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The variability of autophagy and cell death susceptibility: Unanswered questions

Impaired autophagic machinery is implicated in a number of diseases such as heart disease, neurodegeneration and cancer. A common denominator in these pathologies is a dysregulation of autophagy that has been linked to a change in susceptibility to cell death. Although we have progressed in understa...

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Autores principales: Loos, Ben, Engelbrecht, Anna-Mart, Lockshin, Richard A., Klionsky, Daniel J, Zakeri, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026026/
https://www.ncbi.nlm.nih.gov/pubmed/23846383
http://dx.doi.org/10.4161/auto.25560
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author Loos, Ben
Engelbrecht, Anna-Mart
Lockshin, Richard A.
Klionsky, Daniel J
Zakeri, Zahra
author_facet Loos, Ben
Engelbrecht, Anna-Mart
Lockshin, Richard A.
Klionsky, Daniel J
Zakeri, Zahra
author_sort Loos, Ben
collection PubMed
description Impaired autophagic machinery is implicated in a number of diseases such as heart disease, neurodegeneration and cancer. A common denominator in these pathologies is a dysregulation of autophagy that has been linked to a change in susceptibility to cell death. Although we have progressed in understanding the molecular machinery and regulation of the autophagic pathway, many unanswered questions remain. How does the metabolic contribution of autophagy connect with the cell’s history and how does its current autophagic flux affect metabolic status and susceptibility to undergo cell death? How does autophagic flux operate to switch metabolic direction and what are the underlying mechanisms in metabolite and energetic sensing, metabolite substrate provision and metabolic integration during the cellular stress response? In this article we focus on unresolved questions that address issues around the role of autophagy in sensing the energetic environment and its role in actively generating metabolite substrates. We attempt to provide answers by explaining how and when a change in autophagic pathway activity such as primary stress response is able to affect cell viability and when not. By addressing the dynamic metabolic relationship between autophagy, apoptosis and necrosis we provide a new perspective on the parameters that connect autophagic activity, severity of injury and cellular history in a logical manner. Last, by evaluating the cell’s condition and autophagic activity in a clear context of regulatory parameters in the intra- and extracellular environment, this review provides new concepts that set autophagy into an energetic feedback loop, that may assist in our understanding of autophagy in maintaining healthy cells or when it controls the threshold between cell death and cell survival.
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spelling pubmed-40260262014-05-20 The variability of autophagy and cell death susceptibility: Unanswered questions Loos, Ben Engelbrecht, Anna-Mart Lockshin, Richard A. Klionsky, Daniel J Zakeri, Zahra Autophagy Review Impaired autophagic machinery is implicated in a number of diseases such as heart disease, neurodegeneration and cancer. A common denominator in these pathologies is a dysregulation of autophagy that has been linked to a change in susceptibility to cell death. Although we have progressed in understanding the molecular machinery and regulation of the autophagic pathway, many unanswered questions remain. How does the metabolic contribution of autophagy connect with the cell’s history and how does its current autophagic flux affect metabolic status and susceptibility to undergo cell death? How does autophagic flux operate to switch metabolic direction and what are the underlying mechanisms in metabolite and energetic sensing, metabolite substrate provision and metabolic integration during the cellular stress response? In this article we focus on unresolved questions that address issues around the role of autophagy in sensing the energetic environment and its role in actively generating metabolite substrates. We attempt to provide answers by explaining how and when a change in autophagic pathway activity such as primary stress response is able to affect cell viability and when not. By addressing the dynamic metabolic relationship between autophagy, apoptosis and necrosis we provide a new perspective on the parameters that connect autophagic activity, severity of injury and cellular history in a logical manner. Last, by evaluating the cell’s condition and autophagic activity in a clear context of regulatory parameters in the intra- and extracellular environment, this review provides new concepts that set autophagy into an energetic feedback loop, that may assist in our understanding of autophagy in maintaining healthy cells or when it controls the threshold between cell death and cell survival. Landes Bioscience 2013-09-01 2013-07-10 /pmc/articles/PMC4026026/ /pubmed/23846383 http://dx.doi.org/10.4161/auto.25560 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Loos, Ben
Engelbrecht, Anna-Mart
Lockshin, Richard A.
Klionsky, Daniel J
Zakeri, Zahra
The variability of autophagy and cell death susceptibility: Unanswered questions
title The variability of autophagy and cell death susceptibility: Unanswered questions
title_full The variability of autophagy and cell death susceptibility: Unanswered questions
title_fullStr The variability of autophagy and cell death susceptibility: Unanswered questions
title_full_unstemmed The variability of autophagy and cell death susceptibility: Unanswered questions
title_short The variability of autophagy and cell death susceptibility: Unanswered questions
title_sort variability of autophagy and cell death susceptibility: unanswered questions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026026/
https://www.ncbi.nlm.nih.gov/pubmed/23846383
http://dx.doi.org/10.4161/auto.25560
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