Publication:
Isolation methods of large and small extracellular vesicles derived from cardiovascular progenitors: A comparative study.

dc.contributor.authorSaludas, Laura
dc.contributor.authorGarbayo, Elisa
dc.contributor.authorRuiz-Villalba, Adrian
dc.contributor.authorHernandez, Silvia
dc.contributor.authorVader, Pieter
dc.contributor.authorProsper, Felipe
dc.contributor.authorBlanco-Prieto, Maria J
dc.date.accessioned2023-05-03T14:56:43Z
dc.date.available2023-05-03T14:56:43Z
dc.date.issued2022-01
dc.description.abstractSince the discovery of the beneficial therapeutical effects of extracellular vesicles (EVs), these agents have been attracting great interest as next-generation therapies. EVs are nanosized membrane bodies secreted by all types of cells that mediate cell-cell communication. Although the classification of different subpopulations of EVs can be complex, they are broadly divided into microvesicles and exosomes based on their biogenesis and in large and small EVs based on their size. As this is an emerging field, current investigations are focused on basic aspects such as the more convenient method for EV isolation. In the present paper, we used cardiac progenitor cells (CPCs) to study and compare different cell culture conditions for EV isolation as well as two of the most commonly employed purification methods: ultracentrifugation (UC) and size-exclusion chromatography (SEC). Large and small EVs were separately analysed. We found that serum starvation of cells during the EV collecting period led to a dramatic decrease in EV secretion and major cell death. Regarding the isolation method, our findings suggest that UC and SEC gave similar EV recovery rates. Separation of large and small EV-enriched subpopulations was efficiently achieved with both purification protocols although certain difference in sample heterogeneity was observed. Noteworthy, while calnexin was abundant in large EVs, ALIX and CD63 were mainly found in small EVs. Finally, when the functionality of EVs was assessed on primary culture of adult murine cardiac fibroblasts, we found that EVs were taken up by these cells, which resulted in a pronounced reduction in the proliferative and migratory capacity of the cells. Specifically, a tendency towards a larger effect of SEC-related EVs was observed. No differences could be found between large and small EVs. Altogether, these results contribute to establish the basis for the use of EVs as therapeutic platforms, in particular in regenerative fields.
dc.description.versionSi
dc.identifier.citationSaludas L, Garbayo E, Ruiz-Villalba A, Hernández S, Vader P, Prósper F, et al. Isolation methods of large and small extracellular vesicles derived from cardiovascular progenitors: A comparative study. Eur J Pharm Biopharm. 2022 Jan;170:187-196.
dc.identifier.doi10.1016/j.ejpb.2021.12.012
dc.identifier.essn1873-3441
dc.identifier.pmid34968647
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.ejpb.2021.12.012
dc.identifier.urihttp://hdl.handle.net/10668/22189
dc.journal.titleEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
dc.journal.titleabbreviationEur J Pharm Biopharm
dc.language.isoen
dc.organizationCentro Andaluz de Nanomedicina y Biotecnología-BIONAND
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.page.number187-196
dc.provenanceRealizada la curación de contenido 25/09/2025.
dc.pubmedtypeComparative Study
dc.pubmedtypeJournal Article
dc.relation.publisherversionhttps://linkinghub.elsevier.com/retrieve/pii/S0939-6411(21)00361-1
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCardiovascular progenitors
dc.subjectLarge and small extracellular vesicles
dc.subjectSize-exclusion chromatography
dc.subjectUltracentrifugation
dc.subjectCentro Andaluz de Nanomedicina y Biotecnología (BIONAND)
dc.subject.meshAnimals
dc.subject.meshCalcium-Binding Proteins
dc.subject.meshCalnexin
dc.subject.meshCells, Cultured
dc.subject.meshExtracellular Vesicles
dc.subject.meshMale
dc.subject.meshMice
dc.subject.meshMyocardium
dc.subject.meshMyofibroblasts
dc.subject.meshRats, Wistar
dc.subject.meshStem Cells
dc.subject.meshTetraspanin 30
dc.titleIsolation methods of large and small extracellular vesicles derived from cardiovascular progenitors: A comparative study.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number170
dspace.entity.typePublication

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