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pubmed-article:18406458pubmed:abstractTextImplant osseointegration, defined as bone apposition and functional fixation, is a requisite for clinical success in orthopaedic and dental applications, many of which are restricted by implant loosening. Modification of implants to present bioactive motifs such as the RGD cell-adhesive sequence from fibronectin (FN) represents a promising approach in regenerative medicine. However, these biomimetic strategies have yielded only marginal enhancements in tissue healing in vivo. In this study, clinical-grade titanium implants were grafted with a non-fouling oligo(ethylene glycol)-substituted polymer coating functionalized with controlled densities of ligands of varying specificity for target integrin receptors. Biomaterials presenting the alpha5beta1-integrin-specific FN fragment FNIII 7-10 enhanced osteoblastic differentiation in bone marrow stromal cells compared to unmodified titanium and RGD-presenting surfaces. Importantly, FNIII 7-10-functionalized titanium significantly improved functional implant osseointegration compared to RGD-functionalized and unmodified titanium in vivo. This study demonstrates that bioactive coatings that promote integrin binding specificity regulate marrow-derived progenitor osteoblastic differentiation and enhance healing responses and functional integration of biomedical implants. This work identifies an innovative strategy for the rational design of biomaterials for regenerative medicine.lld:pubmed
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pubmed-article:18406458pubmed:dateRevised2011-4-1lld:pubmed
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pubmed-article:18406458pubmed:articleTitleThe effect of integrin-specific bioactive coatings on tissue healing and implant osseointegration.lld:pubmed
pubmed-article:18406458pubmed:affiliationWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, United States.lld:pubmed
pubmed-article:18406458pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18406458pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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