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Reactive astrogliosis in the era of single-cell transcriptomics

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    0571183 - ÚEM 2024 RIV CH eng J - Journal Article
    Matúšová, Z. - Hol, E.M. - Pěkný, M. - Kubista, M. - Valihrach, Lukáš
    Reactive astrogliosis in the era of single-cell transcriptomics.
    Frontiers in Cellular Neuroscience. Roč. 17, april (2023), č. článku 1173200. E-ISSN 1662-5102
    R&D Projects: GA ČR(CZ) GA23-05327S; GA ČR(CZ) GA23-06269S; GA MŠMT(CZ) LX22NPO5107; GA MŠMT(CZ) ED1.1.00/02.0109
    Institutional support: RVO:68378041
    Keywords : reactive astrogliosis * astrocytes * cell populations * single-cell * RNA-seq * neuroinflammation * neurodegeneration * CNS diseases
    OECD category: Neurosciences (including psychophysiology
    Impact factor: 5.3, year: 2022
    Method of publishing: Open access
    https://www.frontiersin.org/articles/10.3389/fncel.2023.1173200/full

    Reactive astrogliosis is a reaction of astrocytes to disturbed homeostasis in the
    central nervous system (CNS), accompanied by changes in astrocyte numbers,
    morphology, and function. Reactive astrocytes are important in the onset
    and progression of many neuropathologies, such as neurotrauma, stroke, and
    neurodegenerative diseases. Single-cell transcriptomics has revealed remarkable
    heterogeneity of reactive astrocytes, indicating their multifaceted functions in
    a whole spectrum of neuropathologies, with important temporal and spatial
    resolution, both in the brain and in the spinal cord. Interestingly, transcriptomic
    signatures of reactive astrocytes partially overlap between neurological diseases,
    suggesting shared and unique gene expression patterns in response to individual
    neuropathologies. In the era of single-cell transcriptomics, the number of
    new datasets steeply increases, and they often benefit from comparisons and
    integration with previously published work. Here, we provide an overview
    of reactive astrocyte populations defined by single-cell or single-nucleus
    transcriptomics across multiple neuropathologies, attempting to facilitate the
    search for relevant reference points and to improve the interpretability of new
    datasets containing cells with signatures of reactive astrocytes.
    Permanent Link: https://hdl.handle.net/11104/0342471

     
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