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dc.contributor.authorZhou, Jing
dc.contributor.authorBenito-Martin, Alberto
dc.contributor.authorMighty, Jason
dc.contributor.authorChang, Lynne
dc.contributor.authorGhoroghi, Shima
dc.contributor.authorWu, Hao
dc.contributor.authorWong, Madeline
dc.contributor.authorGuariglia, Sara
dc.contributor.authorBaranov, Petr
dc.contributor.authorYoung, Michael
dc.contributor.authorGharbaran, Rajendra
dc.contributor.authorEmerson, Mark
dc.contributor.authorMark, Milica Tesic
dc.contributor.authorMolina, Henrik
dc.contributor.authorCanto-Solar, M Valeria
dc.contributor.authorPeinado Selgas , Hector 
dc.contributor.authorRedenti, Stephen
dc.date.accessioned2018-03-05T12:25:45Z
dc.date.available2018-03-05T12:25:45Z
dc.date.issued2018-02-12
dc.identifier.citationSci Rep. 2018;8(1):2823.es_ES
dc.identifier.issn2045-2322es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/5653
dc.description.abstractA range of cell types, including embryonic stem cells, neurons and astrocytes have been shown to release extracellular vesicles (EVs) containing molecular cargo. Across cell types, EVs facilitate transfer of mRNA, microRNA and proteins between cells. Here we describe the release kinetics and content of EVs from mouse retinal progenitor cells (mRPCs). Interestingly, mRPC derived EVs contain mRNA, miRNA and proteins associated with multipotency and retinal development. Transcripts enclosed in mRPC EVs, include the transcription factors Pax6, Hes1, and Sox2, a mitotic chromosome stabilizer Ki67, and the neural intermediate filaments Nestin and GFAP. Proteomic analysis of EV content revealed retinogenic growth factors and morphogen proteins. mRPC EVs were shown to transfer GFP mRNA between cell populations. Finally, analysis of EV mediated functional cargo delivery, using the Cre-loxP recombination system, revealed transfer and uptake of Cre+ EVs, which were then internalized by target mRPCs activating responder loxP GFP expression. In summary, the data supports a paradigm of EV genetic material encapsulation and transfer within RPC populations. RPC EV transfer may influence recipient RPC transcriptional and post-transcriptional regulation, representing a novel mechanism of differentiation and fate determination during retinal development.es_ES
dc.language.isoenges_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectROD PHOTORECEPTOR DIFFERENTIATIONes_ES
dc.subjectSTEM-CELLSes_ES
dc.subjectIN-VITROes_ES
dc.subjectGENE-EXPRESSIONes_ES
dc.subjectMESSENGER-RNAes_ES
dc.subjectFATE DETERMINATIONes_ES
dc.subjectMEDIATED TRANSFERes_ES
dc.subjectAPOPTOTIC BODIESes_ES
dc.subjectMOUSE RETINAes_ES
dc.subjectBODY-FLUIDSes_ES
dc.titleRetinal progenitor cells release extracellular vesicles containing developmental transcription factors, microRNA and membrane proteinses_ES
dc.typejournal articlees_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.identifier.pubmedID29434302es_ES
dc.format.volume8es_ES
dc.format.number1es_ES
dc.format.page2823es_ES
dc.identifier.doi10.1038/s41598-018-20421-1es_ES
dc.description.peerreviewedes_ES
dc.description.peerreviewed
dc.identifier.e-issn2045-2322es_ES
dc.relation.publisherversionhttps://10.1038/s41598-018-20421-1es_ES
dc.identifier.journalScientific reportses_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Grupos de investigaciónes_ES
dc.rights.accessRightsopen accesses_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
This item is licensed under a: Attribution-NonCommercial-NoDerivatives 4.0 Internacional