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帕金森病中的α-突触核蛋白:从实验台到病床边

α-Synuclein in Parkinson's Disease: From Bench to Bedside.

作者信息

Bellini Gabriele, D'Antongiovanni Vanessa, Palermo Giovanni, Antonioli Luca, Fornai Matteo, Ceravolo Roberto, Bernardini Nunzia, Derkinderen Pascal, Pellegrini Carolina

机构信息

Center for Neurodegenerative Diseases, Unit of Neurology, Parkinson's Disease and Movement Disorders, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Department of Neurology, The Marlene and Paolo Fresco Institute for Parkinson's and Movement Disorders, NYU Langone Health, New York City, New York, USA.

出版信息

Med Res Rev. 2025 May;45(3):909-946. doi: 10.1002/med.22091. Epub 2024 Dec 20.

Abstract

α-Synuclein (α-syn), a pathological hallmark of PD, is emerging as a bridging element at the crossroads between neuro/immune-inflammatory responses and neurodegeneration in PD. Several evidence show that pathological α-syn accumulates in neuronal and non-neuronal cells (i.e., neurons, microglia, macrophages, skin cells, and intestinal cells) in central and peripheral tissues since the prodromal phase of the disease, contributing to brain pathology. Indeed, pathological α-syn deposition can promote neurogenic/immune-inflammatory responses that contribute to systemic and central neuroinflammation associated with PD. After providing an overview of the structure and functions of physiological α-syn as well as its pathological forms, we review current studies about the role of neuronal and non-neuronal α-syn at the crossroads between neuroinflammation and neurodegeneration in PD. In addition, we provide an overview of the correlation between the accumulation of α-syn in central and peripheral tissues and PD, related symptoms, and neuroinflammation. Special attention was paid to discussing whether targeting α-syn can represent a suitable therapeutical approach for PD.

摘要

α-突触核蛋白(α-syn)是帕金森病(PD)的一个病理标志,正成为PD神经/免疫炎症反应与神经退行性变之间交叉点上的一个桥梁元素。多项证据表明,自疾病前驱期起,病理性α-syn就在中枢和外周组织的神经元及非神经元细胞(即神经元、小胶质细胞、巨噬细胞、皮肤细胞和肠道细胞)中积累,从而导致脑部病变。事实上,病理性α-syn沉积可促进神经源性/免疫炎症反应,进而导致与PD相关的全身和中枢神经炎症。在概述了生理性α-syn的结构和功能及其病理形式之后,我们回顾了目前关于神经元和非神经元α-syn在PD神经炎症与神经退行性变交叉点上作用的研究。此外,我们还概述了α-syn在中枢和外周组织中的积累与PD、相关症状及神经炎症之间的相关性。特别关注了讨论靶向α-syn是否可能成为PD的一种合适治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db5/11976381/0b8ccc61489d/MED-45-909-g001.jpg

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