Astrocyte transcriptomic changes along the spatiotemporal progression of Alzheimer’s disease

Astrocytes are crucial to brain homeostasis, yet their changes along the spatiotemporal progression of Alzheimer's disease (AD) neuropathology remain unexplored. Here we performed single-nucleus RNA sequencing of 628,943 astrocytes from five brain regions representing the stereotypical progression of AD pathology across 32 donors spanning the entire normal aging to severe AD continuum. We mapped out several unique astrocyte subclusters that exhibited varying responses to neuropathology across the AD-vulnerable neural network (spatial axis) or AD pathology stage (temporal axis). The proportion of homeostatic, intermediate and reactive astrocytes changed only along the spatial axis, whereas two other subclusters changed along the temporal axis. One of these, a trophic factor-rich subcluster, declined along pathology stages, whereas the other increased in the late stage but returned to baseline levels in the end stage, suggesting an exhausted response with chronic exposure to neuropathology. Our study underscores the complex dynamics of astrocytic responses in AD.

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Publication Details

Journal
Nature Neuroscience
Published
2024-11-11
DOI
https://doi.org/10.1038/s41593-024-01791-4
Citations
72
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
17.82

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article

Astrocyte transcriptomic changes along the spatiotemporal progression of Alzheimer’s disease

Eric Karran, Robert V. Talanian, Gen Lin, Taekyung Kwon et al.
72 citations
Nature Neuroscience
Neuroinflammation and Neurodegeneration Mechanisms
17.82
article

Astrocyte transcriptomic changes along the spatiotemporal progression of Alzheimer’s disease

Eric Karran, Robert V. Talanian, Gen Lin, Taekyung Kwon, Clara Muñoz‐Castro, Karen Zhao, Joseph A. Tamm, Ayush Noori, Zhaozhi Li, Rojashree Jayakumar, Alberto Serrano‐Pozo, Theresa R. Connors, Miwei Hu, Sudeshna Das, Timothy Pastika, Methasit Jaisa-aad, Bradley T. Hyman, Annie G. Bryant, Aicha Abdourahman, Maya E. Woodbury, Knut Biber, Rachel E. Bennett, Fan Liao, Huan Li, Astrid Wachter, Lindsay A Welikovitch, Molly A Healey
article en
72 citations

Abstract

Astrocytes are crucial to brain homeostasis, yet their changes along the spatiotemporal progression of Alzheimer's disease (AD) neuropathology remain unexplored. Here we performed single-nucleus RNA sequencing of 628,943 astrocytes from five brain regions representing the stereotypical progression of AD pathology across 32 donors spanning the entire normal aging to severe AD continuum. We mapped out several unique astrocyte subclusters that exhibited varying responses to neuropathology across the AD-vulnerable neural network (spatial axis) or AD pathology stage (temporal axis). The proportion of homeostatic, intermediate and reactive astrocytes changed only along the spatial axis, whereas two other subclusters changed along the temporal axis. One of these, a trophic factor-rich subcluster, declined along pathology stages, whereas the other increased in the late stage but returned to baseline levels in the end stage, suggesting an exhausted response with chronic exposure to neuropathology. Our study underscores the complex dynamics of astrocytic responses in AD.

Nature NeuroscienceVol. 27(12)
Harvard University (US), AbbVie (United States) (US), Massachusetts General Hospital (US), AbbVie (Germany) (DE), Klinikum Ludwigshafen (DE)
Alzheimer's Association, Harvard University, Massachusetts Life Sciences Center, Real Colegio Complutense, National Institutes of Health
Zero hunger
Openalex Percentile: Top 0%
Neuroinflammation and Neurodegeneration Mechanisms
17.82
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