病因,但突变型痉挛素诱发疾病的机制尚不清楚。痉挛素的功能是调节微管组织,由于微管在轴突运输中起关键作用,这使人认为轴突运输缺陷可能至少是HSP疾病进程的部分原因。然而,目前尚无直接证据支持这一观点。在此,我们分析了一种由痉挛素诱导的HSP新型小鼠模型中的轴突运输,该模型涉及一个致病性剪接位点突变,导致痉挛素蛋白缺失。先前在HSP中已描述过位于同一剪接位点的突变。痉挛素小鼠出现步态异常,这与HSP患者的表型相关,还出现含有细胞骨架蛋白、线粒体和淀粉样前体蛋白(APP)的轴突肿胀。对由痉挛素突变引起的人类HSP病例的病理分析显示存在类似的轴突肿胀。为了确定突变型痉挛素是否影响轴突运输,我们使用延时显微镜对突变型痉挛素小鼠和对照小鼠神经元中的两种货物(线粒体和含APP的膜结合细胞器)的运输进行了定量分析。我们发现突变型痉挛素扰乱了这两种货物的顺向运输。在有轴突肿胀的神经元中,我们发现线粒体轴突运输缺陷加剧;在轴突肿胀远端,顺向和逆向运输均严重减少。这些结果有力地支持了轴突运输缺陷在由痉挛素突变引起的HSP发病机制中起直接作用。