Screening of perfused combinatorial 3D microenvironments for cell culture

dc.contributor.authorLopes, Dianapor
dc.contributor.authorFernandes, C.por
dc.contributor.authorMiguel Nobrega, J.por
dc.contributor.authorPatricio, Sonia G.por
dc.contributor.authorOliveira, Mariana Bragapor
dc.contributor.authorMano, J. F.por
dc.date.accessioned2020-01-28T17:36:06Z
dc.date.available2020-01-28T17:36:06Z
dc.date.issued2019-09-15
dc.date.updated2020-01-28T17:18:10Z
dc.description.abstractBiomaterials combining biochemical and biophysical cues to establish close-to-extracellular matrix (ECM) models have been explored for cell expansion and differentiation purposes. Multivariate arrays are used as material-saving and rapid-to-analyze platforms, which enable selecting hit-spotted formulations targeting specific cellular responses. However, these systems often lack the ability to emulate dynamic mechanical aspects that occur in specific biological milieus and affect physiological phenomena including stem cells differentiation, tumor progression, or matrix modulation. We report a tailor-made strategy to address the combined effect of flow and biochemical composition of three-dimensional (3D) biomaterials on cellular response. We suggest a simple-to-implement device comprising (i) a perforated platform accommodating miniaturized 3D biomaterials and (ii) a bioreactor that enables the incorporation of the biomaterial-containing array into a disposable perfusion chamber. The system was upscaled to parallelizable setups, increasing the number of analyzed platforms per independent experiment. As a proof-of-concept, porous chitosan scaffolds with 1 mm diameter were functionalized with combinations of 5 ECM and cell-cell contact-mediating proteins, relevant for bone and dental regeneration, corresponding to 32 protein combinatorial formulations. Mesenchymal stem cells adhesion and production of an early osteogenic marker were assessed on-chip on static and under-flow dynamic perfusion conditions. Different hit-spotted biomaterial formulations were detected for the different flow regimes using direct image analysis. Cell-binding proteins still poorly explored as biomaterials components amelogenin and E-cadherin - were here shown as relevant cell response modulators. Their combination with ECM cell-binding proteins - fibronectin, vitronectin, and type 1 collagen - rendered specific biomaterial combinations with high cell adhesion and ALP production under flow. The developed versatile system may be targeted at wpor
dc.description.sponsorshipM.B. Oliveira acknowledges the financial support from Portuguese Foundation for Science and Technology- FCT (Grant SFRH/BPD/111354/2015). This work was developed within the scope of the projects CICECO-Aveiro Institute of Materials, POCI-01-0145-FEDER-007679 (FCT Ref. UID/CTM/50011/2013) and IPC/i3N Minho (FCT Ref. UID/CTM/50025/2013), financed by national funds through the FCT/MEC and when appropriate co-financed by FEDER under the PT2020 Partnership Agreement. This work was also supported by European Research Council grant agreement ERC-2014-ADG-669858 (project ATLAS).por
dc.distributioninternationalpor
dc.identifier.doi10.1016/j.actbio.2019.06.047por
dc.identifier.issn1742-7061por
dc.identifier.pmid31255663
dc.identifier.urihttps://hdl.handle.net/1822/63448
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147333/PTpor
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S1742706119304696?via%3Dihubpor
dc.rightsopenAccesspor
dc.subjectFlow perfusionpor
dc.subjectHigh-throughput screeningpor
dc.subject3D microenvironmentspor
dc.subjectStem cell differentiationpor
dc.subjectCell-matrix interactionspor
dc.subject.wosScience & Technology
dc.titleScreening of perfused combinatorial 3D microenvironments for cell culturepor
dc.typearticle
dspace.entity.typePublicationen
oaire.citationEndPage236por
oaire.citationStartPage222por
oaire.citationVolume96por
sdum.export.identifier5558
sdum.journalACTA BIOMATERIALIApor

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