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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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.
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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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