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Tissue-engineered cartilage with inducible and tunable immunomodulatory properties
Authors:Katherine A. Glass  Jarrett M. Link  Jonathan M. Brunger  Franklin T. Moutos  Charles A. Gersbach  Farshid Guilak
Affiliation:1. Department of Orthopaedic Surgery, Duke University Medical Center, Durham, NC 27710, USA;2. Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA;3. Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA
Abstract:The pathogenesis of osteoarthritis is mediated in part by inflammatory cytokines including interleukin-1 (IL-1), which promote degradation of articular cartilage and prevent human mesenchymal stem cell (MSC) chondrogenesis. In this study, we combined gene therapy and functional tissue engineering to develop engineered cartilage with immunomodulatory properties that allow chondrogenesis in the presence of pathologic levels of IL-1 by inducing overexpression of IL-1 receptor antagonist (IL-1Ra) in MSCs via scaffold-mediated lentiviral gene delivery. A doxycycline-inducible vector was used to transduce MSCs in monolayer or within 3D woven PCL scaffolds to enable tunable IL-1Ra production. In the presence of IL-1, IL-1Ra-expressing engineered cartilage produced cartilage-specific extracellular matrix, while resisting IL-1-induced upregulation of matrix metalloproteinases and maintaining mechanical properties similar to native articular cartilage. The ability of functional engineered cartilage to deliver tunable anti-inflammatory cytokines to the joint may enhance the long-term success of therapies for cartilage injuries or osteoarthritis.
Keywords:Bioactive biomaterial   Mesenchymal stem cell   Lentivirus   Cartilage repair   Osteoarthritis   Immunoengineering
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