IADR Abstract Archives

Use of recombinant amelogenin in healing of mouse calvarial defect

Background: The amelogenin protein constitutes 90% of the forming extracellular enamel matrix proteins. We have previously reported that amelogenin is expressed in cells of alveolar bone (normal and regenerating), normal long bone, cartilage and bone marrow. Later we showed that the recombinant human amelogenin protein (rHAM+) alone, produced in our laboratory, in eukaryotic system, induces the regeneration of the periodontal tissues, alveolar bone, cementum and periodontal ligament, after induction of periodontitis in the dog. We have also discovered that the spatio-temporal pattern of expression of amelogenin strongly suggests that amelogenin has an important role in normal remodeling and regeneration of bones.

Objectives: To investigate whether amelogenin has the ability to heal non-union fracture (critical size defect) in mouse calvaria (also a membranous bone).

Methods: (1) Creation of critical size defect (5 mm) in the parietal bone of the mouse. (2) Application of rHAM+ soaked in collagen sponge to the calvarial bone defect. (3) Characterization of the regenerated bone tissue 5 and 8 weeks after amelogenin application, using micro-CT analysis. (4) Use of histological, immunological and molecular biology technologies to characterize the regenerated bone tissue.

Results: Preliminary micro-CT results showed very little, if any, calvarial regeneration 5 weeks after rHAM+ application, while commencement of bone regeneration process was more clearly indicated 8 weeks after application. Micro-CT results generally concurred with the histological and immunological results.

Conclusions: Our preliminary results suggest that rHAM+ has the ability to regenerate non-union calvarial defects in the mouse. The regeneration process is indicated 8 weeks after rHAM+ application but obviously, the process initiates earlier. To achieve significant bone regeneration, for studying the pattern and mechanism involved in this regeneration process, longer periods of exposure to rHAM+ are required.

Funded by the Israeli Ministry of Health. Grant number (D.D.): 3-4064


Division: Israeli Division Meeting
Meeting: 2008 Israeli Division Meeting (Tel Aviv, Israel)
Location: Tel Aviv, Israel
Year: 2008
Final Presentation ID:
Abstract Category|Abstract Category(s): Scientific Groups
Authors
  • Sharon, Shay  ( Hebrew University, Jerusalem, N/A, Israel )
  • Gruenbaum-cohen, Yael  ( Hebrew University, Jerusalem, N/A, Israel )
  • Rosenfeld, Eli  ( Hebrew University, Jerusalem, N/A, Israel )
  • Haze, Amir  ( Hebrew University, Jerusalem, N/A, Israel )
  • Attias, Carinne  ( Hebrew University, Jerusalem, N/A, Israel )
  • Blumenfeld, Anat  ( Hebrew University, Jerusalem, N/A, Israel )
  • Deutsch, Dan  ( Hebrew University, Jerusalem, N/A, Israel )
  • SESSION INFORMATION
    Oral Session
    Craniofacial Biology