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Engineering a 3D Vascularized Adipose Tissue Construct Using a Decellularized Lung Matrix.
DeBari, Megan K; Ng, Wai Hoe; Griffin, Mallory D; Kokai, Lauren E; Marra, Kacey G; Rubin, J Peter; Ren, Xi; Abbott, Rosalyn D.
Afiliação
  • DeBari MK; Department of Materials Science & Engineering, Carnegie Mellon University, Pittsburgh, PA 15203, USA.
  • Ng WH; Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15203, USA.
  • Griffin MD; Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15203, USA.
  • Kokai LE; Department of Plastic Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Marra KG; Department of Plastic Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Rubin JP; Department of Plastic Surgery, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Ren X; Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15203, USA.
  • Abbott RD; Department of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA 15203, USA.
Biomimetics (Basel) ; 6(3)2021 Sep 18.
Article em En | MEDLINE | ID: mdl-34562876
ABSTRACT
Critically sized defects in subcutaneous white adipose tissue result in extensive disfigurement and dysfunction and remain a reconstructive challenge for surgeons; as larger defect sizes are correlated with higher rates of complications and failure due to insufficient vascularization following implantation. Our study demonstrates, for the first time, a method to engineer perfusable, pre-vascularized, high-density adipose grafts that combine patient-derived adipose cells with a decellularized lung matrix (DLM). The lung is one of the most vascularized organs with high flow, low resistance, and a large blood-alveolar interface separated by a thin basement membrane. For our work, the large volume capacity within the alveolar compartment was repurposed for high-density adipose cell filling, while the acellular vascular bed provided efficient graft perfusion throughout. Both adipocytes and hASCs were successfully delivered and remained in the alveolar space even after weeks of culture. While adipose-derived cells maintained their morphology and functionality in both static and perfusion DLM cultures, perfusion culture offered enhanced outcomes over static culture. Furthermore, we demonstrate that endothelial cells seamlessly integrate into the acellular vascular tree of the DLM with adipocytes. These results support that the DLM is a unique platform for creating vascularized adipose tissue grafts for large defect filling.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article