dc.contributor.author | Azuaje Hualde, Enrique | |
dc.contributor.author | Rosique, Melania | |
dc.contributor.author | Calatayud Sánchez, Alba | |
dc.contributor.author | Benito López, Fernando | |
dc.contributor.author | Basabe Desmonts, Lourdes | |
dc.contributor.author | Martínez de Pancorbo Gómez, María de los Angeles | |
dc.date.accessioned | 2021-04-17T11:54:00Z | |
dc.date.available | 2021-04-17T11:54:00Z | |
dc.date.issued | 2021-04-10 | |
dc.identifier.citation | Biotechnology and Bioengineering : (2021) | es_ES |
dc.identifier.issn | 0006-3592 | |
dc.identifier.issn | 1097-0290 | |
dc.identifier.uri | http://hdl.handle.net/10810/51055 | |
dc.description.abstract | The 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.sponsorship | Authors 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 extracted | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Wiley | es_ES |
dc.relation | info:eu-repo/grantAgreement/EC/H2020/778001 | es_ES |
dc.relation | info:eu-repo/grantAgreement/MINECO/BIO2016-80417-P | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.subject | surface patterning | es_ES |
dc.subject | cell patterning | es_ES |
dc.subject | gene transfection | es_ES |
dc.subject | cell-cellcontact | es_ES |
dc.subject | continuous monitoring | es_ES |
dc.subject | GFP | es_ES |
dc.subject | mesenchymal stromalcell | es_ES |
dc.title | Continuous Monitoring of Cell Transfection Efficiency with Micropatterned Substrates | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.holder | (c) 2021 Wiley | es_ES |
dc.relation.publisherversion | https://doi.org/10.1002/bit.27783 | es_ES |
dc.identifier.doi | 10.1002/bit.27783 | |
dc.contributor.funder | European Commission | |
dc.departamentoes | Química analítica | es_ES |
dc.departamentoeu | Kimika analitikoa | es_ES |