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Cell Fate Potential of NG2 Progenitors
Determining the origin of different glial subtypes is crucial to understand glial heterogeneity, and to enhance our knowledge of glial and progenitor cell behavior in embryos and adults. NG2-glia are homogenously distributed in a grid-like manner in both, gray and white matter of the adult brain. Wh...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303219/ https://www.ncbi.nlm.nih.gov/pubmed/32555386 http://dx.doi.org/10.1038/s41598-020-66753-9 |
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author | Sánchez-González, Rebeca Bribián, Ana López-Mascaraque, Laura |
author_facet | Sánchez-González, Rebeca Bribián, Ana López-Mascaraque, Laura |
author_sort | Sánchez-González, Rebeca |
collection | PubMed |
description | Determining the origin of different glial subtypes is crucial to understand glial heterogeneity, and to enhance our knowledge of glial and progenitor cell behavior in embryos and adults. NG2-glia are homogenously distributed in a grid-like manner in both, gray and white matter of the adult brain. While some NG2-glia in the CNS are responsible for the generation of mature oligodendrocytes (OPCs), most of them do not differentiate and they can proliferate outside of adult neurogenic niches. Thus, NG2-glia constitute a heterogeneous population containing different subpopulations with distinct functions. We hypothesized that their diversity emerges from specific progenitors during development, as occurs with other glial cell subtypes. To specifically target NG2-pallial progenitors and to define the NG2-glia lineage, as well as the NG2-progenitor potential, we designed two new StarTrack strategies using the NG2 promoter. These approaches label NG2 expressing progenitor cells, permitting the cell fates of these NG2 progenitors to be tracked in vivo. StarTrack labelled cells producing different neural phenotypes in different regions depending on the age targeted, and the strategy selected. This specific genetic targeting of neural progenitors in vivo has provided new data on the heterogeneous pool of NG2 progenitors at both embryonic and postnatal ages. |
format | Online Article Text |
id | pubmed-7303219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73032192020-06-22 Cell Fate Potential of NG2 Progenitors Sánchez-González, Rebeca Bribián, Ana López-Mascaraque, Laura Sci Rep Article Determining the origin of different glial subtypes is crucial to understand glial heterogeneity, and to enhance our knowledge of glial and progenitor cell behavior in embryos and adults. NG2-glia are homogenously distributed in a grid-like manner in both, gray and white matter of the adult brain. While some NG2-glia in the CNS are responsible for the generation of mature oligodendrocytes (OPCs), most of them do not differentiate and they can proliferate outside of adult neurogenic niches. Thus, NG2-glia constitute a heterogeneous population containing different subpopulations with distinct functions. We hypothesized that their diversity emerges from specific progenitors during development, as occurs with other glial cell subtypes. To specifically target NG2-pallial progenitors and to define the NG2-glia lineage, as well as the NG2-progenitor potential, we designed two new StarTrack strategies using the NG2 promoter. These approaches label NG2 expressing progenitor cells, permitting the cell fates of these NG2 progenitors to be tracked in vivo. StarTrack labelled cells producing different neural phenotypes in different regions depending on the age targeted, and the strategy selected. This specific genetic targeting of neural progenitors in vivo has provided new data on the heterogeneous pool of NG2 progenitors at both embryonic and postnatal ages. Nature Publishing Group UK 2020-06-18 /pmc/articles/PMC7303219/ /pubmed/32555386 http://dx.doi.org/10.1038/s41598-020-66753-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sánchez-González, Rebeca Bribián, Ana López-Mascaraque, Laura Cell Fate Potential of NG2 Progenitors |
title | Cell Fate Potential of NG2 Progenitors |
title_full | Cell Fate Potential of NG2 Progenitors |
title_fullStr | Cell Fate Potential of NG2 Progenitors |
title_full_unstemmed | Cell Fate Potential of NG2 Progenitors |
title_short | Cell Fate Potential of NG2 Progenitors |
title_sort | cell fate potential of ng2 progenitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303219/ https://www.ncbi.nlm.nih.gov/pubmed/32555386 http://dx.doi.org/10.1038/s41598-020-66753-9 |
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