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帕金森病中α-突触核蛋白与小胶质细胞的关系:最新进展

The relation between α-synuclein and microglia in Parkinson's disease: Recent developments.

作者信息

Sanchez-Guajardo V, Tentillier N, Romero-Ramos M

机构信息

AU IDEAS center NEURODIN, Aarhus University, DK-8000 Aarhus C, Denmark; Neuroimmunology of Degenerative Disease, Department of Biomedicine, Aarhus University, DK-8000 Aarhus C, Denmark.

AU IDEAS center NEURODIN, Aarhus University, DK-8000 Aarhus C, Denmark; CNS Disease Modeling Group, Department of Biomedicine, Aarhus University, DK-8000 Aarhus C, Denmark.

出版信息

Neuroscience. 2015 Aug 27;302:47-58. doi: 10.1016/j.neuroscience.2015.02.008. Epub 2015 Feb 12.

Abstract

Recent research suggests a complex role for microglia not only in Parkinson's disease but in other disorders involving alpha-synuclein aggregation, such as multiple system atrophy. In these neurodegenerative processes, the activation of microglia is a common pathological finding, which disturbs the homeostasis of the neuronal environment otherwise maintained, among others, by microglia. The term activation comprises any deviation from what otherwise is considered normal microglia status, including cellular abundance, morphology or protein expression. The microglial response during disease will sustain survival or otherwise promote cell degeneration. The novel concepts of alpha-synuclein being released and uptaken by neighboring cells, and their importance in disease progression, positions microglia as the main cell that can clear and handle alpha-synuclein efficiently. Microglia's behavior will therefore be a determinant on the disease's progression. For this reason we believe that the better understanding of microglia's response to alpha-synuclein pathological accumulation across brain areas and disease stages is essential to develop novel therapeutic tools for Parkinson's disease and other alpha-synucleinopathies. In this review we will revise the most recent findings and developments with regard to alpha-synuclein and microglia in Parkinson's disease.

摘要

最近的研究表明,小胶质细胞不仅在帕金森病中,而且在其他涉及α-突触核蛋白聚集的疾病,如多系统萎缩中,都发挥着复杂的作用。在这些神经退行性过程中,小胶质细胞的激活是一种常见的病理表现,它会破坏原本由小胶质细胞等维持的神经元环境的稳态。“激活”一词包括任何偏离正常小胶质细胞状态的情况,包括细胞数量、形态或蛋白质表达。疾病期间小胶质细胞的反应将维持细胞存活,否则会促进细胞退化。α-突触核蛋白被邻近细胞释放和摄取的新概念,以及它们在疾病进展中的重要性,使小胶质细胞成为能够有效清除和处理α-突触核蛋白的主要细胞。因此,小胶质细胞的行为将决定疾病的进展。出于这个原因,我们认为,更好地了解小胶质细胞对大脑区域和疾病阶段中α-突触核蛋白病理积累的反应,对于开发针对帕金森病和其他α-突触核蛋白病的新型治疗工具至关重要。在这篇综述中,我们将回顾帕金森病中关于α-突触核蛋白和小胶质细胞的最新发现和进展。

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