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Autophagy

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DOI
10.7892/boris.95351
Publisher DOI
10.1002/9780470015902.a0021581.pub2
Abstract
Autophagy comprises several evolutionarily conserved mechanisms for transport and uptake of proteins and even cytoplasmic organelles into the lysosome. Macroautophagy sequesters cytoplasmic elements, sometimes with elegant selectivity and sometimes just in bulk, into double membrane vacuoles which are subsequently fused with lysosomes for degradation. In mammals, such recycling of protein aggregates and malfunctioning organelles allows macroautophagy to facilitate recovery of constituents for new protein synthesis or ATP (adenosine triphosphate) production, but provides also for selective removal of signalling proteins (e.g. signalphagy) and serves as an effective mechanism for quality control on whole organelles (e.g. mitophagy). Autophagy signalling includes both numerous options for its regulation by posttranslational modifications, for example phosphorylation/dephosphorylation and acetylation/deacetylation, as well as by transcriptional upregulation with many transcription factors. Autophagy shares functional components with other pathways and stands always balanced between different cell fates: quiescence, that is a temporary cell cycle arrest, senescence or cell death by apoptotic or nonapoptotic mechanisms.
Date Issued
2017
Publication Type
Subject(s)
600 Technology > 610 Medicine & health
Language(s)
de
Author(s)
Simon, Hans-Uwe
Institut für Pharmakologie
Friis, Robert
Institut für Pharmakologie
Colombo, María I.
Additional Credits
Institut für Pharmakologie
Publisher
Wiley
Book Title
eLS Citable reviews in the life sciences
Access(Rights)
restricted
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