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3D Bioprinting of Human Adipose-Derived Stem Cells and Their Tenogenic Differentiation in Clinical-Grade Medium.
Stanco, Deborah; Boffito, Monica; Bogni, Alessia; Puricelli, Luca; Barrero, Josefa; Soldati, Gianni; Ciardelli, Gianluca.
Afiliação
  • Stanco D; Department of Mechanical and Aerospace Engineering, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin, Italy.
  • Boffito M; European Commission, Joint Research Centre (JRC), Via E. Fermi, 2749, 21027 Ispra, Italy.
  • Bogni A; Department of Mechanical and Aerospace Engineering, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Turin, Italy.
  • Puricelli L; European Commission, Joint Research Centre (JRC), Via E. Fermi, 2749, 21027 Ispra, Italy.
  • Barrero J; European Commission, Joint Research Centre (JRC), Via E. Fermi, 2749, 21027 Ispra, Italy.
  • Soldati G; European Commission, Joint Research Centre (JRC), Via E. Fermi, 2749, 21027 Ispra, Italy.
  • Ciardelli G; Swiss Stem Cell Foundation, Via in Pasquée 32, 6925 Gentilino, Switzerland.
Int J Mol Sci ; 21(22)2020 Nov 18.
Article em En | MEDLINE | ID: mdl-33218011
ABSTRACT
Defining the best combination of cells and biomaterials is a key challenge for the development of tendon tissue engineering (TE) strategies. Adipose-derived stem cells (ASCs) are ideal candidates for this purpose. In addition, controlled cell-based products adherent to good manufacturing practice (GMP) are required for their clinical scale-up. With this aim, in this study, ASC 3D bioprinting and GMP-compliant tenogenic differentiation were investigated. In detail, primary human ASCs were embedded within a nanofibrillar-cellulose/alginate bioink and 3D-bioprinted into multi-layered square-grid matrices. Bioink viscoelastic properties and scaffold ultrastructural morphology were analyzed by rheology and scanning electron microscopy (SEM). The optimal cell concentration for printing among 3, 6 and 9 × 106 ASC/mL was evaluated in terms of cell viability. ASC morphology was characterized by SEM and F-actin immunostaining. Tenogenic differentiation ability was then evaluated in terms of cell viability, morphology and expression of scleraxis and collagen type III by biochemical induction using BMP-12, TGF-ß3, CTGF and ascorbic acid supplementation (TENO). Pro-inflammatory cytokine release was also assessed. Bioprinted ASCs showed high viability and survival and exhibited a tenocyte-like phenotype after biochemical induction, with no inflammatory response to the bioink. In conclusion, we report a first proof of concept for the clinical scale-up of ASC 3D bioprinting for tendon TE.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Diferenciação Celular / Tecido Adiposo / Meios de Cultura / Bioimpressão / Impressão Tridimensional / Tenócitos Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Diferenciação Celular / Tecido Adiposo / Meios de Cultura / Bioimpressão / Impressão Tridimensional / Tenócitos Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2020 Tipo de documento: Article