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Spatial Growth Factor Delivery for 3D Bioprinting of Vascularized Bone with Adipose-Derived Stem/Stromal Cells as a Single Cell Source.
Goker, Meric; Derici, Utku Serhat; Gokyer, Seyda; Parmaksiz, Mehmet Goktug; Kaya, Burak; Can, Alp; Yilgor, Pinar.
Afiliação
  • Goker M; Department of Biomedical Engineering, Ankara University Faculty of Engineering, Ankara 06830, Turkey.
  • Derici US; Department of Anatomy and Regenerative Medicine, Royal College of Surgeons in Ireland, Dublin D02 YN77, Ireland.
  • Gokyer S; Department of Biomedical Engineering, Ankara University Faculty of Engineering, Ankara 06830, Turkey.
  • Parmaksiz MG; Department of Biomedical Engineering, Ankara University Faculty of Engineering, Ankara 06830, Turkey.
  • Kaya B; Department of Biomedical Engineering, Ankara University Faculty of Engineering, Ankara 06830, Turkey.
  • Can A; Department of Plastic, Reconstructive and Aesthetic Surgery, Ankara University Faculty of Medicine, Ankara 06620, Turkey.
  • Yilgor P; Ankara University Medical Design Research and Application Center, MEDITAM, Ankara 06520, Turkey.
ACS Biomater Sci Eng ; 10(3): 1607-1619, 2024 03 11.
Article em En | MEDLINE | ID: mdl-38416687
ABSTRACT
Encapsulating multiple growth factors within a scaffold enhances the regenerative capacity of engineered bone grafts through their localization and controls the spatiotemporal release profile. In this study, we bioprinted hybrid bone grafts with an inherent built-in controlled growth factor delivery system, which would contribute to vascularized bone formation using a single stem cell source, human adipose-derived stem/stromal cells (ASCs) in vitro. The strategy was to provide precise control over the ASC-derived osteogenesis and angiogenesis at certain regions of the graft through the activity of spatially positioned microencapsulated BMP-2 and VEGF within the osteogenic and angiogenic bioink during bioprinting. The 3D-bioprinted vascularized bone grafts were cultured in a perfusion bioreactor. Results proved localized expression of osteopontin and CD31 by the ASCs, which was made possible through the localized delivery activity of the built-in delivery system. In conclusion, this approach provided a methodology for generating off-the-shelf constructs for vascularized bone regeneration and has the potential to enable single-step, in situ bioprinting procedures for creating vascularized bone implants when applied to bone defects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bioimpressão Limite: Humans Idioma: En Revista: ACS Biomater Sci Eng Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Turquia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bioimpressão Limite: Humans Idioma: En Revista: ACS Biomater Sci Eng Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Turquia