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dc.rights.licenseopenen_US
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorOLIVEIRA, Hugo
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorMÉDINA, Chantal
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorSTACHOWICZ, Marie-Laure
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorPAIVA DOS SANTOS, Bruno
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorCHAGOT, Lise
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorDUSSERRE, Nathalie
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorFRICAIN, Jean-Christophe
ORCID: 0000-0001-7855-6437
dc.date.accessioned2021-12-14T13:50:02Z
dc.date.available2021-12-14T13:50:02Z
dc.date.issued2021-06-01
dc.identifier.issn2405-8866en_US
dc.identifier.otherhttps://doi.org/10.1016/j.bprint.2021.e00134en_US
dc.identifier.urioai:crossref.org:10.1016/j.bprint.2021.e00134
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124143
dc.description.abstractEnThe field of bioprinting has shown a tremendous development in recent years, focusing on the development of advanced in vitro models and on regeneration approaches. In this scope, the lack of suitable biomaterials that can be efficiently formulated as printable bioinks, while supporting specific cellular events, is currently considered as one of the main limitations in the field. Indeed, extracellular matrix (ECM)-derived biomaterials formulated to enable printability and support cellular response, for instance via integrin binding, are eagerly awaited in the field of bioprinting. Several bioactive laminin sequences, including peptides such as YIGSR and IKVAV, have been identified to promote endothelial cell attachment and/or neurite outgrowth and guidance, respectively. Here, we show the development of two distinct bioinks, designed to foster vasculogenesis or neurogenesis, based on methacrylated collagen and hyaluronic acid (CollMA and HAMA, respectively), both relevant ECM-derived polymers, and on their combination with cysteine-flanked laminin-derived peptides. Using this strategy, it was possible to optimize the bioink printability, by tuning CollMA and HAMA concentration and ratio, and modulate their bioactivity, through adjustments in the cell-active peptide sequence spatial density, without compromising cell viability. We demonstrated that cell-specific bioinks could be customized for the bioprinting of both human umbilical vein cord endothelial cells (HUVECs) or adult rat sensory neurons from the dorsal root ganglia, and could stimulate both vasculogenesis and neurite outgrowth, respectively. This approach holds great potential as it can be tailored to other cellular models, due to its inherent capacity to accommodate different peptide compositions and to generate complex peptide mixtures and/or gradients.
dc.language.isoENen_US
dc.sourcecrossref
dc.subject.enBioink
dc.subject.enExtracellular matrix-based
dc.subject.enVasculogenesis
dc.subject.enNeurite outgrowth
dc.title.enExtracellular matrix (ECM)-derived bioinks designed to foster vasculogenesis and neurite outgrowth: Characterization and bioprinting
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.bprint.2021.e00134en_US
dc.subject.halSciences du Vivant [q-bio]/Biotechnologiesen_US
bordeaux.journalInternational Journal of Bioprintingen_US
bordeaux.pagee00134en_US
bordeaux.volume22en_US
bordeaux.hal.laboratoriesBioingénierie Tissulaire (BioTis) - UMR_S 1026en_US
bordeaux.institutionCNRSen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCHU de Bordeauxen_US
bordeaux.institutionInstitut Bergoniéen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03479756
hal.version1
hal.date.transferred2021-12-14T13:50:04Z
hal.exporttrue
workflow.import.sourcedissemin
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=International%20Journal%20of%20Bioprinting&rft.date=2021-06-01&rft.volume=22&rft.spage=e00134&rft.epage=e00134&rft.eissn=2405-8866&rft.issn=2405-8866&rft.au=OLIVEIRA,%20Hugo&M%C3%89DINA,%20Chantal&STACHOWICZ,%20Marie-Laure&PAIVA%20DOS%20SANTOS,%20Bruno&CHAGOT,%20Lise&rft.genre=article


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