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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, +2983 more
- 08 Feb 2021 - 
- Vol. 17, Iss: 1, pp 1-382
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TLDR
In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
Abstract
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.

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Citations
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Journal ArticleDOI

Autophagy in major human diseases

Daniel J. Klionsky, +71 more
- 01 Oct 2021 - 
TL;DR: In this paper, preclinical data linking autophagy dysfunction to the pathogenesis of major human disorders including cancer as well as cardiovascular, neurodegenerative, metabolic, pulmonary, renal, infectious, musculoskeletal, and ocular disorders.
Journal ArticleDOI

Autophagy in metabolic disease and ageing.

TL;DR: The role of autophagy in the pathogenesis of metabolic diseases associated with or occurring in the context of ageing, including insulin resistance, T2DM and sarcopenic obesity, was discussed in this article.
Journal ArticleDOI

The SARS-CoV-2 protein ORF3a inhibits fusion of autophagosomes with lysosomes

TL;DR: In this article, the authors systematically screened 28 viral proteins of SARS-CoV-2 and identified that ORF3a strongly inhibited autophagic flux by blocking the fusion of autophagosomes with lysosomes.
Journal ArticleDOI

The STING1 network regulates autophagy and cell death.

TL;DR: The latest advances in the understanding of the regulating mechanisms and signaling pathways of STING1 in autophagy and cell death are outlined, which may shed light on new targets for therapeutic interventions.
References
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Journal ArticleDOI

Atg101, a novel mammalian autophagy protein interacting with Atg13

TL;DR: Data suggest that Atg101 is a novel Atg protein that functions together with ULK, Atg13 and FIP200, and is important for the stability and basal phosphorylation of AtG13 and ULK1.
Journal ArticleDOI

p62 Is a Key Regulator of Nutrient Sensing in the mTORC1 Pathway

TL;DR: The signaling adaptor p62 is an integral part of the mTORC1 complex and is necessary to mediate amino acid signaling for the activation of S6K1 and 4EBP1 and is identified as an interacting partner of raptor.
Journal ArticleDOI

NF-κB Activation Represses Tumor Necrosis Factor-α-induced Autophagy

TL;DR: It is shown that NF-κB activation mediates repression of autophagy in tumor necrosis factor-α-treated Ewing sarcoma cells, and it is suggested that stimulation of Autophagy may be a potential way bypassing the resistance of cancer cells to anti-cancer agents that activate NF-σκB.
Journal ArticleDOI

Global regulation of erythroid gene expression by transcription factor GATA-1

TL;DR: It is demonstrated that selected regions of the Fog1 gene exhibit enhancer activity and in vivo occupancy by GATA-1, which defines a regulatory loop for beta globin expression and demonstrates how transcriptome analysis can be used to generate testable hypotheses regarding transcriptional networks.
Journal ArticleDOI

siRNA screening of the kinome identifies ULK1 as a multidomain modulator of autophagy

TL;DR: Experiments reveal at least two domains in ULK1 which likely function via unique sets of effectors to regulate autophagy, consistent with a role downstream of mTOR.
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

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Trending Questions (2)
How long does it take for body to reach autophagy?

Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms.

What does autophagy do Reddit?

Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway.