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α-突触核蛋白丝氨酸 129 磷酸化的生理作用——并非矛盾。

Physiological roles of α-synuclein serine-129 phosphorylation - not an oxymoron.

机构信息

Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.

German Center for Neurodegenerative Diseases (DZNE) Munich, 81377 Munich, Germany; Chair of Metabolic Biochemistry, Biomedical Center (BMC), Faculty of Medicine, Ludwig-Maximilians-University, Munich, Germany; Munich Cluster for Systems Neurology (SyNergy), 81377 Munich, Germany.

出版信息

Trends Neurosci. 2024 Jul;47(7):480-490. doi: 10.1016/j.tins.2024.05.005. Epub 2024 Jun 10.

Abstract

α-Synuclein (αS) is an abundant presynaptic protein that regulates neurotransmission. It is also a key protein implicated in a broad class of neurodegenerative disorders termed synucleinopathies, including Parkinson's disease (PD) and Lewy body dementia (LBD). Pathological αS deposits in these diseases, Lewy bodies (LBs)/neurites (LNs), contain about 90% of αS in its phospho-serine129 (pS129) form. Therefore, pS129 is widely used as a surrogate marker of pathology. However, recent findings demonstrate that pS129 is also physiologically triggered by neuronal activity to positively regulate synaptic transmission. In this opinion article, we contrast the literature on pathological and physiological pS129, with a special focus on the latter. We emphasize that pS129 is ambiguous and knowledge about the context is necessary to correctly interpret changes in pS129.

摘要

α-突触核蛋白(αS)是一种丰富的突触前蛋白,它调节神经递质的释放。它也是一种关键蛋白,与广泛的神经退行性疾病类别有关,称为突触核蛋白病,包括帕金森病(PD)和路易体痴呆(LBD)。在这些疾病中,病理性的αS 沉积形成路易体(LB)/神经元纤维缠结(LN),其中约 90%的αS 以磷酸化丝氨酸 129 (pS129)的形式存在。因此,pS129 被广泛用作病理的替代标志物。然而,最近的发现表明,pS129 也被神经元活动生理性地触发,以积极调节突触传递。在这篇观点文章中,我们对比了病理性和生理性 pS129 的文献,特别关注后者。我们强调 pS129 是模糊的,并且需要了解上下文才能正确解释 pS129 的变化。

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