Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.diff.2009.11.001
DC FieldValue
dc.titleBioactive nanofibers for fibroblastic differentiation of mesenchymal precursor cells for ligament/tendon tissue engineering applications
dc.contributor.authorSahoo, S.
dc.contributor.authorAng, L.-T.
dc.contributor.authorCho-Hong, Goh J.
dc.contributor.authorToh, S.-L.
dc.date.accessioned2011-08-03T01:47:29Z
dc.date.available2011-08-03T01:47:29Z
dc.date.issued2010
dc.identifier.citationSahoo, S., Ang, L.-T., Cho-Hong, Goh J., Toh, S.-L. (2010). Bioactive nanofibers for fibroblastic differentiation of mesenchymal precursor cells for ligament/tendon tissue engineering applications. Differentiation 79 (2) : 102-110. ScholarBank@NUS Repository. https://doi.org/10.1016/j.diff.2009.11.001
dc.identifier.issn03014681
dc.identifier.issn14320436
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/25275
dc.description.abstractMesenchymal stem cells and precursor cells are ideal candidates for tendon and ligament tissue engineering; however, for the stem cell-based approach to succeed, these cells would be required to proliferate and differentiate into tendon/ligament fibroblasts on the tissue engineering scaffold. Among the various fiber-based scaffolds that have been used in tendon/ligament tissue engineering, hybrid fibrous scaffolds comprising both microfibers and nanofibers have been recently shown to be particularly promising. With the nanofibrous coating presenting a biomimetic surface, the scaffolds can also potentially mimic the natural extracellular matrix in function by acting as a depot for sustained release of growth factors. In this study, we demonstrate that basic fibroblast growth factor (bFGF) could be successfully incorporated, randomly dispersed within blend-electrospun nanofibers and released in a bioactive form over 1 week. The released bioactive bFGF activated tyrosine phosphorylation signaling within seeded BMSCs. The bFGF-releasing nanofibrous scaffolds facilitated BMSC proliferation, upregulated gene expression of tendon/ligament-specific ECM proteins, increased production and deposition of collagen and tenascin-C, reduced multipotency of the BMSCs and induced tendon/ligament-like fibroblastic differentiation, indicating their potential in tendon/ligament tissue engineering applications. © 2009 International Society of Differentiation.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.diff.2009.11.001
dc.sourceScopus
dc.subjectBiomimetic scaffolds
dc.subjectBone marrow stromal cells
dc.subjectElectrospinning
dc.subjectFibroblast growth factor
dc.subjectFunctional tissue engineering
dc.subjectSustained release
dc.typeArticle
dc.contributor.departmentORTHOPAEDIC SURGERY
dc.description.doi10.1016/j.diff.2009.11.001
dc.description.sourcetitleDifferentiation
dc.description.volume79
dc.description.issue2
dc.description.page102-110
dc.identifier.isiut000283715200005
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