Department of Internal Medicine, University of Iowa, Iowa City, IA 52242, USA.
Neurobiol Dis. 2013 Jun;54:456-63. doi: 10.1016/j.nbd.2013.01.019. Epub 2013 Jan 30.
Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disorder caused by polyglutamine repeat expansions in Ataxin-1. Recent evidence supports a role for microRNAs (miRNAs) deregulation in SCA1 pathogenesis. However, the extent to which miRNAs may modulate the onset, progression or severity of SCA1 remains largely unknown. In this study, we used a mouse model of SCA1 to determine if miRNAs are misregulated in pre- and post-symptomatic SCA1 cerebellum. We found a significant alteration in the steady-state levels of numerous miRNAs prior to and following phenotypic onset. In addition, we provide evidence that increased miR-150 levels in SCA1 Purkinje neurons may modulate disease pathogenesis by targeting the expression of Rgs8 and Vegfa.
脊髓小脑共济失调 1 型(SCA1)是一种由 Ataxin-1 中的多聚谷氨酰胺重复扩展引起的显性遗传性神经退行性疾病。最近的证据支持 microRNAs(miRNAs)失调在 SCA1 发病机制中的作用。然而,miRNAs 调节 SCA1 的发病、进展或严重程度的程度在很大程度上尚不清楚。在这项研究中,我们使用 SCA1 的小鼠模型来确定 miRNA 是否在 SCA1 小脑的症状前和症状后失调。我们发现,在表型发作之前和之后,许多 miRNA 的稳态水平发生了显著改变。此外,我们提供的证据表明,SCA1 浦肯野神经元中 miR-150 水平的增加可能通过靶向 Rgs8 和 Vegfa 的表达来调节疾病的发病机制。