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Interplay between autophagy and programmed cell death in mammalian neural stem cells
Mammalian neural stem cells (NSCs) are of particular interest because of their role in brain development and function. Recent findings suggest the intimate involvement of programmed cell death (PCD) in the turnover of NSCs. However, the underlying mechanisms of PCD are largely unknown. Although apop...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society for Biochemistry and Molecular Biology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133905/ https://www.ncbi.nlm.nih.gov/pubmed/23977985 http://dx.doi.org/10.5483/BMBRep.2013.46.8.164 |
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author | Chung, Kyung Min Yu, Seong-Woon |
author_facet | Chung, Kyung Min Yu, Seong-Woon |
author_sort | Chung, Kyung Min |
collection | PubMed |
description | Mammalian neural stem cells (NSCs) are of particular interest because of their role in brain development and function. Recent findings suggest the intimate involvement of programmed cell death (PCD) in the turnover of NSCs. However, the underlying mechanisms of PCD are largely unknown. Although apoptosis is the best-defined form of PCD, accumulating evidence has revealed a wide spectrum of PCD encompassing apoptosis, autophagic cell death (ACD) and necrosis. This mini-review aims to illustrate a unique regulation of PCD in NSCs. The results of our recent studies on autophagic death of adult hippocampal neural stem (HCN) cells are also discussed. HCN cell death following insulin withdrawal clearly provides a reliable model that can be used to analyze the molecular mechanisms of ACD in the larger context of PCD. More research efforts are needed to increase our understanding of the molecular basis of NSC turnover under degenerating conditions, such as aging, stress and neurological diseases. Efforts aimed at protecting and harnessing endogenous NSCs will offer novel opportunities for the development of new therapeutic strategies for neuropathologies. [BMB Reports 2013; 46(8): 383-390] |
format | Online Article Text |
id | pubmed-4133905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41339052014-09-16 Interplay between autophagy and programmed cell death in mammalian neural stem cells Chung, Kyung Min Yu, Seong-Woon BMB Rep Review Article Mammalian neural stem cells (NSCs) are of particular interest because of their role in brain development and function. Recent findings suggest the intimate involvement of programmed cell death (PCD) in the turnover of NSCs. However, the underlying mechanisms of PCD are largely unknown. Although apoptosis is the best-defined form of PCD, accumulating evidence has revealed a wide spectrum of PCD encompassing apoptosis, autophagic cell death (ACD) and necrosis. This mini-review aims to illustrate a unique regulation of PCD in NSCs. The results of our recent studies on autophagic death of adult hippocampal neural stem (HCN) cells are also discussed. HCN cell death following insulin withdrawal clearly provides a reliable model that can be used to analyze the molecular mechanisms of ACD in the larger context of PCD. More research efforts are needed to increase our understanding of the molecular basis of NSC turnover under degenerating conditions, such as aging, stress and neurological diseases. Efforts aimed at protecting and harnessing endogenous NSCs will offer novel opportunities for the development of new therapeutic strategies for neuropathologies. [BMB Reports 2013; 46(8): 383-390] Korean Society for Biochemistry and Molecular Biology 2013-08 /pmc/articles/PMC4133905/ /pubmed/23977985 http://dx.doi.org/10.5483/BMBRep.2013.46.8.164 Text en Copyright © 2013, Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Chung, Kyung Min Yu, Seong-Woon Interplay between autophagy and programmed cell death in mammalian neural stem cells |
title | Interplay between autophagy and programmed cell death in mammalian neural stem cells |
title_full | Interplay between autophagy and programmed cell death in mammalian neural stem cells |
title_fullStr | Interplay between autophagy and programmed cell death in mammalian neural stem cells |
title_full_unstemmed | Interplay between autophagy and programmed cell death in mammalian neural stem cells |
title_short | Interplay between autophagy and programmed cell death in mammalian neural stem cells |
title_sort | interplay between autophagy and programmed cell death in mammalian neural stem cells |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133905/ https://www.ncbi.nlm.nih.gov/pubmed/23977985 http://dx.doi.org/10.5483/BMBRep.2013.46.8.164 |
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