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• W2604133228 abstract "Macroautophagy/autophagy plays a role in unconventional secretion of leaderless cytosolic proteins. Whether and how secretory autophagy diverges from conventional degradative autophagy is unclear. We have shown that the prototypical secretory autophagy cargo IL1B/IL-1β (interleukin 1 β) is recognized by TRIM16, and that this first to be identified secretory autophagy receptor interacts with the R-SNARE SEC22B to jointly deliver cargo to the MAP1LC3B-II-positive sequestration membranes. Cargo secretion is unaffected by knockdowns of STX17, a SNARE catalyzing autophagosome-lysosome fusion as a prelude to cargo degradation. Instead, SEC22B in combination with plasma membrane syntaxins completes cargo secretion. Thus, secretory autophagy diverges from degradative autophagy by using specialized receptors and a dedicated SNARE machinery to bypass fusion with lysosomes." @default.
• W2604133228 created "2017-04-14" @default.
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• W2604133228 date "2017-04-17" @default.
• W2604133228 modified "2023-10-13" @default.
• W2604133228 title "Cellular and molecular mechanism for secretory autophagy" @default.
• W2604133228 doi "https://doi.org/10.1080/15548627.2017.1307486" @default.
• W2604133228 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5486376" @default.
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