Number of the records: 1  

Recent advances in deciphering oligodendrocyte heterogeneity with single-cell transcriptomics

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    SYSNO ASEP0566908
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRecent advances in deciphering oligodendrocyte heterogeneity with single-cell transcriptomics
    Author(s) Valihrach, Lukáš (UEM-P)
    Matúšová, Z. (CZ)
    Žucha, D. (CZ)
    Klassen, R. (CZ)
    Benešová, Š. (CZ)
    Abaffy, P. (CZ)
    Kubista, M. (CZ)
    Anděrová, Miroslava (UEM-P) RID, ORCID
    Article number1025012
    Source TitleFrontiers in Cellular Neuroscience. - : Frontiers Media
    Roč. 16, oct. (2022)
    Number of pages8 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsoligodendrocyte ; heterogeneity ; scRNA-seq ; snRNA-seq ; populations ; marker genes
    OECD categoryNeurosciences (including psychophysiology
    R&D ProjectsLX22NPO5107 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUEM-P - RVO:68378041
    UT WOS000875842100001
    EID SCOPUS85140777633
    DOI10.3389/fncel.2022.1025012
    AnnotationOligodendrocytes (OL) have been for decades considered a passive, homogenous population of cells that provide support to neurons, and show a limited response to pathological stimuli. This view has been dramatically changed by the introduction of powerful transcriptomic methods that have uncovered a broad spectrum of OL populations that co-exist within the healthy central nervous system (CNS) and also across a variety of diseases. Specifically, single-cell and single-nucleus RNA-sequencing (scRNA-seq, snRNA-seq) have been used to reveal OL variations in maturation, myelination and immune status. The newly discovered immunomodulatory role suggests that OL may serve as targets for future therapies. In this review, we summarize the current understanding of OL heterogeneity in mammalian CNS as revealed by scRNA-seq and snRNA-seq. We provide a list of key studies that identify consensus marker genes defining the currently known OL populations. This resource can be used to standardize analysis of OL related datasets and improve their interpretation, ultimately leading to a better understanding of OL functions in health and disease.
    WorkplaceInstitute of Experimental Medicine
    ContactLenka Koželská, lenka.kozelska@iem.cas.cz, Tel.: 241 062 218, 296 442 218
    Year of Publishing2023
    Electronic addresshttps://www.frontiersin.org/articles/10.3389/fncel.2022.1025012/full
Number of the records: 1  

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