Cargando…
Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair
Exosomes are an extracellular vesicle (EV) subtype that is secreted upon the fusion of multivesicular bodies (MVBs) with the plasma membrane. Exosomes may participate in intercellular communication and have utility as disease biomarkers; however, little is known regarding the physiological stimuli t...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241516/ https://www.ncbi.nlm.nih.gov/pubmed/37204294 http://dx.doi.org/10.7554/eLife.86556 |
_version_ | 1785054001283203072 |
---|---|
author | Williams, Justin Krish Ngo, Jordan Matthew Lehman, Isabelle Madeline Schekman, Randy |
author_facet | Williams, Justin Krish Ngo, Jordan Matthew Lehman, Isabelle Madeline Schekman, Randy |
author_sort | Williams, Justin Krish |
collection | PubMed |
description | Exosomes are an extracellular vesicle (EV) subtype that is secreted upon the fusion of multivesicular bodies (MVBs) with the plasma membrane. Exosomes may participate in intercellular communication and have utility as disease biomarkers; however, little is known regarding the physiological stimuli that induce their secretion. Ca(2+) influx promotes exosome secretion, raising the possibility that exosomes are secreted during the Ca(2+)-dependent plasma membrane repair of tissues damaged by mechanical stress in vivo. To determine whether exosomes are secreted upon plasma membrane damage, we developed sensitive assays to measure exosome secretion in intact and permeabilized cells. Our results suggest that exosome secretion is coupled to Ca(2+)-dependent plasma membrane repair. We find that annexin A6 (ANXA6), a well-known plasma membrane repair protein, is recruited to MVBs in the presence of Ca(2+) and required for Ca(2+)-dependent exosome secretion, both in intact and in permeabilized cells. ANXA6 depletion stalls MVBs at the cell periphery, and ANXA6 truncations localize to different membranes, suggesting that ANXA6 may serve to tether MVBs to the plasma membrane. We find that cells secrete exosomes and other EVs upon plasma membrane damage and propose that repair-induced secretion may contribute to the pool of EVs present within biological fluids. |
format | Online Article Text |
id | pubmed-10241516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-102415162023-06-06 Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair Williams, Justin Krish Ngo, Jordan Matthew Lehman, Isabelle Madeline Schekman, Randy eLife Cell Biology Exosomes are an extracellular vesicle (EV) subtype that is secreted upon the fusion of multivesicular bodies (MVBs) with the plasma membrane. Exosomes may participate in intercellular communication and have utility as disease biomarkers; however, little is known regarding the physiological stimuli that induce their secretion. Ca(2+) influx promotes exosome secretion, raising the possibility that exosomes are secreted during the Ca(2+)-dependent plasma membrane repair of tissues damaged by mechanical stress in vivo. To determine whether exosomes are secreted upon plasma membrane damage, we developed sensitive assays to measure exosome secretion in intact and permeabilized cells. Our results suggest that exosome secretion is coupled to Ca(2+)-dependent plasma membrane repair. We find that annexin A6 (ANXA6), a well-known plasma membrane repair protein, is recruited to MVBs in the presence of Ca(2+) and required for Ca(2+)-dependent exosome secretion, both in intact and in permeabilized cells. ANXA6 depletion stalls MVBs at the cell periphery, and ANXA6 truncations localize to different membranes, suggesting that ANXA6 may serve to tether MVBs to the plasma membrane. We find that cells secrete exosomes and other EVs upon plasma membrane damage and propose that repair-induced secretion may contribute to the pool of EVs present within biological fluids. eLife Sciences Publications, Ltd 2023-05-19 /pmc/articles/PMC10241516/ /pubmed/37204294 http://dx.doi.org/10.7554/eLife.86556 Text en © 2023, Williams, Ngo et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Williams, Justin Krish Ngo, Jordan Matthew Lehman, Isabelle Madeline Schekman, Randy Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair |
title | Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair |
title_full | Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair |
title_fullStr | Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair |
title_full_unstemmed | Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair |
title_short | Annexin A6 mediates calcium-dependent exosome secretion during plasma membrane repair |
title_sort | annexin a6 mediates calcium-dependent exosome secretion during plasma membrane repair |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241516/ https://www.ncbi.nlm.nih.gov/pubmed/37204294 http://dx.doi.org/10.7554/eLife.86556 |
work_keys_str_mv | AT williamsjustinkrish annexina6mediatescalciumdependentexosomesecretionduringplasmamembranerepair AT ngojordanmatthew annexina6mediatescalciumdependentexosomesecretionduringplasmamembranerepair AT lehmanisabellemadeline annexina6mediatescalciumdependentexosomesecretionduringplasmamembranerepair AT schekmanrandy annexina6mediatescalciumdependentexosomesecretionduringplasmamembranerepair |