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Biofabrication of endothelial cell, dermal fibroblast, and multilayered keratinocyte layers for skin tissue engineering.
Barros, Natan R; Kim, Han-Jun; Gouidie, Marcus J; Lee, KangJu; Bandaru, Praveen; Banton, Ethan A; Sarikhani, Einollah; Sun, Wujin; Zhang, Shiming; Cho, Hyun-Jong; Hartel, Martin C; Ostrovidov, Serge; Ahadian, Samad; Hussain, Saber M; Ashammakhi, Nureddin; Dokmeci, Mehmet R; Herculano, Rondinelli D; Lee, Junmin; Khademhosseini, Ali.
Afiliação
  • Barros NR; Center for Minimally Invasive Therapeutics (C-MIT), University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Kim HJ; Bioprocess and Biotechnology Department, Sãao Paulo State University (Unesp), School of Pharmaceutical Sciences, Km 01 Araraquara-Jau Road, Araraquara, SP 14801-902, Brazil.
  • Gouidie MJ; São Paulo State University (Unesp), Institute of Chemistry, 55 Prof. Francisco Degni Street, Araraquara, SP 14800-060, Brazil.
  • Lee K; Terasaki Institute for Biomedical Innovation, Los Angeles, CA 90064, United States of America.
  • Bandaru P; Center for Minimally Invasive Therapeutics (C-MIT), University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Banton EA; Terasaki Institute for Biomedical Innovation, Los Angeles, CA 90064, United States of America.
  • Sarikhani E; Department of Bioengineering, Henry Samueli School of Engineering and Applied Sciences, University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Sun W; Center for Minimally Invasive Therapeutics (C-MIT), University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Zhang S; Department of Bioengineering, Henry Samueli School of Engineering and Applied Sciences, University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Cho HJ; Center for Minimally Invasive Therapeutics (C-MIT), University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Hartel MC; Terasaki Institute for Biomedical Innovation, Los Angeles, CA 90064, United States of America.
  • Ostrovidov S; Department of Bioengineering, Henry Samueli School of Engineering and Applied Sciences, University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Ahadian S; Center for Minimally Invasive Therapeutics (C-MIT), University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Hussain SM; Terasaki Institute for Biomedical Innovation, Los Angeles, CA 90064, United States of America.
  • Ashammakhi N; Department of Bioengineering, Henry Samueli School of Engineering and Applied Sciences, University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Dokmeci MR; Center for Minimally Invasive Therapeutics (C-MIT), University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Herculano RD; Department of Bioengineering, Henry Samueli School of Engineering and Applied Sciences, University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Lee J; Center for Minimally Invasive Therapeutics (C-MIT), University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
  • Khademhosseini A; Department of Bioengineering, Henry Samueli School of Engineering and Applied Sciences, University of California-Los Angeles, Los Angeles, CA 90095, United States of America.
Biofabrication ; 13(3)2021 04 09.
Article em En | MEDLINE | ID: mdl-32650324
The 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Engenharia Tecidual / Bioimpressão Limite: Humans Idioma: En Revista: Biofabrication Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Engenharia Tecidual / Bioimpressão Limite: Humans Idioma: En Revista: Biofabrication Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido