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Augmentation of osseous phenotypes in vivo with a synthetic peptide

  • Xinhua Lin
  • , J. J. Elliot
  • , D. L. Carnes
  • , W. C. Fox
  • , L. A. Peña
  • , S. L. Campion
  • , K. Takahashi
  • , B. L. Atkinson
  • , P. O. Zamora

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

The synthetic peptide B2A2-K-NS augmented the in vitro expression of osseous phenotypes when cells were stimulated with BMP-2, an osteoinductive growth factor. B2A2-K-NS significantly enhanced the effects of BMP-2-induced alkaline phosphatase activity and mineralization. In the absence of BMP-2, B2A2-K-NS did not have an effect on these endpoints. Based on these observations, in vivo studies were conducted to evaluate if B2A2-K-NS could augment osseous phenotypes in an osteoinductive environment in which BMP-2 should be present. In one study, human demineralized bone matrix (DBM) was used to generate an osteoinductive environment and the effects of B2A2-K-NS on ectopic mineralization of subcutaneous implants evaluated. In the second study, a noncritical sized defect in rabbit ulnas with inherent reparative capacity was used as the osteoinductive environment and was treated with or without B2A2-K-NS. In the DBM studies, B2A2-K-NS augmented mineralization as determined using a combination of radiographic analysis and von Kossa staining at 4 weeks postimplant. In the rabbit ulna model, B2A2-K-NS significantly increased the radiographic bone density in the defects compared to carrier-only or no-treatment controls after 6 weeks. Histological staining confirmed that B2A2-K-NS generated a pronounced bone repair response. The results are consistent with the hypothesis that B2A2-K-NS augments osseous phenotypes in an osteoinductive environment, and suggests that B2A2-K-NS may have clinical utility.

Original languageEnglish
Pages (from-to)531-539
Number of pages9
JournalJournal of Orthopaedic Research
Volume25
Issue number4
DOIs
StatePublished - Apr 2007

Keywords

  • BMP-2
  • Bone
  • Enhancement
  • In vivo
  • Synthetic peptide

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