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Bovine bone particulates containing bone anabolic factors as a potential xenogenic bone graft substitute.
Musson, David S; Gao, Ryan; Watson, Maureen; Lin, Jian-Ming; Park, Young-Eun; Tuari, Donna; Callon, Karen E; Zhu, Mark; Dalbeth, Nicola; Naot, Dorit; Munro, Jacob T; Cornish, Jillian.
Affiliation
  • Musson DS; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand. d.musson@auckland.ac.nz.
  • Gao R; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Watson M; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Lin JM; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Park YE; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Tuari D; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Callon KE; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Zhu M; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Dalbeth N; Auckland City Hospital, Auckland District Health Board, Auckland, 1023, New Zealand.
  • Naot D; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Munro JT; Department of Medicine, University of Auckland, Auckland, 1142, New Zealand.
  • Cornish J; Auckland City Hospital, Auckland District Health Board, Auckland, 1023, New Zealand.
J Orthop Surg Res ; 14(1): 60, 2019 Feb 20.
Article in En | MEDLINE | ID: mdl-30786911
BACKGROUND: Alternative grafts are needed to improve the healing of bone non-union. Here, we assessed a bovine bone product which retains the inorganic and organic components of bone, as an alternative bone graft. METHODS: Bovine bone matrix proteins (BBMPs) were isolated from bovine bone particulates (BBPs) and tested in vitro. Primary rat osteoblast viability, differentiation, and mineralisation were assessed with alamarBlue®, real-time PCR, and von Kossa staining assays, respectively. Osteoclast formation was assessed in primary murine bone marrow cultures with TRAP staining. Human osteoblast growth and differentiation in the presence of BBPs was evaluated in 3D collagen gels in vitro using alamarBlue® and real-time PCR, respectively. The efficacy of BBPs as an alternative bone graft was tested in a rat critical-size calvarial defect model, with histology scored at 4 and 12 weeks post-surgery. RESULTS: In vitro, the highest concentration of BBMPs increased mineral deposition five-fold compared to the untreated control group (P < 0.05); enhanced the expression of key osteoblast genes encoding for RUNX2, alkaline phosphatase, and osteocalcin (P < 0.05); and decreased osteoclast formation three-fold, compared to the untreated control group (P < 0.05). However, the BBPs had no effect on primary human osteoblasts in vitro, and in vivo, no difference was found in healing between the BBP-treated group and the untreated control group. CONCLUSIONS: Overall, despite the positive effects of the BBMPs on the cells of the bone, the bovine bone product as a whole did not enhance bone healing. Finding a way to harness the positive effect of these BBMPs would provide a clear benefit for healing bone non-union.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis / Bone Matrix / Bone Transplantation / Bone Substitutes / Testosterone Congeners Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: J Orthop Surg Res Year: 2019 Document type: Article Affiliation country: Nueva Zelanda Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis / Bone Matrix / Bone Transplantation / Bone Substitutes / Testosterone Congeners Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: J Orthop Surg Res Year: 2019 Document type: Article Affiliation country: Nueva Zelanda Country of publication: Reino Unido