Dabool Lital, Hakim-Mishnaevski Ketty, Juravlev Liza, Flint-Brodsly Naama, Mandel Silvia, Kurant Estee
Department of Human Biology, Faculty of Natural Sciences, University of Haifa, 199 Aba Khoushy Avenue, Mount Carmel, Haifa 34988-38, Israel; The Rappaport Family Institute for Research in the Medical Sciences, Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Department of Human Biology, Faculty of Natural Sciences, University of Haifa, 199 Aba Khoushy Avenue, Mount Carmel, Haifa 34988-38, Israel.
iScience. 2020 Aug 21;23(8):101375. doi: 10.1016/j.isci.2020.101375. Epub 2020 Jul 16.
Skp1, a component of the ubiquitin E3 ligases, was found to be decreased in the brains of sporadic Parkinson's disease (PD) patients, and its overexpression prevented death of murine neurons in culture. Here we expose the neuroprotective role of the Drosophila skp1 homolog, skpA, in the adult brain. Neuronal knockdown of skpA leads to accumulation of ubiquitinated protein aggregates and loss of dopaminergic neurons accompanied by motor dysfunction and reduced lifespan. Conversely, neuronal overexpression of skpA reduces aggregate load, improves age-related motor decline, and prolongs lifespan. Moreover, SkpA rescues neurodegeneration in a Drosophila model of PD. We also show that a Drosophila homolog of FBXO7, the F Box protein, Nutcracker (Ntc), works in the same pathway with SkpA. However, skpA overexpression rescues ntc knockdown phenotype, suggesting that SkpA interacts with additional F box proteins in the adult brain neurons. Collectively, our study discloses Skp1/SkpA as a potential therapeutic target in neurodegenerative diseases.
Skp1是泛素E3连接酶的一个组成部分,在散发性帕金森病(PD)患者的大脑中被发现有所减少,其过表达可防止培养的小鼠神经元死亡。在此,我们揭示了果蝇skp1同源物skpA在成体大脑中的神经保护作用。对skpA进行神经元敲低会导致泛素化蛋白聚集体的积累以及多巴胺能神经元的丧失,并伴有运动功能障碍和寿命缩短。相反,skpA的神经元过表达可减少聚集体负荷,改善与年龄相关的运动衰退,并延长寿命。此外,SkpA可挽救PD果蝇模型中的神经退行性变。我们还表明,F盒蛋白Nutcracker(Ntc)的果蝇同源物与SkpA在同一途径中发挥作用。然而,skpA过表达可挽救ntc敲低的表型,这表明SkpA在成体大脑神经元中与其他F盒蛋白相互作用。总的来说,我们的研究揭示了Skp1/SkpA作为神经退行性疾病潜在治疗靶点的作用。