Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/127412
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dc.creatorBauman, E-
dc.creatorFeijão, T-
dc.creatorCarvalho, DTO-
dc.creatorGranja, PL-
dc.creatorBarrias, CC-
dc.date.accessioned2020-06-15T10:52:11Z-
dc.date.available2020-06-15T10:52:11Z-
dc.date.issued2018-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://hdl.handle.net/10216/127412-
dc.description.abstractSpheroid culture has gained increasing popularity, arising as a promising tool for regenerative medicine applications. Importantly, spheroids may present advantages over single-cell suspensions in cell-based therapies (CT). Unfortunately, most growth media used for spheroid culture contain animal origin-components, such as fetal bovine serum (FBS). The presence of FBS compromises the safety of CT and presents economic and ethical constraints. SCC (supplement for cell culture) is a novel xeno-free (XF) industrial cell culture supplement, derived from well-controlled pooled human plasma and processed under good manufacturing practice rules. Here, we developed a XF SCC-based formulation for 2D-culture of outgrowth endothelial cells (OEC), and then used it for generating co-culture spheroids of OEC and mesenchymal stem cells (MSC). XF MSC-OEC spheroids were characterized in detail and compared to spheroids cultured in FBS-supplemented medium. XF spheroids presented comparable integrity, size and morphology as the reference culture. The use of both media resulted in spheroids with similar structure, abundant extracellular matrix deposition and specific patterns of OEC distribution and organization. Notably, XF spheroids presented significantly enhanced angiogenic potential, both in vitro (fibrin sprouting assay) and in vivo (CAM assay). These findings are particularly promising in the context of potential therapeutic applications.-
dc.description.sponsorshipThis work was supported by: i) European Regional Development Fund (ERDF) through COMPETE 2020 -Operacional Programme for Competitiveness and Internationalisation (POCI), in the framework of project NORTE-01- 0145-FEDER-000012, funded by North Portugal Regional Operational Program (Norte2020) under PORTUGAL2020 Partnership Agreement; ii) European Union 7th Framework Programme, under the Marie Curie Initial Training Programme Network IB2 (MC ITN-EID nº317052[ABP1]) (Ewa Bauman scholarship); iii) Project 3DEMT funded by POCI via FEDER (POCI-01-0145-FEDER-016627) and by FCT via OE (PTDC/BBBECT/251872014). CC Barrias acknowledges FCT for her research position FCT Investigator (IF/00296/2015). The authors acknowledge Eduardo A. Silva (UC Davis, US) for providing OEC; and i3S Scientific platforms “b.IMAGE”, “In vivo CAM assays” and “Histology and Electron Microscopy” for service providence.-
dc.language.isoeng-
dc.publisherNature Publishing Group-
dc.relation.ispartofScientific Reports, vol.8(1):230-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.meshCell Culture Techniques-
dc.subject.meshCell- and Tissue-Based Therapy / methods-
dc.subject.meshCulture Media-
dc.subject.meshEndothelial Cells / cytology-
dc.subject.meshEndothelial Cells / metabolismo-
dc.subject.meshEndothelial Cells / ultrastructure-
dc.subject.meshExtracellular Matrix-
dc.subject.meshFetal Blood / cytology-
dc.subject.meshHumans-
dc.subject.meshImmunophenotyping-
dc.subject.meshMesenchymal Stem Cells / cytology-
dc.subject.meshMesenchymal Stem Cells / metabolismo-
dc.subject.meshMesenchymal Stem Cells / ultrastructure-
dc.subject.meshSpheroids, Cellular / cytology-
dc.subject.meshSpheroids, Cellular / ultrastructure-
dc.titleXeno-free pre-vascularized spheroids for therapeutic applications-
dc.typeArtigo em Revista Científica Internacional-
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde-
dc.identifier.doi10.1038/s41598-017-18431-6-
dc.relation.publisherversionhttps://www.nature.com/articles/s41598-017-18431-6-
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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