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Engineered Surfaces That Promote Capture of Latent Proteins to Facilitate Integrin-Mediated Mechanical Activation of Growth Factors.
Dhawan, Udesh; Williams, Jonathan A; Windmill, James F C; Childs, Peter; Gonzalez-Garcia, Cristina; Dalby, Matthew J; Salmeron-Sanchez, Manuel.
Afiliação
  • Dhawan U; Centre for the Cellular Microenvironment, Mazumdar-Shaw Advanced Research Centre, University of Glasgow, Glasgow, G116EW, UK.
  • Williams JA; Department of Biomedical Engineering, Wolfson Building, University of Strathclyde, Glasgow, G4 0NW, UK.
  • Windmill JFC; Centre for Ultrasonic Engineering, Department of Electronic and Electrical Engineering, University of Strathclyde, Glasgow, G11XW, UK.
  • Childs P; Department of Biomedical Engineering, Wolfson Building, University of Strathclyde, Glasgow, G4 0NW, UK.
  • Gonzalez-Garcia C; Centre for the Cellular Microenvironment, Mazumdar-Shaw Advanced Research Centre, University of Glasgow, Glasgow, G116EW, UK.
  • Dalby MJ; Centre for the Cellular Microenvironment, Mazumdar-Shaw Advanced Research Centre, University of Glasgow, Glasgow, G116EW, UK.
  • Salmeron-Sanchez M; Centre for the Cellular Microenvironment, Mazumdar-Shaw Advanced Research Centre, University of Glasgow, Glasgow, G116EW, UK.
Adv Mater ; 36(23): e2310789, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38253339
ABSTRACT
Conventional osteogenic platforms utilize active growth factors to repair bone defects that are extensive in size, but they can adversely affect patient health. Here, an unconventional osteogenic platform is reported that functions by promoting capture of inactive osteogenic growth factor molecules to the site of cell growth for subsequent integrin-mediated activation, using a recombinant fragment of latent transforming growth factor beta-binding protein-1 (rLTBP1). It is shown that rLTBP1 binds to the growth-factor- and integrin-binding domains of fibronectin on poly(ethyl acrylate) surfaces, which immobilizes rLTBP1 and promotes the binding of latency associated peptide (LAP), within which inactive transforming growth factor beta 1 (TGF-ß1) is bound. rLTBP1 facilitates the interaction of LAP with integrin ß1 and the subsequent mechanically driven release of TGF-ß1 to stimulate canonical TGF-ß1 signaling, activating osteogenic marker expression in vitro and complete regeneration of a critical-sized bone defect in vivo.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / Fator de Crescimento Transformador beta1 Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / Fator de Crescimento Transformador beta1 Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article