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Synergistic Effect of NELL-1 and an Ultra-Low Dose of BMP-2 on Spinal Fusion.
Liu, Ling; Lam, Wing Moon Raymond; Naidu, Mathanapriya; Yang, Zheng; Wang, Ming; Ren, Xiafei; Hu, Tao; Kumarsing, Ramruttun; Ting, Kang; Goh, James Cho-Hong; Wong, Hee-Kit.
Afiliação
  • Liu L; Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Lam WMR; Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Naidu M; Cancer Science Institute, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Yang Z; NUS Tissue Engineering Program (NUSTEP), Life Science Institute, National University of Singapore, Singapore, Singapore.
  • Wang M; Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Ren X; Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Hu T; Department of Spine Surgery, Shanghai East Hospital, Shanghai, China.
  • Kumarsing R; Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Ting K; Section of Orthodontics, School of Dentistry, Dental and Craniofacial Research Institute, University of California Los Angeles, Los Angeles, California.
  • Goh JC; NUS Tissue Engineering Program (NUSTEP), Life Science Institute, National University of Singapore, Singapore, Singapore.
  • Wong HK; Department of Biomedical Engineering, Faculty of Engineering, National University of Singapore, Singapore, Singapore.
Tissue Eng Part A ; 25(23-24): 1677-1689, 2019 12.
Article em En | MEDLINE | ID: mdl-31337284
Bone morphogenetic protein 2 (BMP-2) is widely used in spinal fusion but it can cause adverse effects such as ectopic bone and adipose tissue in vivo. Neural epidermal growth factor like-like molecule-1 (NELL-1) has been shown to suppress BMP-2-induced adverse effects. However, no optimum carriers that control both NELL-1 and BMP-2 releases to elicit long-term bioactivity have been developed. In this study, we employed polyelectrolyte complex (PEC) as a control release carrier for NELL-1 and BMP-2. An ultra-low dose of BMP-2 synergistically functioned with NELL-1 on bone marrow mesenchymal stem cells osteogenic differentiation with greater mineralization in vitro. The osteoinductive ability of NELL-1 and an ultra-low dose of BMP-2 in PEC was investigated in rat posterolateral spinal fusion. Our results showed increased fusion rate, bone architecture, and improved bone stiffness at 8 weeks after surgery in the combination groups compared with NELL-1 or BMP-2 alone. Moreover, the formation of ectopic bone and adipose tissue was negligible in all the PEC groups. In summary, dual delivery of NELL-1 and an ultra-low dose of BMP-2 in the PEC control release carrier has greater fusion efficiency compared with BMP-2 alone and could potentially be a better alternative to the currently used BMP-2 treatments for spinal fusion. Impact Statement In this study, polyelectrolyte complex was used to absorb neural epidermal growth factor like-like molecule-1 (NELL-1) and bone morphogenetic protein 2 (BMP-2) to achieve controlled dual release. The addition of NELL-1 significantly reduced the effective dose of BMP-2 to 2.5% of its conventional dose in absorbable collagen sponge, to produce solid spinal fusion without significant adverse effects. This study was the first to identify the efficacy of combination NELL-1 and BMP-2 in a control release carrier in spinal fusion, which could be potentially used clinically to increase fusion rate and avoid the adverse effects commonly associated with conventional BMP-2.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fusão Vertebral / Proteína Morfogenética Óssea 2 Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fusão Vertebral / Proteína Morfogenética Óssea 2 Idioma: En Ano de publicação: 2019 Tipo de documento: Article