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少突胶质细胞是帕金森病病理过程的旁观者还是驱动者?

Are oligodendrocytes bystanders or drivers of Parkinson's disease pathology?

作者信息

Salazar Campos José María, Burbulla Lena F, Jäkel Sarah

机构信息

Metabolic Biochemistry, Biomedical Center (BMC), Faculty of Medicine, LMU Munich, Munich, Germany.

Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.

出版信息

PLoS Biol. 2025 Jan 8;23(1):e3002977. doi: 10.1371/journal.pbio.3002977. eCollection 2025 Jan.

DOI:10.1371/journal.pbio.3002977
PMID:39777410
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11709285/
Abstract

The major pathological feature of Parkinson 's disease (PD), the second most common neurodegenerative disease and most common movement disorder, is the predominant degeneration of dopaminergic neurons in the substantia nigra, a part of the midbrain. Despite decades of research, the molecular mechanisms of the origin of the disease remain unknown. While the disease was initially viewed as a purely neuronal disorder, results from single-cell transcriptomics have suggested that oligodendrocytes may play an important role in the early stages of Parkinson's. Although these findings are of high relevance, particularly to the search for effective disease-modifying therapies, the actual functional role of oligodendrocytes in Parkinson's disease remains highly speculative and requires a concerted scientific effort to be better understood. This Unsolved Mystery discusses the limited understanding of oligodendrocytes in PD, highlighting unresolved questions regarding functional changes in oligodendroglia, the role of myelin in nigral dopaminergic neurons, the impact of the toxic environment, and the aggregation of alpha-synuclein within oligodendrocytes.

摘要

帕金森病(PD)是第二常见的神经退行性疾病和最常见的运动障碍,其主要病理特征是中脑一部分黑质中多巴胺能神经元的显著退化。尽管经过数十年研究,该疾病起源的分子机制仍然未知。虽然该疾病最初被视为纯粹的神经元疾病,但单细胞转录组学的结果表明,少突胶质细胞可能在帕金森病的早期阶段发挥重要作用。尽管这些发现具有高度相关性,特别是对于寻找有效的疾病修饰疗法而言,但少突胶质细胞在帕金森病中的实际功能作用仍然高度推测性,需要共同的科学努力才能更好地理解。这一未解之谜讨论了对帕金森病中少突胶质细胞的有限理解,突出了关于少突胶质细胞功能变化、髓鞘在黑质多巴胺能神经元中的作用、有毒环境的影响以及少突胶质细胞内α-突触核蛋白聚集等未解决的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa30/11709285/5745aecb51cc/pbio.3002977.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa30/11709285/cdc94c4dda22/pbio.3002977.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa30/11709285/5745aecb51cc/pbio.3002977.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa30/11709285/cdc94c4dda22/pbio.3002977.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa30/11709285/5745aecb51cc/pbio.3002977.g002.jpg

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本文引用的文献

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snRNA-seq stratifies multiple sclerosis patients into distinct white matter glial responses.小核RNA测序将多发性硬化症患者分为不同的白质神经胶质反应类型。
Neuron. 2025 Feb 5;113(3):396-410.e9. doi: 10.1016/j.neuron.2024.11.016. Epub 2024 Dec 20.
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Molecular profiling of human substantia nigra identifies diverse neuron types associated with vulnerability in Parkinson's disease.人类黑质的分子剖析确定了与帕金森病易感性相关的多种神经元类型。
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Longitudinal modeling of human neuronal aging reveals the contribution of the RCAN1-TFEB pathway to Huntington's disease neurodegeneration.对人类神经元衰老的纵向建模揭示了 RCAN1-TFEB 通路对亨廷顿病神经退行性变的贡献。
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