Please use this identifier to cite or link to this item: https://doi.org/10.1089/ten.tea.2019.0124
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dc.titleSynergistic Effect of NELL-1 and an Ultra-Low Dose of BMP-2 on Spinal Fusion
dc.contributor.authorLiu, L
dc.contributor.authorLam, WMR
dc.contributor.authorNaidu, M
dc.contributor.authorYang, Z
dc.contributor.authorWang, M
dc.contributor.authorRen, X
dc.contributor.authorHu, T
dc.contributor.authorKumarsing, R
dc.contributor.authorTing, K
dc.contributor.authorGoh, JCH
dc.contributor.authorWong, HK
dc.date.accessioned2020-12-02T04:58:15Z
dc.date.available2020-12-02T04:58:15Z
dc.date.issued2019-12-01
dc.identifier.citationLiu, L, Lam, WMR, Naidu, M, Yang, Z, Wang, M, Ren, X, Hu, T, Kumarsing, R, Ting, K, Goh, JCH, Wong, HK (2019-12-01). Synergistic Effect of NELL-1 and an Ultra-Low Dose of BMP-2 on Spinal Fusion. Tissue Engineering - Part A 25 (23-24) : 1677-1689. ScholarBank@NUS Repository. https://doi.org/10.1089/ten.tea.2019.0124
dc.identifier.issn19373341
dc.identifier.issn1937335X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/184421
dc.description.abstractCopyright © 2019 Mary Ann Liebert, Inc. 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.
dc.publisherMary Ann Liebert Inc
dc.sourceElements
dc.subjectNELL-1
dc.subjectcontrol release
dc.subjectdual delivery
dc.subjectpolyelectrolyte complex
dc.subjectspinal fusion
dc.subjectultra-low dose of BMP-2
dc.subjectAnimals
dc.subjectBiomechanical Phenomena
dc.subjectBone Morphogenetic Protein 2
dc.subjectCalcium-Binding Proteins
dc.subjectCell Differentiation
dc.subjectDrug Liberation
dc.subjectDrug Synergism
dc.subjectFibrinogen
dc.subjectOsteogenesis
dc.subjectPolyelectrolytes
dc.subjectRats, Sprague-Dawley
dc.subjectSpinal Fusion
dc.subjectSpine
dc.subjectSwine
dc.subjectTissue Scaffolds
dc.subjectX-Ray Microtomography
dc.typeArticle
dc.date.updated2020-08-07T03:33:46Z
dc.contributor.departmentBIOENGINEERING
dc.contributor.departmentDEPT OF BIOMEDICAL ENGINEERING
dc.contributor.departmentORTHOPAEDIC SURGERY
dc.contributor.departmentLIFE SCIENCES INSTITUTE
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.description.doi10.1089/ten.tea.2019.0124
dc.description.sourcetitleTissue Engineering - Part A
dc.description.volume25
dc.description.issue23-24
dc.description.page1677-1689
dc.published.statePublished
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