International Journal of Oral & Maxillofacial Surgery
Volume 27, Issue 1 , Pages 67-73, February 1998

Osteopromotive membranes enhance onlay integration and maintenance in the adult rat skull

  • Monica Gordh

      Affiliations

    • Department of Oral Surgery, Centre for Oral Health Sciences, Lund University, Malmö, Sweden
    • Address: Monica Gordh, DMD Department of Oral Surgery Centre for Oral Health Sciences Lund University S-214 21 Malmö Sweden
  • ,
  • Per Alberius

      Affiliations

    • Department of Plastic Surgery, Malmö General Hospital, Malmö, Sweden
    • Department of Oral Biochemistry, Göteborg University, Gothenburg, Sweden
  • ,
  • Olof Johnell

      Affiliations

    • Department of Orthopaedic Surgery, Malmö General Hospital, Malmö, Sweden
  • ,
  • Lisbeth Lindberg

      Affiliations

    • Department of Orthopaedic Surgery, Malmö General Hospital, Malmö, Sweden
  • ,
  • Anders Linde

      Affiliations

    • Department of Oral Biochemistry, Göteborg University, Gothenburg, Sweden

Accepted 10 August 1997.

Article Outline

Abstract 

This study aimed to evaluate the effect of an osteopromotive membrane technique on onlay bone graft survival. Unicortical bone grafts were positioned bilaterally below the temporal muscle in 21 adult Lewis rats. In 14 rats, the bone graft on the right side was covered by an expanded polytetrafluoroethylene GORE-TEX® membrane, whereas that on the left side was left uncovered. Seven rats were killed after 12 (group 1) and 20 (group 2) weeks, respectively. The remaining animals (n=7, group 3) received membranes bilaterally, of which the right-sided membrane was removed after 12 weeks, and these animals were killed after 20 weeks. The specimens were assessed by routine histology and immunohistochemical labelling for various matrix proteins. After 12 weeks (group 1), size differences between the sides were not significant, although all control onlay bone grafts microscopic signs of pronounced resorption. At 20 weeks (group 2), graft integration was more complete on the membrane side. For group 3, the height was significantly more preserved on the side where the membrane was not removed. Immunolabelling demonstrated a more intense bone remodelling at the membrane sites. Membrane treatment resulted in improved graft integration and significantly greater size persistence, but complete height was not maintained.

bone, bone grafts, artificial membrane, polytetrafluoroethylene, rats

No full text is available. To read the body of this article, please view the PDF online.

 

