Chang Chu Hua, Lim Kah Leong, Foo Jia Nee
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
Interdisciplinary Graduate Programme (IGP-Neuroscience), Nanyang Technological University, Singapore, Singapore.
Front Cell Neurosci. 2024 Sep 5;18:1437144. doi: 10.3389/fncel.2024.1437144. eCollection 2024.
Synaptic Vesicle Glycoprotein 2C (SV2C), characterized by its selective expression in discrete brain regions such as the midbrain, has recently emerged as a promising player in Parkinson's Disease (PD) - a debilitating neurodegenerative disorder affecting millions worldwide. This review aims to consolidate our current understanding of SV2C's function, its involvement in PD pathogenesis, and to evaluate its potential as a therapeutic target. Integrating previous findings of SV2C, from genetics to molecular studies, and drawing on insights from the largest East Asian genome-wide association study that highlights as a novel risk factor for PD, we explore the potential pathways through which SV2C may influence the disease. Our discussion extends to the implications of SV2C's role in synaptic vesicle trafficking, neurotransmitter release, and α-synuclein homeostasis, thereby laying the groundwork for future investigations that could pave the way for novel therapeutic strategies in combating PD.
突触小泡糖蛋白2C(SV2C),其特点是在中脑等离散脑区有选择性表达,最近已成为帕金森病(PD)——一种影响全球数百万人的使人衰弱的神经退行性疾病——中一个有前景的研究对象。本综述旨在巩固我们目前对SV2C功能的理解,其在PD发病机制中的作用,并评估其作为治疗靶点的潜力。整合先前关于SV2C的研究结果,从遗传学研究到分子研究,并借鉴最大规模的东亚全基因组关联研究的见解,该研究强调SV2C是PD的一个新风险因素,我们探索SV2C可能影响该疾病的潜在途径。我们的讨论扩展到SV2C在突触小泡运输、神经递质释放和α-突触核蛋白稳态中的作用的意义,从而为未来的研究奠定基础,这些研究可能为对抗PD的新治疗策略铺平道路。