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Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy

Protein aggregation is a continuous process in our cells. Some proteins aggregate in a regulated manner required for different vital functional processes in the cells whereas other protein aggregates result from misfolding caused by various stressors. The decision to form an aggregate is largely mad...

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Detalles Bibliográficos
Autores principales: Lamark, Trond, Johansen, Terje
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320095/
https://www.ncbi.nlm.nih.gov/pubmed/22518139
http://dx.doi.org/10.1155/2012/736905
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author Lamark, Trond
Johansen, Terje
author_facet Lamark, Trond
Johansen, Terje
author_sort Lamark, Trond
collection PubMed
description Protein aggregation is a continuous process in our cells. Some proteins aggregate in a regulated manner required for different vital functional processes in the cells whereas other protein aggregates result from misfolding caused by various stressors. The decision to form an aggregate is largely made by chaperones and chaperone-assisted proteins. Proteins that are damaged beyond repair are degraded either by the proteasome or by the lysosome via autophagy. The aggregates can be degraded by the proteasome and by chaperone-mediated autophagy only after dissolution into soluble single peptide species. Hence, protein aggregates as such are degraded by macroautophagy. The selective degradation of protein aggregates by macroautophagy is called aggrephagy. Here we review the processes of aggregate formation, recognition, transport, and sequestration into autophagosomes by autophagy receptors and the role of aggrephagy in different protein aggregation diseases.
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spelling pubmed-33200952012-04-19 Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy Lamark, Trond Johansen, Terje Int J Cell Biol Review Article Protein aggregation is a continuous process in our cells. Some proteins aggregate in a regulated manner required for different vital functional processes in the cells whereas other protein aggregates result from misfolding caused by various stressors. The decision to form an aggregate is largely made by chaperones and chaperone-assisted proteins. Proteins that are damaged beyond repair are degraded either by the proteasome or by the lysosome via autophagy. The aggregates can be degraded by the proteasome and by chaperone-mediated autophagy only after dissolution into soluble single peptide species. Hence, protein aggregates as such are degraded by macroautophagy. The selective degradation of protein aggregates by macroautophagy is called aggrephagy. Here we review the processes of aggregate formation, recognition, transport, and sequestration into autophagosomes by autophagy receptors and the role of aggrephagy in different protein aggregation diseases. Hindawi Publishing Corporation 2012 2012-03-22 /pmc/articles/PMC3320095/ /pubmed/22518139 http://dx.doi.org/10.1155/2012/736905 Text en Copyright © 2012 T. Lamark and T. Johansen. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Lamark, Trond
Johansen, Terje
Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy
title Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy
title_full Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy
title_fullStr Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy
title_full_unstemmed Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy
title_short Aggrephagy: Selective Disposal of Protein Aggregates by Macroautophagy
title_sort aggrephagy: selective disposal of protein aggregates by macroautophagy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320095/
https://www.ncbi.nlm.nih.gov/pubmed/22518139
http://dx.doi.org/10.1155/2012/736905
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