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dc.rights.licenseopenen_US
dc.contributor.authorEL HAJJ, Soukaina
dc.contributor.authorNTATÉ, Martial Bankoué
dc.contributor.authorBRETON, Cyril
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorSIADOUS, Robin
dc.contributor.authorAID, Rachida
dc.contributor.authorDUPUY, Magali
dc.contributor.authorLETOURNEUR, Didier
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorAMÉDÉE, Joëlle
dc.contributor.authorDUVAL, Hervé
dc.contributor.authorDAVID, Bertrand
dc.date.accessioned2025-03-20T15:01:33Z
dc.date.available2025-03-20T15:01:33Z
dc.date.issued2024-10-18
dc.identifier.issn2310-2861en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/205585
dc.description.abstractEnUnderstanding the niche interactions between blood and bone through the in vitro co-culture of osteo-competent cells and endothelial cells is a key factor in unraveling therapeutic potentials in bone regeneration. This can be additionally supported by employing numerical simulation techniques to assess local physical factors, such as oxygen concentration, and mechanical stimuli, such as shear stress, that can mediate cellular communication. In this study, we developed a Mesenchymal Stem Cell line (MSC) and a Human Umbilical Vein Endothelial Cell line (HUVEC), which were co-cultured under flow conditions in a three-dimensional, porous, natural pullulan/dextran scaffold that was supplemented with hydroxyapatite crystals that allowed for the spontaneous formation of spheroids. After 2 weeks, their viability was higher under the dynamic conditions (>94%) than the static conditions (<75%), with dead cells central in the spheroids. Mineralization and collagen IV production increased under the dynamic conditions, correlating with osteogenesis and vasculogenesis. The endothelial cells clustered at the spheroidal core by day 7. Proliferation doubled in the dynamic conditions, especially at the scaffold peripheries. Lattice Boltzmann simulations showed negligible wall shear stress in the hydrogel pores but highlighted highly oxygenated zones coinciding with cell proliferation. A strong oxygen gradient likely influenced endothelial migration and cell distribution. Hypoxia was minimal, explaining high viability and spheroid maturation in the dynamic conditions. © 2024 by the authors.
dc.description.sponsorshipHydrogel poreux sous perfusion : modélisation et optimisation d'un modèle in vitro de reconstruction de défaut osseuxen_US
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enbone regeneration
dc.subject.enspheroids
dc.subject.enporous hydrogel-based scaffolds
dc.subject.enperfusion bioreactor
dc.subject.enoxygen transport
dc.subject.enspatial reorganization
dc.subject.en3D cell culture
dc.subject.enLattice Boltzmann method
dc.subject.enfluid dynamics
dc.title.enBone Spheroid Development Under Flow Conditions with Mesenchymal Stem Cells and Human Umbilical Vein Endothelial Cells in a 3D Porous Hydrogel Supplemented with Hydroxyapatite
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/gels10100666en_US
dc.subject.halSciences du Vivant [q-bio]en_US
bordeaux.journalGelsen_US
bordeaux.volume10en_US
bordeaux.hal.laboratoriesBioingénierie Tissulaire (BioTis) - U1026en_US
bordeaux.issue10en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCHU de Bordeauxen_US
bordeaux.institutionInstitut Bergoniéen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Gels&amp;rft.date=2024-10-18&amp;rft.volume=10&amp;rft.issue=10&amp;rft.eissn=2310-2861&amp;rft.issn=2310-2861&amp;rft.au=EL%20HAJJ,%20Soukaina&amp;NTAT%C3%89,%20Martial%20Bankou%C3%A9&amp;BRETON,%20Cyril&amp;SIADOUS,%20Robin&amp;AID,%20Rachida&amp;rft.genre=article


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