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空间转录组分析鉴定出一种与人类神经炎性斑块微环境相关的α表达星形胶质细胞状态。

Spatial Transcriptomic Analysis Identifies a -Expressing Astrocytic State Associated with the Human Neuritic Plaque Microenvironment.

作者信息

Karaahmet Berke, Zhang Ya, Duquesne Laurine, Sigalov Alina, Yung Christina, Kroshilina Alexandra, Bennett David A, Taga Mariko, Klein Hans-Ulrich

机构信息

Center for Translational & Computational Neuroimmunology, Department of Neurology and Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University Medical Center, New York, New York, USA.

Rush Alzheimer's Disease Center, Rush University Medical Center, Chicago, IL, USA.

出版信息

bioRxiv. 2024 Nov 14:2024.11.13.623438. doi: 10.1101/2024.11.13.623438.

DOI:10.1101/2024.11.13.623438
PMID:39605680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11601401/
Abstract

Single-nucleus transcriptomic studies have revealed glial cell states associated with Alzheimer's disease; however, these nuclei are dissociated from the complex architecture of the human neocortex. Here, we successfully performed an unbiased distance-based analytic strategy on spatially-registered transcriptomic data. Leveraging immunohistochemistry in the same tissue section, our analyses prioritized and other genes, such as metallothioneins, as altered in the vicinity of neuritic amyloid plaques. Results were validated at the protein level by immunofluorescence, highlighting that a reactive SERPINA3 astrocyte subtype, Ast.5, plays a role in the plaque microenvironment.

摘要

单核转录组学研究揭示了与阿尔茨海默病相关的神经胶质细胞状态;然而,这些细胞核与人类新皮质的复杂结构相分离。在这里,我们成功地对空间定位的转录组数据进行了无偏倚的基于距离的分析策略。利用同一组织切片中的免疫组织化学,我们的分析将 以及其他基因(如金属硫蛋白)确定为在神经炎性淀粉样斑块附近发生改变的基因。结果在蛋白质水平通过免疫荧光得到验证,突出显示一种反应性丝氨酸蛋白酶抑制剂 3 星形胶质细胞亚型 Ast.5 在斑块微环境中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b33/11601401/19859b3f9a0c/nihpp-2024.11.13.623438v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b33/11601401/deedc72ca4db/nihpp-2024.11.13.623438v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b33/11601401/80ba1eb353f0/nihpp-2024.11.13.623438v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b33/11601401/19859b3f9a0c/nihpp-2024.11.13.623438v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b33/11601401/deedc72ca4db/nihpp-2024.11.13.623438v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b33/11601401/80ba1eb353f0/nihpp-2024.11.13.623438v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b33/11601401/19859b3f9a0c/nihpp-2024.11.13.623438v1-f0003.jpg

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本文引用的文献

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SEA-AD is a multimodal cellular atlas and resource for Alzheimer's disease.SEA-AD是一个针对阿尔茨海默病的多模态细胞图谱和资源。
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Single-cell multiregion dissection of Alzheimer's disease.单细胞多区域剖析阿尔茨海默病。
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Single-cell genomics and regulatory networks for 388 human brains.单细胞基因组学和 388 个人类大脑的调控网络。
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Cerebrospinal fluid proteomics in patients with Alzheimer's disease reveals five molecular subtypes with distinct genetic risk profiles.阿尔茨海默病患者的脑脊液蛋白质组学研究揭示了具有不同遗传风险特征的五个分子亚型。
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