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多发性硬化症中的跨区域平衡和反应性神经胶质特征。

Cross-regional homeostatic and reactive glial signatures in multiple sclerosis.

机构信息

Division of Neuroimmunology, Department of Neurology, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Institute for Physiology and Pathophysiology, Heidelberg University, Heidelberg, Germany.

出版信息

Acta Neuropathol. 2022 Nov;144(5):987-1003. doi: 10.1007/s00401-022-02497-2. Epub 2022 Sep 16.

DOI:10.1007/s00401-022-02497-2
PMID:36112223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9547805/
Abstract

Multiple sclerosis (MS) is a multifocal and progressive inflammatory disease of the central nervous system (CNS). However, the compartmentalized pathology of the disease affecting various anatomical regions including gray and white matter and lack of appropriate disease models impede understanding of the disease. Utilizing single-nucleus RNA-sequencing and multiplex spatial RNA mapping, we generated an integrated transcriptomic map comprising leukocortical, cerebellar and spinal cord areas in normal and MS tissues that captures regional subtype diversity of various cell types with an emphasis on astrocytes and oligodendrocytes. While we found strong cross-regional diversity among glial subtypes in control tissue, regional signatures become more obscure in MS. This suggests that patterns of transcriptomic changes in MS are shared across regions and converge on specific pathways, especially those regulating cellular stress and immune activation. In addition, we found evidence that a subtype of white matter oligodendrocytes appearing across all three CNS regions adopt pro-remyelinating gene signatures in MS. In summary, our data suggest that cross-regional transcriptomic glial signatures overlap in MS, with different reactive glial cell types capable of either exacerbating or ameliorating pathology.

摘要

多发性硬化症(MS)是一种中枢神经系统(CNS)的多灶性、进行性炎症性疾病。然而,疾病的分隔病理学影响着包括灰质和白质在内的各种解剖区域,并且缺乏适当的疾病模型,这阻碍了对疾病的理解。利用单核 RNA 测序和多重空间 RNA 图谱分析,我们生成了一个整合的转录组图谱,包括正常和 MS 组织中的皮质白质、小脑和脊髓区域,该图谱捕获了各种细胞类型的区域亚型多样性,重点是星形胶质细胞和少突胶质细胞。虽然我们在对照组织中发现了胶质亚型之间存在强烈的跨区域多样性,但在 MS 中,区域特征变得更加模糊。这表明 MS 中转录组变化的模式在不同区域之间是共享的,并集中在特定的途径上,特别是那些调节细胞应激和免疫激活的途径。此外,我们发现证据表明,出现在所有三个 CNS 区域的一种白质少突胶质细胞亚型在 MS 中采用了促髓鞘形成的基因特征。总之,我们的数据表明,MS 中的跨区域转录组胶质特征存在重叠,不同的反应性胶质细胞类型能够加剧或减轻病理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/83fa1b1be5ab/401_2022_2497_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/41cdc9387f5c/401_2022_2497_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/4a6a79eecc1f/401_2022_2497_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/131aa184f817/401_2022_2497_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/83fa1b1be5ab/401_2022_2497_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/41cdc9387f5c/401_2022_2497_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/a83b3ad132b4/401_2022_2497_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/52ae29148b6e/401_2022_2497_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/4a6a79eecc1f/401_2022_2497_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/131aa184f817/401_2022_2497_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/9547805/83fa1b1be5ab/401_2022_2497_Fig6_HTML.jpg

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