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Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease
Experimental evidence has demonstrated that several aspects of adult neural stem cells (NSCs), including their quiescence, proliferation, fate specification and differentiation, are regulated by epigenetic mechanisms. These control the expression of specific sets of genes, often including those enco...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080757/ https://www.ncbi.nlm.nih.gov/pubmed/24964731 http://dx.doi.org/10.1186/1750-1326-9-25 |
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author | Fitzsimons, Carlos P van Bodegraven, Emma Schouten, Marijn Lardenoije, Roy Kompotis, Konstantinos Kenis, Gunter van den Hurk, Mark Boks, Marco P Biojone, Caroline Joca, Samia Steinbusch, Harry WM Lunnon, Katie Mastroeni, Diego F Mill, Jonathan Lucassen, Paul J Coleman, Paul D van den Hove, Daniel LA Rutten, Bart PF |
author_facet | Fitzsimons, Carlos P van Bodegraven, Emma Schouten, Marijn Lardenoije, Roy Kompotis, Konstantinos Kenis, Gunter van den Hurk, Mark Boks, Marco P Biojone, Caroline Joca, Samia Steinbusch, Harry WM Lunnon, Katie Mastroeni, Diego F Mill, Jonathan Lucassen, Paul J Coleman, Paul D van den Hove, Daniel LA Rutten, Bart PF |
author_sort | Fitzsimons, Carlos P |
collection | PubMed |
description | Experimental evidence has demonstrated that several aspects of adult neural stem cells (NSCs), including their quiescence, proliferation, fate specification and differentiation, are regulated by epigenetic mechanisms. These control the expression of specific sets of genes, often including those encoding for small non-coding RNAs, indicating a complex interplay between various epigenetic factors and cellular functions. Previous studies had indicated that in addition to the neuropathology in Alzheimer’s disease (AD), plasticity-related changes are observed in brain areas with ongoing neurogenesis, like the hippocampus and subventricular zone. Given the role of stem cells e.g. in hippocampal functions like cognition, and given their potential for brain repair, we here review the epigenetic mechanisms relevant for NSCs and AD etiology. Understanding the molecular mechanisms involved in the epigenetic regulation of adult NSCs will advance our knowledge on the role of adult neurogenesis in degeneration and possibly regeneration in the AD brain. |
format | Online Article Text |
id | pubmed-4080757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40807572014-07-03 Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease Fitzsimons, Carlos P van Bodegraven, Emma Schouten, Marijn Lardenoije, Roy Kompotis, Konstantinos Kenis, Gunter van den Hurk, Mark Boks, Marco P Biojone, Caroline Joca, Samia Steinbusch, Harry WM Lunnon, Katie Mastroeni, Diego F Mill, Jonathan Lucassen, Paul J Coleman, Paul D van den Hove, Daniel LA Rutten, Bart PF Mol Neurodegener Review Experimental evidence has demonstrated that several aspects of adult neural stem cells (NSCs), including their quiescence, proliferation, fate specification and differentiation, are regulated by epigenetic mechanisms. These control the expression of specific sets of genes, often including those encoding for small non-coding RNAs, indicating a complex interplay between various epigenetic factors and cellular functions. Previous studies had indicated that in addition to the neuropathology in Alzheimer’s disease (AD), plasticity-related changes are observed in brain areas with ongoing neurogenesis, like the hippocampus and subventricular zone. Given the role of stem cells e.g. in hippocampal functions like cognition, and given their potential for brain repair, we here review the epigenetic mechanisms relevant for NSCs and AD etiology. Understanding the molecular mechanisms involved in the epigenetic regulation of adult NSCs will advance our knowledge on the role of adult neurogenesis in degeneration and possibly regeneration in the AD brain. BioMed Central 2014-06-25 /pmc/articles/PMC4080757/ /pubmed/24964731 http://dx.doi.org/10.1186/1750-1326-9-25 Text en Copyright © 2014 Fitzsimons et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Fitzsimons, Carlos P van Bodegraven, Emma Schouten, Marijn Lardenoije, Roy Kompotis, Konstantinos Kenis, Gunter van den Hurk, Mark Boks, Marco P Biojone, Caroline Joca, Samia Steinbusch, Harry WM Lunnon, Katie Mastroeni, Diego F Mill, Jonathan Lucassen, Paul J Coleman, Paul D van den Hove, Daniel LA Rutten, Bart PF Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease |
title | Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease |
title_full | Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease |
title_fullStr | Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease |
title_full_unstemmed | Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease |
title_short | Epigenetic regulation of adult neural stem cells: implications for Alzheimer’s disease |
title_sort | epigenetic regulation of adult neural stem cells: implications for alzheimer’s disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080757/ https://www.ncbi.nlm.nih.gov/pubmed/24964731 http://dx.doi.org/10.1186/1750-1326-9-25 |
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