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Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration
Cell identity involves both selective gene activity and specialization of cytoplasmic architecture and protein machinery. Similarly, reprogramming differentiated cells requires both genetic program alterations and remodeling of the cellular architecture. While changes in genetic and epigenetic progr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066936/ https://www.ncbi.nlm.nih.gov/pubmed/27467399 http://dx.doi.org/10.1080/15548627.2016.1207015 |
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author | Saera-Vila, Alfonso Kish, Phillip E. Louie, Ke'ale W. Grzegorski, Steven J. Klionsky, Daniel J. Kahana, Alon |
author_facet | Saera-Vila, Alfonso Kish, Phillip E. Louie, Ke'ale W. Grzegorski, Steven J. Klionsky, Daniel J. Kahana, Alon |
author_sort | Saera-Vila, Alfonso |
collection | PubMed |
description | Cell identity involves both selective gene activity and specialization of cytoplasmic architecture and protein machinery. Similarly, reprogramming differentiated cells requires both genetic program alterations and remodeling of the cellular architecture. While changes in genetic and epigenetic programs have been well documented in dedifferentiating cells, the pathways responsible for remodeling the cellular architecture and eliminating specialized protein complexes are not as well understood. Here, we utilize a zebrafish model of adult muscle regeneration to study cytoplasmic remodeling during cell dedifferentiation. We describe activation of autophagy early in the regenerative response to muscle injury, while blocking autophagy using chloroquine or Atg5 and Becn1 knockdown reduced the rate of regeneration with accumulation of sarcomeric and nuclear debris. We further identify Casp3/caspase 3 as a candidate mediator of cellular reprogramming and Fgf signaling as an important activator of autophagy in dedifferentiating myocytes. We conclude that autophagy plays a critical role in cell reprogramming by regulating cytoplasmic remodeling, facilitating the transition to a less differentiated cell identity. |
format | Online Article Text |
id | pubmed-5066936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-50669362016-10-21 Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration Saera-Vila, Alfonso Kish, Phillip E. Louie, Ke'ale W. Grzegorski, Steven J. Klionsky, Daniel J. Kahana, Alon Autophagy Basic Research Papers Cell identity involves both selective gene activity and specialization of cytoplasmic architecture and protein machinery. Similarly, reprogramming differentiated cells requires both genetic program alterations and remodeling of the cellular architecture. While changes in genetic and epigenetic programs have been well documented in dedifferentiating cells, the pathways responsible for remodeling the cellular architecture and eliminating specialized protein complexes are not as well understood. Here, we utilize a zebrafish model of adult muscle regeneration to study cytoplasmic remodeling during cell dedifferentiation. We describe activation of autophagy early in the regenerative response to muscle injury, while blocking autophagy using chloroquine or Atg5 and Becn1 knockdown reduced the rate of regeneration with accumulation of sarcomeric and nuclear debris. We further identify Casp3/caspase 3 as a candidate mediator of cellular reprogramming and Fgf signaling as an important activator of autophagy in dedifferentiating myocytes. We conclude that autophagy plays a critical role in cell reprogramming by regulating cytoplasmic remodeling, facilitating the transition to a less differentiated cell identity. Taylor & Francis 2016-07-28 /pmc/articles/PMC5066936/ /pubmed/27467399 http://dx.doi.org/10.1080/15548627.2016.1207015 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC 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. The moral rights of the named author(s) have been asserted. |
spellingShingle | Basic Research Papers Saera-Vila, Alfonso Kish, Phillip E. Louie, Ke'ale W. Grzegorski, Steven J. Klionsky, Daniel J. Kahana, Alon Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration |
title | Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration |
title_full | Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration |
title_fullStr | Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration |
title_full_unstemmed | Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration |
title_short | Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration |
title_sort | autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration |
topic | Basic Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066936/ https://www.ncbi.nlm.nih.gov/pubmed/27467399 http://dx.doi.org/10.1080/15548627.2016.1207015 |
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