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dc.contributor.authorLópez-Seijas, Junquera
dc.contributor.authorRey-Rico, Ana
dc.contributor.authorCarballo-Pedrares, Natalia
dc.contributor.authorMiranda-Balbuena, Diego
dc.contributor.authorLamas Criado, Ibán
dc.contributor.authorYáñez, Julián
dc.date.accessioned2024-08-06T09:32:13Z
dc.date.available2024-08-06T09:32:13Z
dc.date.issued2023
dc.identifier.citationCarballo-Pedrares, N., López-Seijas, J., Miranda-Balbuena, D., Lamas, I., Yáñez, J., & Rey-Rico, A. (2023). Gene-activated hyaluronic acid-based cryogels for cartilage tissue engineering. Journal of Controlled Release, 362, 606-619. https://doi.org/10.1016/J.JCONREL.2023.09.008es_ES
dc.identifier.urihttp://hdl.handle.net/2183/38417
dc.descriptionFinanciado para publicación en acceso aberto: Universidade da Coruña/CISUGes_ES
dc.description.abstract[Abstract] Articular cartilage injuries are very frequent lesions that if left untreated may degenerate into osteoarthritis. Gene transfer to mesenchymal stem cells (MSCs) provides a powerful approach to treat these lesions by promoting their chondrogenic differentiation into the appropriate cartilage phenotype. Non-viral vectors constitute the safest gene transfer tools, as they avoid important concerns of viral systems including immunogenicity and insertional mutagenesis. However, non-viral gene transfer usually led to lower transfection efficiencies when compared with their viral counterparts. Biomaterial-guided gene delivery has emerged as a promising alternative to increase non-viral gene transfer efficiency by achieving sustained delivery of the candidate gene into cellular microenvironment. In the present study, we designed hyaluronic acid-based gene-activated cryogels (HACGs) encapsulating a novel formulation of non-viral vectors based on niosomes (P80PX) to promote MSCs in situ transfection. The developed HACG P80PX systems showed suitable physicochemical properties to promote MSCs in situ transfection with very low cytotoxicity. Incorporation of a plasmid encoding for the transcription factor SOX9 (psox9) into HACG P80PX systems led to an effective MSCs chondrogenic differentiation with reduced expression of fibrocartilage and hypertrophic markers. The capacity of the developed systems to restore cartilage extracellular matrix was further confirmed in an ex vivo model of chondral defect.es_ES
dc.description.sponsorshipFunding: The work was supported by MICINN [RTI2018-099389-A-100, RYC2018-025617-I], Xunta de Galicia [ED431F2021/10] and Deputación da Coruña [BINV-CS/2022, 2022000021445]. Acknowledgements: We would like to acknowledge Prof. M. Cucchiarini for providing pACP-hsox9 (psox9, bp 6,915). We also thank Biobanco de A Coruña from SERGAS for providing biological samples, BASF (Ludwigshafen, Germany) for supplying the poloxamer 407 and Universidade da Coruña/CISUG for the funding for open access charge.es_ES
dc.description.sponsorshipXunta de Galicia; ED431F2021/10es_ES
dc.description.sponsorshipDeputación da Coruña; BINV-CS/2022, 2022000021445es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-099389-A-I00/ES/CRIOGELES ACTIVADOS POR GENES PARA REPARACION DE CARTILAGOes_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RYC2018-025617-I/ES/Targeted and controlled delivery systems of bioactive moleculeses_ES
dc.relation.urihttps://doi.org/10.1016/j.jconrel.2023.09.008es_ES
dc.rightsCreative Commons Attribution-Noncommercial-Noderivatives 4.0 International CC-BY-NC-NDes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCartilage repaires_ES
dc.subjectGene therapyes_ES
dc.subjectNon-viral vectorses_ES
dc.subjectNiosomeses_ES
dc.subjectP80PXes_ES
dc.subjectGene activated cryogeles_ES
dc.subjectHACGes_ES
dc.subjectMesenchymal stem cellses_ES
dc.titleGene-Activated Hyaluronic Acid-Based Cryogels for Cartilage Tissue Engineeringes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleJournal of Controlled Releasees_ES
UDC.volume362es_ES
UDC.startPage606es_ES
UDC.endPage619es_ES
dc.identifier.doi10.1016/j.jconrel.2023.09.008


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