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Pexophagy: A Model for Selective Autophagy

The removal of damaged or superfluous organelles from the cytosol by selective autophagy is required to maintain organelle function, quality control and overall cellular homeostasis. Precisely how substrate selectivity is achieved, and how individual substrates are degraded during selective autophag...

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Detalles Bibliográficos
Autores principales: Germain, Kyla, Kim, Peter K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013971/
https://www.ncbi.nlm.nih.gov/pubmed/31963200
http://dx.doi.org/10.3390/ijms21020578
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author Germain, Kyla
Kim, Peter K.
author_facet Germain, Kyla
Kim, Peter K.
author_sort Germain, Kyla
collection PubMed
description The removal of damaged or superfluous organelles from the cytosol by selective autophagy is required to maintain organelle function, quality control and overall cellular homeostasis. Precisely how substrate selectivity is achieved, and how individual substrates are degraded during selective autophagy in response to both extracellular and intracellular cues is not well understood. The aim of this review is to highlight pexophagy, the autophagic degradation of peroxisomes, as a model for selective autophagy. Peroxisomes are dynamic organelles whose abundance is rapidly modulated in response to metabolic demands. Peroxisomes are routinely turned over by pexophagy for organelle quality control yet can also be degraded by pexophagy in response to external stimuli such as amino acid starvation or hypoxia. This review discusses the molecular machinery and regulatory mechanisms governing substrate selectivity during both quality-control pexophagy and pexophagy in response to external stimuli, in yeast and mammalian systems. We draw lessons from pexophagy to infer how the cell may coordinate the degradation of individual substrates by selective autophagy across different cellular cues.
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spelling pubmed-70139712020-03-09 Pexophagy: A Model for Selective Autophagy Germain, Kyla Kim, Peter K. Int J Mol Sci Review The removal of damaged or superfluous organelles from the cytosol by selective autophagy is required to maintain organelle function, quality control and overall cellular homeostasis. Precisely how substrate selectivity is achieved, and how individual substrates are degraded during selective autophagy in response to both extracellular and intracellular cues is not well understood. The aim of this review is to highlight pexophagy, the autophagic degradation of peroxisomes, as a model for selective autophagy. Peroxisomes are dynamic organelles whose abundance is rapidly modulated in response to metabolic demands. Peroxisomes are routinely turned over by pexophagy for organelle quality control yet can also be degraded by pexophagy in response to external stimuli such as amino acid starvation or hypoxia. This review discusses the molecular machinery and regulatory mechanisms governing substrate selectivity during both quality-control pexophagy and pexophagy in response to external stimuli, in yeast and mammalian systems. We draw lessons from pexophagy to infer how the cell may coordinate the degradation of individual substrates by selective autophagy across different cellular cues. MDPI 2020-01-16 /pmc/articles/PMC7013971/ /pubmed/31963200 http://dx.doi.org/10.3390/ijms21020578 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Germain, Kyla
Kim, Peter K.
Pexophagy: A Model for Selective Autophagy
title Pexophagy: A Model for Selective Autophagy
title_full Pexophagy: A Model for Selective Autophagy
title_fullStr Pexophagy: A Model for Selective Autophagy
title_full_unstemmed Pexophagy: A Model for Selective Autophagy
title_short Pexophagy: A Model for Selective Autophagy
title_sort pexophagy: a model for selective autophagy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7013971/
https://www.ncbi.nlm.nih.gov/pubmed/31963200
http://dx.doi.org/10.3390/ijms21020578
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