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Neuronal Autophagy and Neurodevelopmental Disorders

Neurodevelopmental disorders include a wide range of diseases such as autism spectrum disorders and mental retardation. Mutations in several genes that regulate neural development and synapse function have been identified in neurodevelopmental disorders. Interestingly, some affected genes and pathwa...

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Detalles Bibliográficos
Autores principales: Lee, Kyung-Min, Hwang, Su-Kyung, Lee, Jin-A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807000/
https://www.ncbi.nlm.nih.gov/pubmed/24167408
http://dx.doi.org/10.5607/en.2013.22.3.133
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author Lee, Kyung-Min
Hwang, Su-Kyung
Lee, Jin-A
author_facet Lee, Kyung-Min
Hwang, Su-Kyung
Lee, Jin-A
author_sort Lee, Kyung-Min
collection PubMed
description Neurodevelopmental disorders include a wide range of diseases such as autism spectrum disorders and mental retardation. Mutations in several genes that regulate neural development and synapse function have been identified in neurodevelopmental disorders. Interestingly, some affected genes and pathways in these diseases are associated with the autophagy pathway. Autophagy is a complex, bulky degradative process that involves the sequestration of cellular proteins, RNA, lipids, and cellular organelles into lysosomes. Despite recent progress in elucidating the genetics and molecular pathogenesis of these disorders, little is known about the pathogenic mechanisms and autophagy-related pathways involved in common neurodevelopmental disorders. Therefore, in this review, we focus on the current understanding of neuronal autophagy as well as recent findings on genetics and the roles of autophagy pathway in common neurodevelopmental disorders.
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spelling pubmed-38070002013-10-28 Neuronal Autophagy and Neurodevelopmental Disorders Lee, Kyung-Min Hwang, Su-Kyung Lee, Jin-A Exp Neurobiol Review Article Neurodevelopmental disorders include a wide range of diseases such as autism spectrum disorders and mental retardation. Mutations in several genes that regulate neural development and synapse function have been identified in neurodevelopmental disorders. Interestingly, some affected genes and pathways in these diseases are associated with the autophagy pathway. Autophagy is a complex, bulky degradative process that involves the sequestration of cellular proteins, RNA, lipids, and cellular organelles into lysosomes. Despite recent progress in elucidating the genetics and molecular pathogenesis of these disorders, little is known about the pathogenic mechanisms and autophagy-related pathways involved in common neurodevelopmental disorders. Therefore, in this review, we focus on the current understanding of neuronal autophagy as well as recent findings on genetics and the roles of autophagy pathway in common neurodevelopmental disorders. The Korean Society for Brain and Neural Science 2013-09 2013-09-30 /pmc/articles/PMC3807000/ /pubmed/24167408 http://dx.doi.org/10.5607/en.2013.22.3.133 Text en Copyright © Experimental Neurobiology 2013. 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
Lee, Kyung-Min
Hwang, Su-Kyung
Lee, Jin-A
Neuronal Autophagy and Neurodevelopmental Disorders
title Neuronal Autophagy and Neurodevelopmental Disorders
title_full Neuronal Autophagy and Neurodevelopmental Disorders
title_fullStr Neuronal Autophagy and Neurodevelopmental Disorders
title_full_unstemmed Neuronal Autophagy and Neurodevelopmental Disorders
title_short Neuronal Autophagy and Neurodevelopmental Disorders
title_sort neuronal autophagy and neurodevelopmental disorders
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807000/
https://www.ncbi.nlm.nih.gov/pubmed/24167408
http://dx.doi.org/10.5607/en.2013.22.3.133
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