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siRNA screening reveals that SNAP29 contributes to exosome release

Cells release extracellular vesicles (EVs) of different sizes. Small EVs (< 200 nm) can originate from the fusion of multivesicular bodies with the plasma membrane, i.e. exosomes, and from budding of the plasma membrane, i.e. small ectosomes. To investigate the molecular machinery required for th...

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Autores principales: Hessvik, Nina Pettersen, Sagini, Krizia, Romero, Silvana, Ramirez-Garrastacho, Manuel, Rodriguez, Marta, Tutturen, Astrid Elisabeth V., Kvalvaag, Audun, Stang, Espen, Brech, Andreas, Sandvig, Kirsten, Llorente, Alicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247572/
https://www.ncbi.nlm.nih.gov/pubmed/37285022
http://dx.doi.org/10.1007/s00018-023-04822-8
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author Hessvik, Nina Pettersen
Sagini, Krizia
Romero, Silvana
Ramirez-Garrastacho, Manuel
Rodriguez, Marta
Tutturen, Astrid Elisabeth V.
Kvalvaag, Audun
Stang, Espen
Brech, Andreas
Sandvig, Kirsten
Llorente, Alicia
author_facet Hessvik, Nina Pettersen
Sagini, Krizia
Romero, Silvana
Ramirez-Garrastacho, Manuel
Rodriguez, Marta
Tutturen, Astrid Elisabeth V.
Kvalvaag, Audun
Stang, Espen
Brech, Andreas
Sandvig, Kirsten
Llorente, Alicia
author_sort Hessvik, Nina Pettersen
collection PubMed
description Cells release extracellular vesicles (EVs) of different sizes. Small EVs (< 200 nm) can originate from the fusion of multivesicular bodies with the plasma membrane, i.e. exosomes, and from budding of the plasma membrane, i.e. small ectosomes. To investigate the molecular machinery required for the release of small EVs, we developed a sensitive assay based on incorporation of radioactive cholesterol in EV membranes and used it in a siRNA screening. The screening showed that depletion of several SNARE proteins affected the release of small EVs. We focused on SNAP29, VAMP8, syntaxin 2, syntaxin 3 and syntaxin 18, the depletion of which reduced the release of small EVs. Importantly, this result was verified using gold standard techniques. SNAP29 depletion resulted in the largest effect and was further investigated. Immunoblotting analysis of small EVs showed that the release of several proteins considered to be associated with exosomes like syntenin, CD63 and Tsg101 was reduced, while the level of several proteins that have been shown to be released in ectosomes (annexins) or by secretory autophagy (LC3B and p62) was not affected by SNAP29 depletion. Moreover, these proteins appeared in different fractions when the EV samples were further separated by a density gradient. These results suggest that SNAP29 depletion mainly affects the secretion of exosomes. To investigate how SNAP29 affects exosome release, we used microscopy to study the distribution of MBVs using CD63 labelling and CD63-pHluorin to detect fusion events of MVBs with the plasma membrane. SNAP29 depletion caused a redistribution of CD63-labelled compartments but did not change the number of fusion events. Further experiments are therefore needed to fully understand the function of SNAP29. To conclude, we have developed a novel screening assay that has allowed us to identify several SNAREs involved in the release of small EVs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-023-04822-8.
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spelling pubmed-102475722023-06-09 siRNA screening reveals that SNAP29 contributes to exosome release Hessvik, Nina Pettersen Sagini, Krizia Romero, Silvana Ramirez-Garrastacho, Manuel Rodriguez, Marta Tutturen, Astrid Elisabeth V. Kvalvaag, Audun Stang, Espen Brech, Andreas Sandvig, Kirsten Llorente, Alicia Cell Mol Life Sci Original Article Cells release extracellular vesicles (EVs) of different sizes. Small EVs (< 200 nm) can originate from the fusion of multivesicular bodies with the plasma membrane, i.e. exosomes, and from budding of the plasma membrane, i.e. small ectosomes. To investigate the molecular machinery required for the release of small EVs, we developed a sensitive assay based on incorporation of radioactive cholesterol in EV membranes and used it in a siRNA screening. The screening showed that depletion of several SNARE proteins affected the release of small EVs. We focused on SNAP29, VAMP8, syntaxin 2, syntaxin 3 and syntaxin 18, the depletion of which reduced the release of small EVs. Importantly, this result was verified using gold standard techniques. SNAP29 depletion resulted in the largest effect and was further investigated. Immunoblotting analysis of small EVs showed that the release of several proteins considered to be associated with exosomes like syntenin, CD63 and Tsg101 was reduced, while the level of several proteins that have been shown to be released in ectosomes (annexins) or by secretory autophagy (LC3B and p62) was not affected by SNAP29 depletion. Moreover, these proteins appeared in different fractions when the EV samples were further separated by a density gradient. These results suggest that SNAP29 depletion mainly affects the secretion of exosomes. To investigate how SNAP29 affects exosome release, we used microscopy to study the distribution of MBVs using CD63 labelling and CD63-pHluorin to detect fusion events of MVBs with the plasma membrane. SNAP29 depletion caused a redistribution of CD63-labelled compartments but did not change the number of fusion events. Further experiments are therefore needed to fully understand the function of SNAP29. To conclude, we have developed a novel screening assay that has allowed us to identify several SNAREs involved in the release of small EVs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00018-023-04822-8. Springer International Publishing 2023-06-07 2023 /pmc/articles/PMC10247572/ /pubmed/37285022 http://dx.doi.org/10.1007/s00018-023-04822-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Hessvik, Nina Pettersen
Sagini, Krizia
Romero, Silvana
Ramirez-Garrastacho, Manuel
Rodriguez, Marta
Tutturen, Astrid Elisabeth V.
Kvalvaag, Audun
Stang, Espen
Brech, Andreas
Sandvig, Kirsten
Llorente, Alicia
siRNA screening reveals that SNAP29 contributes to exosome release
title siRNA screening reveals that SNAP29 contributes to exosome release
title_full siRNA screening reveals that SNAP29 contributes to exosome release
title_fullStr siRNA screening reveals that SNAP29 contributes to exosome release
title_full_unstemmed siRNA screening reveals that SNAP29 contributes to exosome release
title_short siRNA screening reveals that SNAP29 contributes to exosome release
title_sort sirna screening reveals that snap29 contributes to exosome release
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247572/
https://www.ncbi.nlm.nih.gov/pubmed/37285022
http://dx.doi.org/10.1007/s00018-023-04822-8
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