Localized


Journal

Autophagy
ISSN: 1554-8635
Titre abrégé: Autophagy
Pays: United States
ID NLM: 101265188

Informations de publication

Date de publication:
04 2020
Historique:
pubmed: 6 2 2020
medline: 8 6 2021
entrez: 5 2 2020
Statut: ppublish

Résumé

During (macro)autophagy, cells form transient organelles, termed autophagosomes, to target a broad spectrum of substrates for degradation critical to cellular and organismal health. Driven by rapid membrane assembly, an initially small vesicle (phagophore) elongates into a large cup-shaped structure to engulf substrates within a few minutes in a double-membrane autophagosome. In particular, how autophagic membranes expand has been a longstanding question. Here, we summarize our recent work that delineates a pathway that drives phagophore expansion by localized

Identifiants

pubmed: 32013690
doi: 10.1080/15548627.2020.1725379
pmc: PMC7138244
doi:

Substances chimiques

Autophagy-Related Proteins 0
Fatty Acids 0
Phospholipids 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

770-771

Références

Cell. 2020 Jan 9;180(1):135-149.e14
pubmed: 31883797

Auteurs

Maximilian Schütter (M)

Group of Autophagy and Cellular Ageing, Max Planck Institute for Biology of Ageing, Cologne, Germany.

Martin Graef (M)

Group of Autophagy and Cellular Ageing, Max Planck Institute for Biology of Ageing, Cologne, Germany.
Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.

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Classifications MeSH