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Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition

Critical periods (CP) in early post‐natal life are periods of plasticity during which the neuronal circuitry is most receptive to environmental stimuli. These early experiences translate to a more permanent and sophisticated neuronal connection in the adult brain systems. Multiple studies have point...

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Detalles Bibliográficos
Autores principales: Begum, M. Ridzwana, Sng, Judy C. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599941/
https://www.ncbi.nlm.nih.gov/pubmed/28628196
http://dx.doi.org/10.1111/jnc.14103
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author Begum, M. Ridzwana
Sng, Judy C. G.
author_facet Begum, M. Ridzwana
Sng, Judy C. G.
author_sort Begum, M. Ridzwana
collection PubMed
description Critical periods (CP) in early post‐natal life are periods of plasticity during which the neuronal circuitry is most receptive to environmental stimuli. These early experiences translate to a more permanent and sophisticated neuronal connection in the adult brain systems. Multiple studies have pointed to the development of inhibitory circuitry as one of the central factors for the onset of critical periods. We discuss several molecular mechanisms regulating inhibitory circuit maturation and CP, from gene transcription level to protein signaling level. Also, beyond the level of gene sequences, we briefly consider recent information on dynamic epigenetic regulation of gene expression through histone methylation and acetylation and their implication on timed development of the inhibitory circuitry for the onset of CP. [Image: see text]
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spelling pubmed-55999412017-10-02 Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition Begum, M. Ridzwana Sng, Judy C. G. J Neurochem Review Articles Critical periods (CP) in early post‐natal life are periods of plasticity during which the neuronal circuitry is most receptive to environmental stimuli. These early experiences translate to a more permanent and sophisticated neuronal connection in the adult brain systems. Multiple studies have pointed to the development of inhibitory circuitry as one of the central factors for the onset of critical periods. We discuss several molecular mechanisms regulating inhibitory circuit maturation and CP, from gene transcription level to protein signaling level. Also, beyond the level of gene sequences, we briefly consider recent information on dynamic epigenetic regulation of gene expression through histone methylation and acetylation and their implication on timed development of the inhibitory circuitry for the onset of CP. [Image: see text] John Wiley and Sons Inc. 2017-07-11 2017-09 /pmc/articles/PMC5599941/ /pubmed/28628196 http://dx.doi.org/10.1111/jnc.14103 Text en © 2017 The Authors. Journal of Neurochemistry published by John Wiley & Sons Ltd on behalf of International Society for Neurochemistry This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Begum, M. Ridzwana
Sng, Judy C. G.
Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition
title Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition
title_full Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition
title_fullStr Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition
title_full_unstemmed Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition
title_short Molecular mechanisms of experience‐dependent maturation in cortical GABAergic inhibition
title_sort molecular mechanisms of experience‐dependent maturation in cortical gabaergic inhibition
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599941/
https://www.ncbi.nlm.nih.gov/pubmed/28628196
http://dx.doi.org/10.1111/jnc.14103
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