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The Secrets of Alternative Autophagy

For many years, it was thought that ATG5 and ATG7 played a pivotal role in autophagy, and that the knockdown of one of these genes would result in its inhibition. However, cells with ATG5 or ATG7 depletion still generate autophagic vacuoles with mainly trans-Golgi-originated isolation membranes and...

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Autores principales: Urbańska, Kaja, Orzechowski, Arkadiusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623506/
https://www.ncbi.nlm.nih.gov/pubmed/34831462
http://dx.doi.org/10.3390/cells10113241
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author Urbańska, Kaja
Orzechowski, Arkadiusz
author_facet Urbańska, Kaja
Orzechowski, Arkadiusz
author_sort Urbańska, Kaja
collection PubMed
description For many years, it was thought that ATG5 and ATG7 played a pivotal role in autophagy, and that the knockdown of one of these genes would result in its inhibition. However, cells with ATG5 or ATG7 depletion still generate autophagic vacuoles with mainly trans-Golgi-originated isolation membranes and do not die. This indicates that autophagy can occur via ATG5/ATG7-independent alternative autophagy. Its molecular mechanism differs from that of the canonical pathway, including inter alia the phosphorylation of ULK1, and lack of LC3 modifications. As the alternative autophagy pathway has only recently been described, little is known of its precise role; however, a considerable body of evidence suggests that alternative autophagy participates in mitochondrion removal. This review summarizes the latest progress made in research on alternative autophagy and describes its possible molecular mechanism, roles and methods of detection, and possible modulators. There is a need for further research focused on types of autophagy, as this can elucidate the functioning of various cell types and the pathogenesis of human and animal diseases.
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spelling pubmed-86235062021-11-27 The Secrets of Alternative Autophagy Urbańska, Kaja Orzechowski, Arkadiusz Cells Review For many years, it was thought that ATG5 and ATG7 played a pivotal role in autophagy, and that the knockdown of one of these genes would result in its inhibition. However, cells with ATG5 or ATG7 depletion still generate autophagic vacuoles with mainly trans-Golgi-originated isolation membranes and do not die. This indicates that autophagy can occur via ATG5/ATG7-independent alternative autophagy. Its molecular mechanism differs from that of the canonical pathway, including inter alia the phosphorylation of ULK1, and lack of LC3 modifications. As the alternative autophagy pathway has only recently been described, little is known of its precise role; however, a considerable body of evidence suggests that alternative autophagy participates in mitochondrion removal. This review summarizes the latest progress made in research on alternative autophagy and describes its possible molecular mechanism, roles and methods of detection, and possible modulators. There is a need for further research focused on types of autophagy, as this can elucidate the functioning of various cell types and the pathogenesis of human and animal diseases. MDPI 2021-11-19 /pmc/articles/PMC8623506/ /pubmed/34831462 http://dx.doi.org/10.3390/cells10113241 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Urbańska, Kaja
Orzechowski, Arkadiusz
The Secrets of Alternative Autophagy
title The Secrets of Alternative Autophagy
title_full The Secrets of Alternative Autophagy
title_fullStr The Secrets of Alternative Autophagy
title_full_unstemmed The Secrets of Alternative Autophagy
title_short The Secrets of Alternative Autophagy
title_sort secrets of alternative autophagy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623506/
https://www.ncbi.nlm.nih.gov/pubmed/34831462
http://dx.doi.org/10.3390/cells10113241
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