A microphysiological system combining electrospun fibers and electrical stimulation for the maturation of highly anisotropic cardiac tissue

dc.contributor.authorLópez Canosa, Adrián
dc.contributor.authorPérez Amodio, Soledad
dc.contributor.authorYanac-Huertas, Eduardo
dc.contributor.authorOrdoño, Jesús
dc.contributor.authorRodriguez Trujillo, Romen
dc.contributor.authorSamitier i Martí, Josep
dc.contributor.authorCastaño Linares, Óscar
dc.contributor.authorEngel, Elisabeth
dc.date.accessioned2025-03-19T18:31:04Z
dc.date.available2025-03-19T18:31:04Z
dc.date.issued2021-07-01
dc.date.updated2025-03-19T18:31:04Z
dc.description.abstractThe creation of cardiac tissue models for preclinical testing is still a non-solved problem in drug discovery, due to the limitations related to the in vitro replication of cardiac tissue complexity. Among these limitations, the difficulty of mimicking the functional properties of the myocardium due to the immaturity of the used cells hampers the obtention of reliable results that could be translated into human patients. In vivo models are the current gold standard to test new treatments, although it is widely acknowledged that the used animals are unable to fully recapitulate human physiology, which often leads to failures during clinical trials. In the present work, we present a microfluidic platform that aims to provide a range of signaling cues to immature cardiac cells to drive them towards an adult phenotype. The device combines topographical electrospun nanofibers with electrical stimulation in a microfabricated system. We validated our platform using a co-culture of neonatal mouse cardiomyocytes and cardiac fibroblasts, showing that it allows us to control the degree of anisotropy of the cardiac tissue inside the microdevice in a cost-effective way. Moreover, a 3D computational model of the electrical field was created and validated to demonstrate that our platform is able to closely match the distribution obtained with the gold standard (planar electrode technology) using inexpensive rod-shaped biocompatible stainless-steel electrodes. The functionality of the electrical stimulation was shown to induce a higher expression of the tight junction protein Cx-43, as well as the upregulation of several key genes involved in conductive and structural cardiac properties. These results validate our platform as a powerful tool for the tissue engineering community due to its low cost, high imaging compatibility, versatility, and high-throughput configuration capabilities.
dc.format.extent1 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec713651
dc.identifier.issn1758-5082
dc.identifier.urihttps://hdl.handle.net/2445/219863
dc.language.isoeng
dc.publisherInstitute of Physics Pub.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1088/1758-5090/abff12
dc.relation.ispartofBiofabrication, 2021, vol. 13, num.3
dc.relation.urihttps://doi.org/10.1088/1758-5090/abff12
dc.rights(c) Institute of Physics Pub., 2021
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Enginyeria Electrònica i Biomèdica)
dc.subject.classificationQuímica bioinorgànica
dc.subject.classificationEnginyeria de teixits
dc.subject.classificationMaterials biomèdics
dc.subject.otherBioinorganic chemistry
dc.subject.otherTissue engineering
dc.subject.otherBiomedical materials
dc.titleA microphysiological system combining electrospun fibers and electrical stimulation for the maturation of highly anisotropic cardiac tissue
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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