Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, China.
Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322.
Proc Natl Acad Sci U S A. 2020 Aug 18;117(33):20265-20273. doi: 10.1073/pnas.2002283117. Epub 2020 Aug 3.
Huntington disease (HD) is an ideal model for investigating selective neurodegeneration, as expanded polyQ repeats in the ubiquitously expressed huntingtin (HTT) cause the preferential neurodegeneration in the striatum of the HD patient brains. Here we report that adeno-associated virus (AAV) transduction-mediated depletion of Hap1, the first identified huntingtin-associated protein, in adult HD knock-in (KI) mouse brains leads to selective neuronal loss in the striatum. Further, Hap1 depletion-mediated neuronal loss via AAV transduction requires the presence of mutant HTT. Rhes, a GTPase that is enriched in the striatum and sumoylates mutant HTT to mediate neurotoxicity, binds more N-terminal HTT when Hap1 is deficient. Consistently, more soluble and sumoylated N-terminal HTT is presented in HD KI mouse striatum when HAP1 is absent. Our findings suggest that both Rhes and Hap1 as well as cellular stress contribute to the preferential neurodegeneration in HD, highlighting the involvement of multiple factors in selective neurodegeneration.
亨廷顿病(HD)是研究选择性神经退行性变的理想模型,因为在广泛表达的亨廷顿蛋白(HTT)中扩展的 polyQ 重复导致 HD 患者大脑纹状体中的选择性神经退行性变。在这里,我们报告说,腺相关病毒(AAV)转导介导的成年 HD 基因敲入(KI)小鼠大脑中第一个被鉴定的亨廷顿蛋白相关蛋白 Hap1 的耗竭导致纹状体中选择性神经元丢失。此外,通过 AAV 转导的 Hap1 耗竭介导的神经元丢失需要存在突变型 HTT。Rhes 是一种富含纹状体并通过 SUMOylation 介导神经毒性的 GTPase,当 Hap1 缺乏时,它与更多的 N 端 HTT 结合。一致地,当 HAP1 不存在时,HD KI 小鼠纹状体中存在更多的可溶性和 SUMOylated N 端 HTT。我们的发现表明,Rhes 和 Hap1 以及细胞应激都有助于 HD 中的选择性神经退行性变,突出了多种因素在选择性神经退行性变中的参与。