VIB-KU Leuven Center for Brain& Disease Research, Leuven, Belgium
Department of Neurosciences, KU Leuven, Leuven, Belgium.
EMBO J. 2018 Sep 14;37(18). doi: 10.15252/embj.201898960. Epub 2018 Jul 31.
Parkinson's disease, the second most common neurodegenerative disorder, affects millions of people globally. There is no cure, and its prevalence will double by 2030. In recent years, numerous causative genes and risk factors for Parkinson's disease have been identified and more than half appear to function at the synapse. Subtle synaptic defects are thought to precede blunt neuronal death, but the mechanisms that are dysfunctional at synapses are only now being unraveled. Here, we review recent work and propose a model where different Parkinson proteins interact in a cell compartment-specific manner at the synapse where these proteins regulate endocytosis and autophagy. While this field is only recently emerging, the work suggests that the loss of synaptic homeostasis may contribute to neurodegeneration and is a key player in Parkinson's disease.
帕金森病是第二常见的神经退行性疾病,影响着全球数百万人。目前尚无治愈方法,其发病率到 2030 年将翻一番。近年来,已发现许多帕金森病的致病基因和风险因素,其中一半以上似乎在突触处发挥作用。人们认为,细微的突触缺陷可能先于神经元的迟钝死亡,但突触处功能失调的机制直到现在才被揭开。在这里,我们回顾了最近的工作,并提出了一个模型,即不同的帕金森蛋白以细胞区室特异性的方式在突触处相互作用,在突触处这些蛋白调节内吞作用和自噬。虽然这一领域直到最近才出现,但这项工作表明,突触稳态的丧失可能导致神经退行性变,是帕金森病的关键因素。