ATG9A vesicles are a subtype of intracellular nanovesicle

Cells are filled with thousands of vesicles, which mediate protein transport and ensure homeostasis of the endomembrane system. Distinguishing these vesicles functionally and molecularly represents a major challenge. Intracellular nanovesicles (INVs) are a large class of transport vesicles that likely comprise multiple subtypes. Here, we define the INV proteome and find that it is molecularly heterogeneous and enriched for transmembrane cargo molecules, including integrins, transporters and ATG9A, a lipid scramblase associated with autophagy. ATG9A is known to reside in 'ATG9A vesicles' - small vesicles that contribute to autophagosome formation. Here, using in-cell vesicle capture assays, we found that ATG9A, as well as other ATG9A vesicle cargoes, are in INVs. Quantitative analysis showed that virtually all ATG9A vesicles are INVs, but that only ∼20% of INVs are ATG9A vesicles, suggesting that ATG9A vesicles are in fact a subtype of INV, which we term ATG9A-flavor INVs. Finally, we show that perturbing ATG9A-flavor INVs impairs the autophagy response induced by starvation.

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Publication Details

Journal
Journal of Cell Science
Published
2025-03-11
DOI
https://doi.org/10.1242/jcs.263852
Citations
6
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
4.84

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article

ATG9A vesicles are a subtype of intracellular nanovesicle

Daniel J. Moore, Stephen Royle, Mary Fesenko, Peyton Ewbank et al.
6 citations
Journal of Cell Science
Extracellular vesicles in disease
4.84
article

ATG9A vesicles are a subtype of intracellular nanovesicle

Daniel J. Moore, Stephen Royle, Mary Fesenko, Peyton Ewbank, Elizabeth Courthold
article en
6 citations

Abstract

Cells are filled with thousands of vesicles, which mediate protein transport and ensure homeostasis of the endomembrane system. Distinguishing these vesicles functionally and molecularly represents a major challenge. Intracellular nanovesicles (INVs) are a large class of transport vesicles that likely comprise multiple subtypes. Here, we define the INV proteome and find that it is molecularly heterogeneous and enriched for transmembrane cargo molecules, including integrins, transporters and ATG9A, a lipid scramblase associated with autophagy. ATG9A is known to reside in 'ATG9A vesicles' - small vesicles that contribute to autophagosome formation. Here, using in-cell vesicle capture assays, we found that ATG9A, as well as other ATG9A vesicle cargoes, are in INVs. Quantitative analysis showed that virtually all ATG9A vesicles are INVs, but that only ∼20% of INVs are ATG9A vesicles, suggesting that ATG9A vesicles are in fact a subtype of INV, which we term ATG9A-flavor INVs. Finally, we show that perturbing ATG9A-flavor INVs impairs the autophagy response induced by starvation.

Journal of Cell ScienceVol. 138(7)
University of Warwick (GB)
Biotechnology and Biological Sciences Research Council
Life below water
Openalex Percentile: Top 5%
Extracellular vesicles in disease
4.84
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