Novel Tools and Investigative Approaches for the Study of Oligodendrocyte Precursor Cells (NG2-Glia) in CNS Development and Disease.

NG2-glia genetic alteration heterogeneity imaging oligodendrocyte precursor cells sequencing

Journal

Frontiers in cellular neuroscience
ISSN: 1662-5102
Titre abrégé: Front Cell Neurosci
Pays: Switzerland
ID NLM: 101477935

Informations de publication

Date de publication:
2021
Historique:
received: 26 02 2021
accepted: 07 04 2021
entrez: 17 5 2021
pubmed: 18 5 2021
medline: 18 5 2021
Statut: epublish

Résumé

Oligodendrocyte progenitor cells (OPCs), also referred to as NG2-glia, are the most proliferative cell type in the adult central nervous system. While the primary role of OPCs is to serve as progenitors for oligodendrocytes, in recent years, it has become increasingly clear that OPCs fulfil a number of other functions. Indeed, independent of their role as stem cells, it is evident that OPCs can regulate the metabolic environment, directly interact with and modulate neuronal function, maintain the blood brain barrier (BBB) and regulate inflammation. In this review article, we discuss the state-of-the-art tools and investigative approaches being used to characterize the biology and function of OPCs. From functional genetic investigation to single cell sequencing and from lineage tracing to functional imaging, we discuss the important discoveries uncovered by these techniques, such as functional and spatial OPC heterogeneity, novel OPC marker genes, the interaction of OPCs with other cells types, and how OPCs integrate and respond to signals from neighboring cells. Finally, we review the use of

Identifiants

pubmed: 33994951
doi: 10.3389/fncel.2021.673132
pmc: PMC8116629
doi:

Types de publication

Journal Article

Langues

eng

Pagination

673132

Informations de copyright

Copyright © 2021 Galichet, Clayton and Lovell-Badge.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Christophe Galichet (C)

Laboratory of Stem Cell Biology and Developmental Genetics, The Francis Crick Institute, London, United Kingdom.

Richard W Clayton (RW)

Laboratory of Stem Cell Biology and Developmental Genetics, The Francis Crick Institute, London, United Kingdom.

Robin Lovell-Badge (R)

Laboratory of Stem Cell Biology and Developmental Genetics, The Francis Crick Institute, London, United Kingdom.

Classifications MeSH