Afficher la notice abrégée

dc.rights.licenseopenen_US
dc.contributor.authorROUSSELLE, Adrien
dc.contributor.authorFERRANDON, Arielle
dc.contributor.authorMATHIEU, Eric
dc.contributor.authorGODET, Julien
dc.contributor.authorBALL, Vincent
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorCOMPERAT, Leo
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorOLIVEIRA, Hugo
dc.contributor.authorLAVALLE, Philippe
dc.contributor.authorVAUTIER, Dominique
dc.contributor.authorARNTZ, Youri
dc.date.accessioned2023-02-21T14:01:27Z
dc.date.available2023-02-21T14:01:27Z
dc.date.issued2022-12-01
dc.identifier.issn2405-8866en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172028
dc.description.abstractEnExtrusion bioprinting is a relevant 3D technology to create biological systems in regenerative medicine, pharmaceutical development and cancer research. Bioink is the necessary component to incorporate the cells that will be printed by extrusion bioprinting. However, bioinks and extrusion printing can generate shear stresses mechanically unfavorable for cell survival. We thus developed a bioink, based on methacrylated collagen and hyaluronic acid, in combination with porous poly(D,L-lactic-co-glycolic acid) solid microscaffolds to protect cells against mechanical stress during extrusion printing. We found that porosities of the microscaffolds allowed human chondosarcoma cells to colonize the structure. Moreover, metabolic activity of these chondrosarcoma cells, fibroblast cells, and dental pulp stem cells (DPSCs) incorporated within bioink (before printing) increased 4-fold in presence of a polylysine- or collagen-coated microscaffolds compared with those cultured without microscaffolds. Their survival increased by 10% either by hand deposition or by bioprinting extrusion (bioprinter BioBot®Basic) compared to cells in bioink without microscaffolds. In addition to the mechanoshield properties provided by microscaffolds, they allow the migration of DPSCs stem cells towards HCS-2/8 cancer cells after 7 days of co-culture in an organoid created by bioprinting extrusion while without microscaffolds the cells aggregated and remained static.
dc.language.isoENen_US
dc.subject.enBioink
dc.subject.enBioprinting
dc.subject.enDPSCs
dc.subject.enHCS-2/8
dc.subject.enMicroscaffolds
dc.subject.enOrganoids
dc.title.enEnhancing cell survival in 3D printing of organoids using innovative bioinks loaded with pre-cellularized porous microscaffolds
dc.title.alternativeBioprintingen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.bprint.2022.e00247en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
bordeaux.journalBioprintingen_US
bordeaux.volume28en_US
bordeaux.hal.laboratoriesBioingénierie Tissulaire (BioTis) - U1026en_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
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Bioprinting&rft.date=2022-12-01&rft.volume=28&rft.eissn=2405-8866&rft.issn=2405-8866&rft.au=ROUSSELLE,%20Adrien&FERRANDON,%20Arielle&MATHIEU,%20Eric&GODET,%20Julien&BALL,%20Vincent&rft.genre=article


Fichier(s) constituant ce document

FichiersTailleFormatVue

Il n'y a pas de fichiers associés à ce document.

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée