Recent advances in deciphering oligodendrocyte heterogeneity with single-cell transcriptomics
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F22%3A00563715" target="_blank" >RIV/68378041:_____/22:00563715 - isvavai.cz</a>
Alternative codes found
RIV/86652036:_____/22:00563715 RIV/68378041:_____/22:00566908
Result on the web
<a href="https://www.frontiersin.org/articles/10.3389/fncel.2022.1025012/full" target="_blank" >https://www.frontiersin.org/articles/10.3389/fncel.2022.1025012/full</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3389/fncel.2022.1025012" target="_blank" >10.3389/fncel.2022.1025012</a>
Alternative languages
Result language
angličtina
Original language name
Recent advances in deciphering oligodendrocyte heterogeneity with single-cell transcriptomics
Original language description
Oligodendrocytes (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.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30103 - Neurosciences (including psychophysiology)
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Frontiers in Cellular Neuroscience
ISSN
1662-5102
e-ISSN
1662-5102
Volume of the periodical
16
Issue of the periodical within the volume
OCT 13 2022
Country of publishing house
CH - SWITZERLAND
Number of pages
8
Pages from-to
1025012
UT code for WoS article
000875842100001
EID of the result in the Scopus database
2-s2.0-85140777633