帕金森病少突胶质细胞亚群的变化。

IF 3.3 3区 医学 Q2 NEUROSCIENCES
Eun-Jin Bae, Dayana Pérez-Acuña, Ka Hyun Rhee, Seung-Jae Lee
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引用次数: 0

摘要

帕金森病(PD)的特征是多巴胺能神经元的选择性丧失。虽然迄今为止对帕金森病的大多数研究都集中在神经元上,在一定程度上还集中在神经胶质上,但很少有研究研究少突胶质的变化。在这里,我们通过分析单核转录组,研究了帕金森病患者少突胶质细胞与对照组的异质性。这些分析揭示了PD患者中存在不同的少突胶质细胞群,表明分子特征存在相应的变化,特别是包括炎症反应的激活、对蛋白质折叠应激的反应和髓鞘形成异常。我们在一个α-突触核蛋白预制纤维注射的帕金森病小鼠模型中证实了髓鞘形成异常。这些结果表明,少突胶质细胞在帕金森病中获得了与疾病相关的表型,并可能导致伴随的神经退行性变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Changes in oligodendroglial subpopulations in Parkinson's disease.

Changes in oligodendroglial subpopulations in Parkinson's disease.

Parkinson's disease (PD) is characterized by a selective loss of dopaminergic neurons. While most research on PD conducted to date has focused on neurons and, to a certain extent, glia, few studies have investigated changes in oligodendroglia. Here, we investigated the heterogeneity of oligodendrocytes from PD patients compared with those of control cases by analyzing single-nuclei transcriptomes. These analyses revealed the presence of distinct oligodendrocyte populations in PD patients indicative of corresponding variations in molecular features, notably including activation of inflammatory responses, response to protein folding stress, and myelination abnormalities. We confirmed myelination abnormalities in an α-synuclein preformed fibril-injection mouse model of PD. These results suggest that oligodendrocytes acquire disease-associated phenotypes in PD and may contribute to the accompanying neurodegeneration.

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来源期刊
Molecular Brain
Molecular Brain NEUROSCIENCES-
CiteScore
7.30
自引率
0.00%
发文量
97
审稿时长
>12 weeks
期刊介绍: Molecular Brain is an open access, peer-reviewed journal that considers manuscripts on all aspects of studies on the nervous system at the molecular, cellular, and systems level providing a forum for scientists to communicate their findings. Molecular brain research is a rapidly expanding research field in which integrative approaches at the genetic, molecular, cellular and synaptic levels yield key information about the physiological and pathological brain. These studies involve the use of a wide range of modern techniques in molecular biology, genomics, proteomics, imaging and electrophysiology.
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