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在过表达外周蛋白的神经元中神经丝蛋白的轴突运输缺陷。

Defective axonal transport of neurofilament proteins in neurons overexpressing peripherin.

作者信息

Millecamps Stéphanie, Robertson Janice, Lariviere Roxanne, Mallet Jacques, Julien Jean-Pierre

机构信息

Research Centre of Centre Hospitalier Universitaire de Québec, Department of Anatomy and Physiology of Laval University, Quebec, Canada.

出版信息

J Neurochem. 2006 Aug;98(3):926-38. doi: 10.1111/j.1471-4159.2006.03932.x. Epub 2006 Jun 19.

Abstract

Peripherin is a type III neuronal intermediate filament detected in motor neuron inclusions of amyotrophic lateral sclerosis (ALS) patients. We previously reported that overexpression of peripherin provokes late-onset motor neuron dysfunction in transgenic mice. Here, we show that peripherin overexpression slows down axonal transport of neurofilament (NF) proteins, and that the transport defect precedes by several months the appearance of axonal spheroids in adult mice. Defective NF transport by peripherin up-regulation was further confirmed with dorsal root ganglia (DRG) neurons cultured from peripherin transgenic embryos. Immunofluorescence microscopy and western blotting revealed that excess peripherin provokes reduction in levels of hyperphosphorylated NF-H species in DRG neurites. Similarly the transport of a green fluorescent protein (GFP)-tagged NF-M, delivered by means of a lentiviral construct, was impaired in DRG neurites overexpressing peripherin. These results demonstrate that peripherin overexpression can cause defective transport of type IV NF proteins, a phenomenon that may account for the progressive formation of ALS-like spheroids in axons.

摘要

外周蛋白是一种III型神经元中间丝,在肌萎缩侧索硬化症(ALS)患者的运动神经元包涵体中可检测到。我们之前报道过,外周蛋白的过度表达会在转基因小鼠中引发迟发性运动神经元功能障碍。在此,我们表明外周蛋白的过度表达会减缓神经丝(NF)蛋白的轴突运输,并且在成年小鼠中,这种运输缺陷比轴突球体的出现早几个月。从外周蛋白转基因胚胎培养的背根神经节(DRG)神经元进一步证实了外周蛋白上调导致的NF运输缺陷。免疫荧光显微镜和蛋白质印迹显示,过量的外周蛋白会导致DRG神经突中高磷酸化NF-H水平降低。同样,通过慢病毒构建体递送的绿色荧光蛋白(GFP)标记的NF-M在过度表达外周蛋白的DRG神经突中的运输也受到损害。这些结果表明,外周蛋白的过度表达会导致IV型NF蛋白的运输缺陷,这一现象可能解释了轴突中ALS样球体的逐渐形成。

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