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Biofabrication of endothelial cell, dermal fibroblast, and multilayered keratinocyte layers for skin tissue engineering

dc.contributor.authorBarros, Natan R [UNESP]
dc.contributor.authorKim, Han-Jun
dc.contributor.authorGouidie, Marcus J
dc.contributor.authorLee, KangJu
dc.contributor.authorBandaru, Praveen
dc.contributor.authorBanton, Ethan A
dc.contributor.authorSarikhani, Einollah
dc.contributor.authorSun, Wujin
dc.contributor.authorZhang, Shiming
dc.contributor.authorCho, Hyun-Jong
dc.contributor.authorHartel, Martin C
dc.contributor.authorOstrovidov, Serge
dc.contributor.authorAhadian, Samad
dc.contributor.authorHussain, Saber M
dc.contributor.authorAshammakhi, Nureddin
dc.contributor.authorDokmeci, Mehmet R
dc.contributor.authorHerculano, Rondinelli D [UNESP]
dc.contributor.authorLee, Junmin
dc.contributor.authorKhademhosseini, Ali
dc.contributor.institutionUniversity of California-Los Angeles
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionTerasaki Institute for Biomedical Innovation
dc.contributor.institutionThe University of Hong Kong
dc.contributor.institutionKangwon National University
dc.contributor.institutionMolecular Bioeffects Branch (USAFRL/711HPW/RHDJ)
dc.contributor.institutionMichigan State University
dc.contributor.institutionUniversity of California
dc.date.accessioned2021-06-25T10:22:20Z
dc.date.available2021-06-25T10:22:20Z
dc.date.issued2021-07-01
dc.description.abstractThe skin serves a substantial number of physiological purposes and is exposed to numerous biological and chemical agents owing to its large surface area and accessibility. Yet, current skin models are limited in emulating the multifaceted functions of skin tissues due to a lack of effort on the optimization of biomaterials and techniques at different skin layers for building skin frameworks. Here, we use biomaterial-based approaches and bioengineered techniques to develop a 3D skin model with layers of endothelial cell networks, dermal fibroblasts, and multilayered keratinocytes. Analysis of mechanical properties of gelatin methacryloyl (GelMA)-based bioinks mixed with different portions of alginate revealed bioprinted endothelium could be better modeled to optimize endothelial cell viability with a mixture of 7.5% GelMA and 2% alginate. Matrix stiffness plays a crucial role in modulating produced levels of Pro-Collagen I alpha-1 and matrix metalloproteinase-1 in human dermal fibroblasts and affecting their viability, proliferation, and spreading. Moreover, seeding human keratinocytes with gelatin-coating multiple times proved to be helpful in reducing culture time to create multiple layers of keratinocytes while maintaining their viability. The ability to fabricate selected biomaterials for each layer of skin tissues has implications in the biofabrication of skin systems for regenerative medicine and disease modeling.en
dc.description.affiliationCenter for Minimally Invasive Therapeutics (C-MIT) University of California-Los Angeles
dc.description.affiliationBioprocess and Biotechnology Department Sãao Paulo State University (Unesp) School of Pharmaceutical Sciences, Km 01 Araraquara-Jau Road
dc.description.affiliationSão Paulo State University (Unesp) Institute of Chemistry, 55 Prof. Francisco Degni Street
dc.description.affiliationTerasaki Institute for Biomedical Innovation
dc.description.affiliationDepartment of Bioengineering Henry Samueli School of Engineering and Applied Sciences University of California-Los Angeles
dc.description.affiliationDepartment of Electrical and Electronic Engineering The University of Hong Kong
dc.description.affiliationCollege of Pharmacy Kangwon National University
dc.description.affiliationU.S. Air Force Research Laboratory 711th Human Performance Wing Airman Systems Directorate Bioeffects Division Molecular Bioeffects Branch (USAFRL/711HPW/RHDJ)
dc.description.affiliationDepartment of Radiological Sciences University of California-Los Angeles
dc.description.affiliationDepartment of Biomedical Engineering Michigan State University
dc.description.affiliationDepartment of Chemical and Biomolecular Engineering Henry Samueli School of Engineering and Applied Sciences University of California-Los Angeles
dc.description.affiliationJonsson Comprehensive Cancer Centre University of California
dc.description.affiliationUnespBioprocess and Biotechnology Department Sãao Paulo State University (Unesp) School of Pharmaceutical Sciences, Km 01 Araraquara-Jau Road
dc.description.affiliationUnespSão Paulo State University (Unesp) Institute of Chemistry, 55 Prof. Francisco Degni Street
dc.identifierhttp://dx.doi.org/10.1088/1758-5090/aba503
dc.identifier.citationBiofabrication, v. 13, n. 3, 2021.
dc.identifier.doi10.1088/1758-5090/aba503
dc.identifier.issn1758-5090
dc.identifier.issn1758-5082
dc.identifier.scopus2-s2.0-85100605965
dc.identifier.urihttp://hdl.handle.net/11449/205855
dc.language.isoeng
dc.relation.ispartofBiofabrication
dc.sourceScopus
dc.subjectbioprinting
dc.subjectdermal fibroblasts,and multilayered keratinocytes
dc.subjectgelatin methacryloyl (GelMA)
dc.subjectskin tissue engineering
dc.titleBiofabrication of endothelial cell, dermal fibroblast, and multilayered keratinocyte layers for skin tissue engineeringen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0001-8689-4110[1]
unesp.author.orcid0000-0001-9238-7238[2]
unesp.author.orcid0000-0002-2692-1524[12]
unesp.author.orcid0000-0002-6784-5716[13]
unesp.author.orcid0000-0003-0181-6055[15]
unesp.author.orcid0000-0003-2226-9441[16]
unesp.author.orcid0000-0002-4414-7130[18]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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