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Zebrafish as a model to understand autophagy and its role in neurological disease()

In the past decade, the zebrafish (Danio rerio) has become a popular model system for the study of vertebrate development, since the embryos and larvae of this species are small, transparent and undergo rapid development ex utero, allowing in vivo analysis of embryogenesis and organogenesis. These c...

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Detalles Bibliográficos
Autores principales: Fleming, Angeleen, Rubinsztein, David C.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Pub. Co 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060341/
https://www.ncbi.nlm.nih.gov/pubmed/21256213
http://dx.doi.org/10.1016/j.bbadis.2011.01.004
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author Fleming, Angeleen
Rubinsztein, David C.
author_facet Fleming, Angeleen
Rubinsztein, David C.
author_sort Fleming, Angeleen
collection PubMed
description In the past decade, the zebrafish (Danio rerio) has become a popular model system for the study of vertebrate development, since the embryos and larvae of this species are small, transparent and undergo rapid development ex utero, allowing in vivo analysis of embryogenesis and organogenesis. These characteristics can also be exploited by researchers interested in signaling pathways and disease processes and, accordingly, there is a growing literature on the use of zebrafish to model human disease. This model holds great potential for exploring how autophagy, an evolutionarily conserved mechanism for protein degradation, influences the pathogeneses of a range of different human diseases and for the evaluation of this pathway as a potential therapeutic strategy. Here we summarize what is known about the regulation of autophagy in eukaryotic cells and its role in neurodegenerative disease and highlight how research using zebrafish has helped further our understanding of these processes.
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spelling pubmed-30603412011-04-12 Zebrafish as a model to understand autophagy and its role in neurological disease() Fleming, Angeleen Rubinsztein, David C. Biochim Biophys Acta Review In the past decade, the zebrafish (Danio rerio) has become a popular model system for the study of vertebrate development, since the embryos and larvae of this species are small, transparent and undergo rapid development ex utero, allowing in vivo analysis of embryogenesis and organogenesis. These characteristics can also be exploited by researchers interested in signaling pathways and disease processes and, accordingly, there is a growing literature on the use of zebrafish to model human disease. This model holds great potential for exploring how autophagy, an evolutionarily conserved mechanism for protein degradation, influences the pathogeneses of a range of different human diseases and for the evaluation of this pathway as a potential therapeutic strategy. Here we summarize what is known about the regulation of autophagy in eukaryotic cells and its role in neurodegenerative disease and highlight how research using zebrafish has helped further our understanding of these processes. Elsevier Pub. Co 2011-04 /pmc/articles/PMC3060341/ /pubmed/21256213 http://dx.doi.org/10.1016/j.bbadis.2011.01.004 Text en © 2011 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Review
Fleming, Angeleen
Rubinsztein, David C.
Zebrafish as a model to understand autophagy and its role in neurological disease()
title Zebrafish as a model to understand autophagy and its role in neurological disease()
title_full Zebrafish as a model to understand autophagy and its role in neurological disease()
title_fullStr Zebrafish as a model to understand autophagy and its role in neurological disease()
title_full_unstemmed Zebrafish as a model to understand autophagy and its role in neurological disease()
title_short Zebrafish as a model to understand autophagy and its role in neurological disease()
title_sort zebrafish as a model to understand autophagy and its role in neurological disease()
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060341/
https://www.ncbi.nlm.nih.gov/pubmed/21256213
http://dx.doi.org/10.1016/j.bbadis.2011.01.004
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