Cargando…

Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology

Extracellular vesicles (EVs) mediate communication between cells and organisms across all 3 kingdoms of life. Several reports have demonstrated that EVs can transfer molecules between phylogenetically diverse species and can be used by parasites to alter the properties of the host environment. Whils...

Descripción completa

Detalles Bibliográficos
Autores principales: Simbari, Fabio, McCaskill, Jana, Coakley, Gillian, Millar, Marissa, Maizels, Rick M., Fabriás, Gemma, Casas, Josefina, Buck, Amy H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937767/
https://www.ncbi.nlm.nih.gov/pubmed/27389011
http://dx.doi.org/10.3402/jev.v5.30741
_version_ 1782441766822084608
author Simbari, Fabio
McCaskill, Jana
Coakley, Gillian
Millar, Marissa
Maizels, Rick M.
Fabriás, Gemma
Casas, Josefina
Buck, Amy H.
author_facet Simbari, Fabio
McCaskill, Jana
Coakley, Gillian
Millar, Marissa
Maizels, Rick M.
Fabriás, Gemma
Casas, Josefina
Buck, Amy H.
author_sort Simbari, Fabio
collection PubMed
description Extracellular vesicles (EVs) mediate communication between cells and organisms across all 3 kingdoms of life. Several reports have demonstrated that EVs can transfer molecules between phylogenetically diverse species and can be used by parasites to alter the properties of the host environment. Whilst the concept of vesicle secretion and uptake is broad reaching, the molecular composition of these complexes is expected to be diverse based on the physiology and environmental niche of different organisms. Exosomes are one class of EVs originally defined based on their endocytic origin, as these derive from multivesicular bodies that then fuse with the plasma membrane releasing them into the extracellular environment. The term exosome has also been used to describe any small EVs recovered by high-speed ultracentrifugation, irrespective of origin since this is not always well characterized. Here, we use comparative global lipidomic analysis to examine the composition of EVs, which we term exosomes, that are secreted by the gastrointestinal nematode, Heligmosomoides polygyrus, in relation to exosomes secreted by cells of its murine host. Ultra-performance liquid chromatography – tandem mass spectrometry (UPLC-MS/MS) analysis reveals a 9- to 62-fold enrichment of plasmalogens, as well as other classes of ether glycerophospholipids, along with a relative lack of cholesterol and sphingomyelin (SM) in the nematode exosomes compared with those secreted by murine cells. Biophysical analyses of the membrane dynamics of these exosomes demonstrate increased rigidity in those from the nematode, and parallel studies with synthetic vesicles support a role of plasmalogens in stabilizing the membrane structure. These results suggest that nematodes can maintain exosome membrane structure and integrity through increased plasmalogens, compensating for diminished levels of other lipids, including cholesterol and SM. This work also illuminates the prevalence of plasmalogens in some EVs, which has not been widely reported and could have implications for the biochemical or immunomodulatory properties of EVs. Further comparative analyses such as those described here will shed light on diversity in the molecular properties of EVs that enable them to function in cross-species communication.
format Online
Article
Text
id pubmed-4937767
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Co-Action Publishing
record_format MEDLINE/PubMed
spelling pubmed-49377672016-08-01 Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology Simbari, Fabio McCaskill, Jana Coakley, Gillian Millar, Marissa Maizels, Rick M. Fabriás, Gemma Casas, Josefina Buck, Amy H. J Extracell Vesicles Original Research Article Extracellular vesicles (EVs) mediate communication between cells and organisms across all 3 kingdoms of life. Several reports have demonstrated that EVs can transfer molecules between phylogenetically diverse species and can be used by parasites to alter the properties of the host environment. Whilst the concept of vesicle secretion and uptake is broad reaching, the molecular composition of these complexes is expected to be diverse based on the physiology and environmental niche of different organisms. Exosomes are one class of EVs originally defined based on their endocytic origin, as these derive from multivesicular bodies that then fuse with the plasma membrane releasing them into the extracellular environment. The term exosome has also been used to describe any small EVs recovered by high-speed ultracentrifugation, irrespective of origin since this is not always well characterized. Here, we use comparative global lipidomic analysis to examine the composition of EVs, which we term exosomes, that are secreted by the gastrointestinal nematode, Heligmosomoides polygyrus, in relation to exosomes secreted by cells of its murine host. Ultra-performance liquid chromatography – tandem mass spectrometry (UPLC-MS/MS) analysis reveals a 9- to 62-fold enrichment of plasmalogens, as well as other classes of ether glycerophospholipids, along with a relative lack of cholesterol and sphingomyelin (SM) in the nematode exosomes compared with those secreted by murine cells. Biophysical analyses of the membrane dynamics of these exosomes demonstrate increased rigidity in those from the nematode, and parallel studies with synthetic vesicles support a role of plasmalogens in stabilizing the membrane structure. These results suggest that nematodes can maintain exosome membrane structure and integrity through increased plasmalogens, compensating for diminished levels of other lipids, including cholesterol and SM. This work also illuminates the prevalence of plasmalogens in some EVs, which has not been widely reported and could have implications for the biochemical or immunomodulatory properties of EVs. Further comparative analyses such as those described here will shed light on diversity in the molecular properties of EVs that enable them to function in cross-species communication. Co-Action Publishing 2016-07-05 /pmc/articles/PMC4937767/ /pubmed/27389011 http://dx.doi.org/10.3402/jev.v5.30741 Text en © 2016 Fabio Simbari et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Simbari, Fabio
McCaskill, Jana
Coakley, Gillian
Millar, Marissa
Maizels, Rick M.
Fabriás, Gemma
Casas, Josefina
Buck, Amy H.
Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology
title Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology
title_full Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology
title_fullStr Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology
title_full_unstemmed Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology
title_short Plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology
title_sort plasmalogen enrichment in exosomes secreted by a nematode parasite versus those derived from its mouse host: implications for exosome stability and biology
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937767/
https://www.ncbi.nlm.nih.gov/pubmed/27389011
http://dx.doi.org/10.3402/jev.v5.30741
work_keys_str_mv AT simbarifabio plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology
AT mccaskilljana plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology
AT coakleygillian plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology
AT millarmarissa plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology
AT maizelsrickm plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology
AT fabriasgemma plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology
AT casasjosefina plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology
AT buckamyh plasmalogenenrichmentinexosomessecretedbyanematodeparasiteversusthosederivedfromitsmousehostimplicationsforexosomestabilityandbiology