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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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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

WIPI-1alpha (WIPI49), a member of the novel 7-bladed WIPI protein family, is aberrantly expressed in human cancer and is linked to starvation-induced autophagy

TL;DR: The data suggest that WIPI proteins share an evolutionary conserved function in autophagy and that autophagic capacity may be compromised in human cancers.
Journal ArticleDOI

Autophagic Components Contribute to Hypersensitive Cell Death in Arabidopsis

TL;DR: Autophagic cell death contributes to HR PCD and can function in parallel with other prodeath pathways, and it is demonstrated that PCD triggered by coiled-coil (CC)-type immune receptors via NDR1 is either autophagy-independent or engages autophagic components with cathepsins and other unidentified cell death mediators.
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Chemical modulators of autophagy as biological probes and potential therapeutics.

TL;DR: The roles of mammalian autophagy in health and disease are discussed and recent advances in pharmacological manipulation of autophagic pathways are highlighted as a therapeutic strategy for a variety of pathological conditions.
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A multispecificity syntaxin homologue, Vam3p, essential for autophagic and biosynthetic protein transport to the vacuole.

TL;DR: Vam3p appears to function as a multispecificity receptor in heterotypic membrane docking and fusion reactions with the vacuole, indicating that SNAREs alone do not define the specificity of vesicle docking reactions.
Journal ArticleDOI

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

TL;DR: Mutation screening of positional candidate genes in the PDB3 locus in patients with PDB confirmed that mutations affecting the ubiquitin-binding domain of SQSTM1 are a common cause of familial and sporadic Paget's disease of bone.
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

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Trending Questions (2)
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.

Is 20 hours enough for autophagy?

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