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在疾病早期抑制集落刺激因子1受体可改善SCA1小鼠的运动功能障碍。

Inhibition of colony-stimulating factor 1 receptor early in disease ameliorates motor deficits in SCA1 mice.

作者信息

Qu Wenhui, Johnson Andrea, Kim Joo Hyun, Lukowicz Abigail, Svedberg Daniel, Cvetanovic Marija

机构信息

Department of Neuroscience, Institute for Translational Neuroscience, University of Minnesota, 2101 6th Street SE, Minneapolis, MN, 55455, USA.

出版信息

J Neuroinflammation. 2017 May 25;14(1):107. doi: 10.1186/s12974-017-0880-z.

Abstract

BACKGROUND

Polyglutamine (polyQ) expansion in the protein Ataxin-1 (ATXN1) causes spinocerebellar ataxia type 1 (SCA1), a fatal dominantly inherited neurodegenerative disease characterized by motor deficits, cerebellar neurodegeneration, and gliosis. Currently, there are no treatments available to delay or ameliorate SCA1. We have examined the effect of depleting microglia during the early stage of disease by using PLX, an inhibitor of colony-stimulating factor 1 receptor (CSFR1), on disease severity in a mouse model of SCA1.

METHODS

Transgenic mouse model of SCA1, ATXN1[82Q] mice, and wild-type littermate controls were treated with PLX from 3 weeks of age. The effects of PLX on microglial density, astrogliosis, motor behavior, atrophy, and gene expression of Purkinje neurons were examined at 3 months of age.

RESULTS

PLX treatment resulted in the elimination of 70-80% of microglia from the cerebellum of both wild-type and ATXN1[82Q] mice. Importantly, PLX ameliorated motor deficits in SCA1 mice. While we have not observed significant improvement in the atrophy or disease-associated gene expression changes in Purkinje neurons upon PLX treatment, we have detected reduced expression of pro-inflammatory cytokine tumor necrosis factor alpha (TNFα) and increase in the protein levels of wild-type ataxin-1 and post-synaptic density protein 95 (PSD95) that may help improve PN function.

CONCLUSIONS

A decrease in the number of microglia during an early stage of disease resulted in the amelioration of motor deficits in SCA1 mice.

摘要

背景

蛋白质ataxin-1(ATXN1)中的聚谷氨酰胺(polyQ)扩增导致1型脊髓小脑共济失调(SCA1),这是一种致命的常染色体显性遗传神经退行性疾病,其特征为运动功能障碍、小脑神经变性和胶质增生。目前,尚无可用的治疗方法来延缓或改善SCA1。我们通过使用集落刺激因子1受体(CSFR1)抑制剂PLX,研究了在疾病早期清除小胶质细胞对SCA1小鼠模型疾病严重程度的影响。

方法

从3周龄开始,用PLX处理SCA1转基因小鼠模型、ATXN1[82Q]小鼠和野生型同窝对照。在3月龄时检测PLX对小胶质细胞密度、星形胶质细胞增生、运动行为、萎缩以及浦肯野神经元基因表达的影响。

结果

PLX处理使野生型和ATXN1[82Q]小鼠小脑中70%-80%的小胶质细胞被清除。重要的是,PLX改善了SCA1小鼠的运动功能障碍。虽然我们未观察到PLX处理后浦肯野神经元萎缩或疾病相关基因表达变化有显著改善,但我们检测到促炎细胞因子肿瘤坏死因子α(TNFα)表达降低,野生型ataxin-1和突触后致密蛋白95(PSD95)的蛋白水平升高,这可能有助于改善浦肯野神经元功能。

结论

疾病早期小胶质细胞数量减少可改善SCA1小鼠的运动功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3ed/5445366/d4bda7af3566/12974_2017_880_Fig1_HTML.jpg

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