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Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application
BACKGROUND: The transcriptional control of neuronal specification and early development has been intensively stud-ied over the past few decades. However, relatively little is known about transcriptional programs associated with the mainte-nance of terminally differentiated neuronal cells with respec...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883374/ https://www.ncbi.nlm.nih.gov/pubmed/28571546 http://dx.doi.org/10.2174/1570159X15666170601124220 |
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author | Lee, Jang Ho Kim, Jeong-Hoon Kim, Sunhong Cho, Kyoung Sang Lee, Sung Bae |
author_facet | Lee, Jang Ho Kim, Jeong-Hoon Kim, Sunhong Cho, Kyoung Sang Lee, Sung Bae |
author_sort | Lee, Jang Ho |
collection | PubMed |
description | BACKGROUND: The transcriptional control of neuronal specification and early development has been intensively stud-ied over the past few decades. However, relatively little is known about transcriptional programs associated with the mainte-nance of terminally differentiated neuronal cells with respect to their functions, structures, and cell type-specific identity features. METHODS: Notably, largely because of the recent advances in related techniques such as next generation sequencing and chromatin immunoprecipitation sequencing, the physiological implications of system-wide regulation of gene expression through changes in chromatin states have begun to be extensively studied in various contexts and systems, including the nervous system. RESULTS: Here, we attempt to review our current understanding of the link between chromatin changes and neuronal mainte-nance in the period of life after the completion of neuronal development. Perturbations involving chromatin changes in the system-wide transcriptional control are believed to be closely associated with diverse aspects of neuronal aging and neuro-degenerative conditions. CONCLUSION: In this review, we focused on heterochromatin and epigenetic dysregulation in neurodegenerative conditions as well as neuronal aging, the most important risk factor leading to neuronal degeneration, in order to highlight the close association between chromatin changes and neuronal maintenance. Lastly, we reviewed the cur-rently available and potential future applications of pharmacological control of the chromatin states associated with neuronal maintenance. |
format | Online Article Text |
id | pubmed-5883374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-58833742018-08-01 Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application Lee, Jang Ho Kim, Jeong-Hoon Kim, Sunhong Cho, Kyoung Sang Lee, Sung Bae Curr Neuropharmacol Article BACKGROUND: The transcriptional control of neuronal specification and early development has been intensively stud-ied over the past few decades. However, relatively little is known about transcriptional programs associated with the mainte-nance of terminally differentiated neuronal cells with respect to their functions, structures, and cell type-specific identity features. METHODS: Notably, largely because of the recent advances in related techniques such as next generation sequencing and chromatin immunoprecipitation sequencing, the physiological implications of system-wide regulation of gene expression through changes in chromatin states have begun to be extensively studied in various contexts and systems, including the nervous system. RESULTS: Here, we attempt to review our current understanding of the link between chromatin changes and neuronal mainte-nance in the period of life after the completion of neuronal development. Perturbations involving chromatin changes in the system-wide transcriptional control are believed to be closely associated with diverse aspects of neuronal aging and neuro-degenerative conditions. CONCLUSION: In this review, we focused on heterochromatin and epigenetic dysregulation in neurodegenerative conditions as well as neuronal aging, the most important risk factor leading to neuronal degeneration, in order to highlight the close association between chromatin changes and neuronal maintenance. Lastly, we reviewed the cur-rently available and potential future applications of pharmacological control of the chromatin states associated with neuronal maintenance. Bentham Science Publishers 2018-02 2018-02 /pmc/articles/PMC5883374/ /pubmed/28571546 http://dx.doi.org/10.2174/1570159X15666170601124220 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Lee, Jang Ho Kim, Jeong-Hoon Kim, Sunhong Cho, Kyoung Sang Lee, Sung Bae Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application |
title | Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application |
title_full | Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application |
title_fullStr | Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application |
title_full_unstemmed | Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application |
title_short | Chromatin Changes Associated with Neuronal Maintenance and Their Pharmacological Application |
title_sort | chromatin changes associated with neuronal maintenance and their pharmacological application |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883374/ https://www.ncbi.nlm.nih.gov/pubmed/28571546 http://dx.doi.org/10.2174/1570159X15666170601124220 |
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