Cargando…

Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells

Exosomes or small extracellular vesicles (sEVs) are membrane-bound nanoparticles that carry various macromolecules and act as autocrine and paracrine signaling messengers. In this study, sEVs from epidermoid carcinoma cells influenced by membrane presentation of the glycoprotein desmoglein 2 and its...

Descripción completa

Detalles Bibliográficos
Autores principales: Flemming, Joseph P., Hill, Brianna L., Anderson-Pullinger, Lauren, Harshyne, Larry A., Mahoney, Mỹ G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8659799/
https://www.ncbi.nlm.nih.gov/pubmed/34909749
http://dx.doi.org/10.1016/j.xjidi.2021.100053
_version_ 1784613050363412480
author Flemming, Joseph P.
Hill, Brianna L.
Anderson-Pullinger, Lauren
Harshyne, Larry A.
Mahoney, Mỹ G.
author_facet Flemming, Joseph P.
Hill, Brianna L.
Anderson-Pullinger, Lauren
Harshyne, Larry A.
Mahoney, Mỹ G.
author_sort Flemming, Joseph P.
collection PubMed
description Exosomes or small extracellular vesicles (sEVs) are membrane-bound nanoparticles that carry various macromolecules and act as autocrine and paracrine signaling messengers. In this study, sEVs from epidermoid carcinoma cells influenced by membrane presentation of the glycoprotein desmoglein 2 and its palmitoylation state were investigated. In this study, sEVs were isolated by sequential ultracentrifugation followed by iodixanol density gradient separation. They were then subjected to multiplex profiling of cytokines associated with the surface of intact sEVs. The results revealed a previously undescribed active sorting of cytokines onto the surface of low-density and high-density sEV subpopulations. Specifically, an altered surface presentation of desmoglein 2 decreased FGF-2 and VEGF in low-density sEVs. In addition, in response to desmoglein 2, IL-8 and RANTES were increased in low-density sEVs but only slightly decreased in high-density sEVs. Finally, IL-6 and G-CSF were increased dramatically in high-density sEVs. This comprehensive analysis of the cytokine production profile by squamous cell carcinoma‒derived sEVs highlights their contribution to immune evasion, pro-oncogenic and proangiogenic activity, and the potential to identify diagnostic disease biomarkers.
format Online
Article
Text
id pubmed-8659799
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-86597992021-12-13 Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells Flemming, Joseph P. Hill, Brianna L. Anderson-Pullinger, Lauren Harshyne, Larry A. Mahoney, Mỹ G. JID Innov Original Article Exosomes or small extracellular vesicles (sEVs) are membrane-bound nanoparticles that carry various macromolecules and act as autocrine and paracrine signaling messengers. In this study, sEVs from epidermoid carcinoma cells influenced by membrane presentation of the glycoprotein desmoglein 2 and its palmitoylation state were investigated. In this study, sEVs were isolated by sequential ultracentrifugation followed by iodixanol density gradient separation. They were then subjected to multiplex profiling of cytokines associated with the surface of intact sEVs. The results revealed a previously undescribed active sorting of cytokines onto the surface of low-density and high-density sEV subpopulations. Specifically, an altered surface presentation of desmoglein 2 decreased FGF-2 and VEGF in low-density sEVs. In addition, in response to desmoglein 2, IL-8 and RANTES were increased in low-density sEVs but only slightly decreased in high-density sEVs. Finally, IL-6 and G-CSF were increased dramatically in high-density sEVs. This comprehensive analysis of the cytokine production profile by squamous cell carcinoma‒derived sEVs highlights their contribution to immune evasion, pro-oncogenic and proangiogenic activity, and the potential to identify diagnostic disease biomarkers. Elsevier 2021-08-24 /pmc/articles/PMC8659799/ /pubmed/34909749 http://dx.doi.org/10.1016/j.xjidi.2021.100053 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Flemming, Joseph P.
Hill, Brianna L.
Anderson-Pullinger, Lauren
Harshyne, Larry A.
Mahoney, Mỹ G.
Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells
title Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells
title_full Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells
title_fullStr Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells
title_full_unstemmed Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells
title_short Cytokine Profiling in Low- and High-Density Small Extracellular Vesicles from Epidermoid Carcinoma Cells
title_sort cytokine profiling in low- and high-density small extracellular vesicles from epidermoid carcinoma cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8659799/
https://www.ncbi.nlm.nih.gov/pubmed/34909749
http://dx.doi.org/10.1016/j.xjidi.2021.100053
work_keys_str_mv AT flemmingjosephp cytokineprofilinginlowandhighdensitysmallextracellularvesiclesfromepidermoidcarcinomacells
AT hillbriannal cytokineprofilinginlowandhighdensitysmallextracellularvesiclesfromepidermoidcarcinomacells
AT andersonpullingerlauren cytokineprofilinginlowandhighdensitysmallextracellularvesiclesfromepidermoidcarcinomacells
AT harshynelarrya cytokineprofilinginlowandhighdensitysmallextracellularvesiclesfromepidermoidcarcinomacells
AT mahoneymyg cytokineprofilinginlowandhighdensitysmallextracellularvesiclesfromepidermoidcarcinomacells