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帕金森病中的突触蛋白稳态。

Synaptic proteostasis in Parkinson's disease.

机构信息

VIB Center for Brain & Disease Research, 3000 Leuven, Belgium; KU Leuven, Department of Neurosciences, Leuven Brain Institute, Mission Lucidity, Herestraat 49, Box 602, 3000 Leuven, Belgium.

VIB Center for Brain & Disease Research, 3000 Leuven, Belgium; KU Leuven, Department of Neurosciences, Leuven Brain Institute, Mission Lucidity, Herestraat 49, Box 602, 3000 Leuven, Belgium.

出版信息

Curr Opin Neurobiol. 2022 Feb;72:72-79. doi: 10.1016/j.conb.2021.09.001. Epub 2021 Oct 13.

Abstract

There are over 7 million people worldwide suffering from Parkinson's disease, and this number will double in the next decade. Causative mutations and risk variants in >20 genes that predominantly act at synapses have been linked to Parkinson's disease. Synaptic defects precede neuronal death. However, we are only now beginning to understand which molecular mechanisms contribute to this synaptic dysfunction. In this review, we discuss recent data demonstrating that Parkinson proteins act centrally to various protein quality control pathways at the synapse, and we argue that disturbed synaptic proteostasis is an early driver of neurodegeneration in Parkinson's disease.

摘要

全球有超过 700 万人患有帕金森病,这个数字在未来十年内将翻一番。 >20 个主要在突触处起作用的基因中的致病突变和风险变异与帕金森病有关。突触缺陷先于神经元死亡。然而,我们现在才开始了解哪些分子机制导致了这种突触功能障碍。在这篇综述中,我们讨论了最近的数据,这些数据表明帕金森蛋白在突触处集中作用于各种蛋白质质量控制途径,我们认为突触蛋白稳态紊乱是帕金森病神经退行性变的早期驱动因素。

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