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Regulation of neural progenitor cell state by ephrin-B
Maintaining a balance between self-renewal and differentiation in neural progenitor cells during development is important to ensure that correct numbers of neural cells are generated. We report that the ephrin-B–PDZ-RGS3 signaling pathway functions to regulate this balance in the developing mammalia...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426945/ https://www.ncbi.nlm.nih.gov/pubmed/18541704 http://dx.doi.org/10.1083/jcb.200708091 |
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author | Qiu, Runxiang Wang, Xiuyun Davy, Alice Wu, Chen Murai, Kiyohito Zhang, Heying Flanagan, John G. Soriano, Philippe Lu, Qiang |
author_facet | Qiu, Runxiang Wang, Xiuyun Davy, Alice Wu, Chen Murai, Kiyohito Zhang, Heying Flanagan, John G. Soriano, Philippe Lu, Qiang |
author_sort | Qiu, Runxiang |
collection | PubMed |
description | Maintaining a balance between self-renewal and differentiation in neural progenitor cells during development is important to ensure that correct numbers of neural cells are generated. We report that the ephrin-B–PDZ-RGS3 signaling pathway functions to regulate this balance in the developing mammalian cerebral cortex. During cortical neurogenesis, expression of ephrin-B1 and PDZ-RGS3 is specifically seen in progenitor cells and is turned off at the onset of neuronal differentiation. Persistent expression of ephrin-B1 and PDZ-RGS3 prevents differentiation of neural progenitor cells. Blocking RGS-mediated ephrin-B1 signaling in progenitor cells through RNA interference or expression of dominant-negative mutants results in differentiation. Genetic knockout of ephrin-B1 causes early cell cycle exit and leads to a concomitant loss of neural progenitor cells. Our results indicate that ephrin-B function is critical for the maintenance of the neural progenitor cell state and that this role of ephrin-B is mediated by PDZ-RGS3, likely via interacting with the noncanonical G protein signaling pathway, which is essential in neural progenitor asymmetrical cell division. |
format | Text |
id | pubmed-2426945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24269452008-12-16 Regulation of neural progenitor cell state by ephrin-B Qiu, Runxiang Wang, Xiuyun Davy, Alice Wu, Chen Murai, Kiyohito Zhang, Heying Flanagan, John G. Soriano, Philippe Lu, Qiang J Cell Biol Research Articles Maintaining a balance between self-renewal and differentiation in neural progenitor cells during development is important to ensure that correct numbers of neural cells are generated. We report that the ephrin-B–PDZ-RGS3 signaling pathway functions to regulate this balance in the developing mammalian cerebral cortex. During cortical neurogenesis, expression of ephrin-B1 and PDZ-RGS3 is specifically seen in progenitor cells and is turned off at the onset of neuronal differentiation. Persistent expression of ephrin-B1 and PDZ-RGS3 prevents differentiation of neural progenitor cells. Blocking RGS-mediated ephrin-B1 signaling in progenitor cells through RNA interference or expression of dominant-negative mutants results in differentiation. Genetic knockout of ephrin-B1 causes early cell cycle exit and leads to a concomitant loss of neural progenitor cells. Our results indicate that ephrin-B function is critical for the maintenance of the neural progenitor cell state and that this role of ephrin-B is mediated by PDZ-RGS3, likely via interacting with the noncanonical G protein signaling pathway, which is essential in neural progenitor asymmetrical cell division. The Rockefeller University Press 2008-06-16 /pmc/articles/PMC2426945/ /pubmed/18541704 http://dx.doi.org/10.1083/jcb.200708091 Text en © 2008 Qiu et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Qiu, Runxiang Wang, Xiuyun Davy, Alice Wu, Chen Murai, Kiyohito Zhang, Heying Flanagan, John G. Soriano, Philippe Lu, Qiang Regulation of neural progenitor cell state by ephrin-B |
title | Regulation of neural progenitor cell state by ephrin-B |
title_full | Regulation of neural progenitor cell state by ephrin-B |
title_fullStr | Regulation of neural progenitor cell state by ephrin-B |
title_full_unstemmed | Regulation of neural progenitor cell state by ephrin-B |
title_short | Regulation of neural progenitor cell state by ephrin-B |
title_sort | regulation of neural progenitor cell state by ephrin-b |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426945/ https://www.ncbi.nlm.nih.gov/pubmed/18541704 http://dx.doi.org/10.1083/jcb.200708091 |
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