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Chondrobags: A high throughput alginate-fibronectin micromass platform for in vitro human cartilage formation.
Witte, Kimia; de Andrés, María C; Wells, Julia; Dalby, Matthew J; Salmeron-Sanchez, Manuel; Oreffo, Richard O C.
Afiliação
  • Witte K; Centre for the Cellular Microenvironment, University of Glasgow, Glasgow, United Kingdom.
  • de Andrés MC; Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, United Kingdom.
  • Wells J; Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
  • Dalby MJ; INIBIC-Complexo Hospitalario Universitario A Coruña (CHUAC), Rheumatology Division, A Coruña, Spain.
  • Salmeron-Sanchez M; Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
  • Oreffo ROC; Centre for the Cellular Microenvironment, University of Glasgow, Glasgow, United Kingdom.
Biofabrication ; 12(4): 045034, 2020 10 01.
Article em En | MEDLINE | ID: mdl-33000765
ABSTRACT
The maintenance and expansion of the cells required for formation of tissue-engineered cartilage has, to date, proven difficult. This is, in part, due to the initial solid phase extracellular matrix demanded by the cells inhabiting this avascular tissue. Herein, we engineer an innovative alginate-fibronectin microfluidic-based carrier construct (termed a chondrobag) equipped with solid phase presentation of growth factors that support skeletal stem cell chondrogenic differentiation while preserving human articular chondrocyte phenotype. Results demonstrate biocompatibility, cell viability, proliferation and tissue-specific differentiation for chondrogenic markers SOX9, COL2A1 and ACAN. Modulation of chondrogenic cell hypertrophy, following culture within chondrobags loaded with TGF-ß1, was confirmed by down-regulation of hypertrophic genes COL10A1 and MMP13. MicroRNAs involved in the chondrogenesis process, including miR-140, miR-146b and miR-138 were observed. Results demonstrate the generation of a novel high-throughput, microfluidic-based, scalable carrier that supports human chondrogenesis with significant implications therein for cartilage repair-based therapies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cartilagem / Células-Tronco Mesenquimais Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cartilagem / Células-Tronco Mesenquimais Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article