Extracellular vesicles of U937 macrophage cell line infected with DENV-2 induce activation in endothelial cells EA.hy926.

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dc.contributor.authorVelandia-Romero, Myriam Lucía
dc.contributor.authorBalbás Tepedino, Arturo Gabriel
dc.contributor.authorMárquez-Ortiz, Ricaurte Alejandro
dc.contributor.authorCastellanos, Jaime
dc.contributor.authorCalderón Peláez, María Angélica
dc.contributor.authorBarreto, Alfonso
dc.contributor.authorMadroñero, Leidy Johana
dc.contributor.orcidCastellanos, Jaime [0000-0003-1596-8383]
dc.contributor.orcidVelandia-Romero, Myriam Lucía [0000-0002-3340-7304]
dc.contributor.orcidCalderón Peláez, María Angélica [0000-0003-0788-0795]
dc.date.accessioned2020-02-17T21:13:03Z
dc.date.available2020-02-17T21:13:03Z
dc.date.issued2020
dc.description.abstractenglishEndothelial activation and alteration during dengue virus (DENV) infection are multifactorial events; however, the role of extracellular vesicles (EVs) in these phenomena is not known. In the present study, we characterized the EVs released by DENV-2 infected U937 macrophage cell line and evaluated the changes in the physiology and integrity of the EA.hy926 endothelial cells exposed to them. U937 macrophages were infected, supernatants were collected, and EVs were purified and characterized. Then, polarized endothelial EA.hy926 cells were exposed to the EVs for 24 h, and the transendothelial electrical resistance (TEER), monolayer permeability, and the expression of tight junction and adhesion proteins and cytokines were evaluated. The isolated EVs from infected macrophages corresponded to exosomes and apoptotic bodies, which contained the viral NS3 protein and different miRs, among other products. Exposure of EA.hy926 cells to EVs induced an increase in TEER, as well as changes in the expression of VE-cadherin and ICAM in addition leads to an increase in TNF-α, IP-10, IL-10, RANTES, and MCP-1 secretion. These results suggest that the EVs of infected macrophages transport proteins and miR that induce early changes in the physiology of the endothelium, leading to its activation and eliciting a defense peng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0227030
dc.identifier.instnameinstname:Universidad El Bosquespa
dc.identifier.issn1932-6203
dc.identifier.reponamereponame:Repositorio Institucional Universidad El Bosquespa
dc.identifier.repourlrepourl:https://repositorio.unbosque.edu.co
dc.identifier.urihttps://hdl.handle.net/20.500.12495/1941
dc.language.isoeng
dc.publisherPlos Onespa
dc.publisher.journalPlos ONEspa
dc.relation.ispartofseriesPlos ONE, 1932-6203, Vol. 15, Nro. 1, 2020, p.1-25spa
dc.relation.urihttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0227030&type=printable
dc.rightsAttribution 4.0 International*
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.accessrightshttps://purl.org/coar/access_right/c_abf430
dc.rights.creativecommons2020
dc.rights.localAcceso abiertospa
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.decsVirus del denguespa
dc.subject.decsExosomasspa
dc.subject.decsMacrófagosspa
dc.titleExtracellular vesicles of U937 macrophage cell line infected with DENV-2 induce activation in endothelial cells EA.hy926.spa
dc.typearticlespa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersion
dc.type.localartículospa

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