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dc.contributor.authorAzuaje Hualde, Enrique ORCID
dc.contributor.authorRosique, Melania
dc.contributor.authorCalatayud Sánchez, Alba ORCID
dc.contributor.authorBenito López, Fernando ORCID
dc.contributor.authorBasabe Desmonts, Lourdes ORCID
dc.contributor.authorMartínez de Pancorbo Gómez, María de los Angeles ORCID
dc.date.accessioned2021-04-17T11:54:00Z
dc.date.available2021-04-17T11:54:00Z
dc.date.issued2021-04-10
dc.identifier.citationBiotechnology and Bioengineering : (2021)es_ES
dc.identifier.issn0006-3592
dc.identifier.issn1097-0290
dc.identifier.urihttp://hdl.handle.net/10810/51055
dc.description.abstractThe effect of cell-cell contact on gene transfection is mainly unknown. Usually, transfection is carried out in batch cell cultures without control over cellular interactions, and efficiency analysis relies on complex and expensive protocols commonly involving flow cytometry as the final analytical step. Novel platforms and cell patterning are being studied in order to control cellular interactions and improve quantification methods. In this work, we report the use of surface patterning of fibronectin for the generation of two types of mesenchymal stromal cells patterns: single cell patterns without cell-to-cell contact, and small cell-colonypatterns. Both scenarios allowed the integration of the full transfection process and the continuous monitoring of thousands of individualized events by fluorescence microscopy. Our results showed that cell-to-cell contact clearly affected the transfection, as single cells presented a maximum transfection peak 6 hours earlier and had a 10 % higher transfection efficiency than cells with cell-to-cell contact.es_ES
dc.description.sponsorshipAuthors acknowledge funding support from Basque Government, under Grupos Consolidados with Grant No. IT1271-19 and from Gobierno de España, Ministerio de Economia y Competitividad, with Grant No. BIO2016-80417-P(AEI/FEDER, UE). This project has received funding from the European Union, DNASurf Horizon2020 project [#778001],funded through the Marie Sklodowska-Curie Actions RISE programme for international and intersectoral Research and Innovation Staff Exchange. E.A.-H. acknowledges funding from the BasqueGovernment, Department of Education, for predoctoral fellowship 2016. Authors thank Dr. Maite Alvarez fromtheDNA Bank Service (SGIker) of the University of the Basque Country (UPV/EHU) and European funding (ERDF and ESF)for technical and human support.Authors thank the intellectual and technical assistance from the ICTS “NANBIOSIS”, more specifically by the Drug Formulation Unit (U10) of the CIBER in Bioengineering, Biomaterials & Nanomedicine (CIBER-BBN).Authors thank Dr. Alberto Gorrochategui from “Clínica Dermatológica Ercilla (Bilbao)” for providing the hair follicles from where hHF-MSCs were extractedes_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/778001es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/BIO2016-80417-Pes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectsurface patterninges_ES
dc.subjectcell patterninges_ES
dc.subjectgene transfectiones_ES
dc.subjectcell-cellcontactes_ES
dc.subjectcontinuous monitoringes_ES
dc.subjectGFPes_ES
dc.subjectmesenchymal stromalcelles_ES
dc.titleContinuous Monitoring of Cell Transfection Efficiency with Micropatterned Substrateses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder(c) 2021 Wileyes_ES
dc.relation.publisherversionhttps://doi.org/10.1002/bit.27783es_ES
dc.identifier.doi10.1002/bit.27783
dc.contributor.funderEuropean Commission
dc.departamentoesQuímica analíticaes_ES
dc.departamentoeuKimika analitikoaes_ES


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