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dc.contributor.authorChocarro-Wrona, Carlos
dc.contributor.authorPleguezuelos Beltrán, Paula 
dc.contributor.authorLópez de Andrés, Julia 
dc.contributor.authorAntich, Cristina
dc.contributor.authorVicente Álvarez-Manzaneda, Juan De 
dc.contributor.authorJiménez González, Gema 
dc.contributor.authorArias Santiago, Salvador Antonio 
dc.contributor.authorGálvez-Martín, Patricia
dc.contributor.authorLópez-Ruiz, Elena
dc.contributor.authorMarchal Corrales, Juan Antonio 
dc.date.accessioned2025-03-12T12:16:34Z
dc.date.available2025-03-12T12:16:34Z
dc.date.issued2025-02-20
dc.identifier.citationC. Chocarro-Wrona et al. Materials Today Bio 31 (2025) 101592 [https://doi.org/10.1016/j.mtbio.2025.101592]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/103006
dc.descriptionSupplementary data to this article can be found online at https://doi. org/10.1016/j.mtbio.2025.101592.es_ES
dc.description.abstractTo overcome the limitations of conventional skin tissue engineering (TE), 3D biofabrication approaches are being developed. However, tissue mimicry should be further improved in skin models. Here, we developed and characterized biomimetic hydrogels to obtain a biofabricated three-layered (BT) skin substitute based on the main components found in the epidermal, dermal, and hypodermal skin layers. Hydrogels for dermal and hypodermal skin layers were based on a mix of agarose and type I collagen, supplemented with skin-related extracellular matrix (ECM) components (dermatan sulfate, hyaluronic acid, and elastin) and loaded with human dermal fibroblasts (hDFs) or human mesenchymal stem/stromal cells (hMSCs), respectively. The epidermal hydrogel was formulated using type I collagen supplemented with keratin and sphingolipids, and seeded with human epidermal keratinocytes (hEKs). Physicochemical results revealed adequate viscosity, gelling times, and pH for each hydrogel solution. The BT Skin also showed good swelling and degradation kinetics, and mechanical properties in a similar range of human skin. The hydrogels and BT Skin demonstrated stable cell viability and metabolic activity, as well as intercellular communication through the release of growth factors. Moreover, the BT Skin demonstrated controlled inflammation in vivo, and produced results comparable to autografting in a mouse skin wound model. This bioactive and biomimetic three-layered BT Skin has a composition that attempts to mimic the natural ECM of the skin, formulated with the characteristic cells and biomolecules present in each skin layer, and offers promising properties for its clinical application in the treatment of patients with skin injuries.es_ES
dc.description.sponsorshipMinistry of Economy and Competitiveness, Instituto de Salud Carlos III (FEDER funds) DTS19/00143 PID2019-104883 GB-I00 TED2021-129384B-C22es_ES
dc.description.sponsorshipJunta de Andalucia P18-FR-2470 A-CTS-180-UGR20 PYC20.RE.015.UGRes_ES
dc.description.sponsorshipEuropean Union (EU) 101092269es_ES
dc.description.sponsorshipModeling Nature (MNat) QUAL21-11 DTS21/00098 B-CTS-230-UGR18es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.titleA bioactive three-layered skin substitute based on ECM components effectively promotes skin wound healing and regenerationes_ES
dc.typejournal articlees_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/HE/12345/NABIHEAL/101092269es_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.mtbio.2025.101592
dc.type.hasVersionVoRes_ES


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Atribución-NoComercial 4.0 Internacional
Except where otherwise noted, this item's license is described as Atribución-NoComercial 4.0 Internacional