Back to Article Outline

References 

  1. Alberius P, Dahlin C, Linde A. Role of osteopromotion in experimental bone grafting to the skull: a study in adult rats using a membrane technique. J Oral Maxillofac Surg. 1992;50:829–834
  2. Alberius P, Gordh M, Lindberg L, Johnell O. Influence of surrounding soft tissues on onlay bone graft incorporation. Oral Surg. 1996;82:22–33
  3. Alberius P, Gordh M, Lindberg L, Johnell O. Onlay bone graft behaviour after marrow exposure of the recipient rat skull bone. Scand J Plast Reconstr Hand Surg. 1996;30:257–266
  4. Alberius P, Gordh M, Lindberg L, Johnell O. Effect of cortical perforations of both graft and host bed on onlay incorporation to the rat skull. Eur J Oral Sci. 1996;104:554–561
  5. Bengtsson E, Neame PJ, Heinegård D, Sommarin Y. The primary structure of a basic leucine-rich repeat protein, PRELP, found in connective tissues. J Biol Chem. 1995;270:25639–25644
  6. Buser D, Ruskin J, Higginbottom F, Hardwick R, Dahlin C, Schenk R. Osseointegration of titanium implants in bone regenerated in membrane-protected defects: a histologic study in the canine mandible. Int J Oral Maxillofac Implants. 1995;10:666–681
  7. Chen NT, Glowacki J, Bucky LP, Honh H-Z, Kim W-K, Yaremchuk MJ. The roles of revascularization and resorption on endurance of craniofacial onlay bone grafts in the rabbit. Plast Reconstr Surg. 1994;93:714–722
  8. Dahlin C, Andersson L, Linde A. Bone augmentation at fenestrated implants by an osteopromotive membrane technique. A controlled clinic study. Clin Oral Implant Res. 1991;2:159–165
  9. Dahlin C, Lekholm U, Linde A. Membrane induced bone augmentation at titanium implants. A report of 10 fixtures followed from 1 to 3 years after loading. Int J Periodontics Restorative Dent. 1991;11:273–281
  10. Dahlin C, Linde A, Röckert H. Stimulation of early bone formation by the combination of an osteopromotive membrane technique and hyperbaric oxygen. Scand J Reconstr Hand Surg. 1993;27:103–108
  11. Fischer LW, Termine JD, Yuong MF. Deduced protein sequence of bone small proteoglycan I (biglycan) shows homology with proteoglycan II (decorin) and several nonconnective tissue proteins in a variety of species. J Biol Chem. 1989;264:4571–4576
  12. Franzén A, Heinegård D. Isolation and characterization of two sialoproteins present only in bone calcified matrix. Biochem J. 1985;232:715–724
  13. Goldstein J, Mase C, Newman MH. Fixed membrane bone graft survival after recipient bed alteration. Plast Reconstr Surg. 1993;91:589–596
  14. Gordh M, Alberius P, Lindberg L, Johnell O. Bone graft incorporation after cortical perforations of the host bed. Otolaryngol Head Neck Surg. 1997;116:1–7
  15. Hardesty RA, Marsh JL. Craniofacial onlay bone grafting: a prospective evaluation of graft morphology, orientation, and embryonic origin. Plast Reconstr Surg. 1990;85:5–14
  16. Hedbom E, Heinegård D. Interaction of a 59-kDa connective tissue matrix protein with collagen I and collagen II. J Biol Chem. 1989;264:6898–6905
  17. Hedbom E, Antonsson P, Hjerpe A, et al. Cartilage matrix proteins. An acidic oligomeric protein (COMP) detected only in cartilage. J Biol Chem. 1992;267:6132–6134
  18. Hedner E, Linde A, Nilsson A. Systematically and locally administered growth hormone stimulates bone healing in combination with osteopromotive membranes: an experimental study in rats. J Bone Min Res. 1996;11:1952–1960
  19. Heinegård D, Björne-Persson A, Cöster L, et al. The core proteins of large and small interstitial proteoglycans from various connective tissues from distinct subgroups. Biochem J. 1985;230:181–194
  20. Heinegård D, Oldberg Å. Structure and biology of cartilage and bone matrix noncollagenous macromolecules. FASEB J. 1989;3:2042–2051
  21. Hsu S-M, Raine L, Fanger H. Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem. 1981;29:577–580
  22. Hulth A, Johnell O, Lindberg L, Heinegård D. Sequential appearance of macromolecules in bone induction in the rat. J Orthop Res. 1993;11:367–378
  23. Hunter GK, Goldberg H. Nucleation of hydroxyapatite by bone sialoprotein. In: Proc Natl Acad Sci, USA. 90:1993;p. 8562–8565
  24. Klareskog L, Forsum U, Wigren A, Wigzell H. Relationship between HLA-DR expressing cells and T-lymphocytes of different subsets in rheumatoid synovial tissue. Scand J Immunol. 1982;15:501–507
  25. Kusiak JF, Zins JE, Whitaker LA. The early revascularization of membranous bone. Plast Reconstr Surg. 1985;76:510–516
  26. LaTrenta GS, McCarthy JG, Breitbart AS, May M, Sissons HA. The role of rigid fixation in bone-augmentation of craniofacial skeleton. Plast Reconstr Surg. 1989;84:578–588
  27. Lin KY, Barlett SP, Yaremchuk MJ, Fallon M, Grossman RF, Whitaker LA. The effects of rigid fixation on the survival of onlay bone grafts: an experimental study. Plast Reconstr Surg. 1990;86:449–456
  28. Linde A, Alberius P, Dahlin C, Bjurstam K, Sundin Y. Osteopromotion: a soft tissue exclusion principle using a membrane for bone healing and bone neogenesis. J Periodontol. 1993;64:1116–1128
  29. Linde A, Hedner E. Recombinant bone morphogenetic protein-2 enhances bone healing, guided by osteopromotive e-PTFE membranes: an experimental study in rats. Calcif Tissue Int. 1995;56:549–553
  30. Nyman S, Linde J, Karring T. Reattachment—new attachment. In: Linde J editors. Textbook of clinical periodontology. Copenhagen: Munksgaard; 1988;p. 409–429
  31. Oldberg Å, Franzén A, Heinegård D. Cloning and sequence analysis of rat bone sialoprotein (osteopontin) cDNA reveals an Arg-Gly-Asp cell-binding sequence. In: Proc Natl Acad Sci, USA. 83:1986;p. 8819–8823
  32. Phillips JH, Rahn BA. Fixation effects on membranous and endochondral onlay bone-graft resorption. Plast Reconstr Surg. 1988;82:872–877
  33. Phillips JH, Rahn BA. Fixation effects on membranous and endochondral onlay bone graft revascularization and bone deposition. Plast Reconstr Surg. 1990;85:891–897
  34. Piette P, Alberius P, Samman N, Linde A. Experience with e-PTFE membrane application to bone grafting of cleft maxilla. Int J Oral Maxillofac Surg. 1995;24:327–332
  35. Poole AR, Pidoux I, Reiner A, Choiu H, Rosenberg LC. Association of an extracellular protein (chondrocalcin) with the calcification of cartilage in endochondral bone formation. J Cell Biol. 1982;98:54–62
  36. Shen Z, Heinegård D, Sommarin Y. Distribution and expression of cartilage oligomeric matrix protein and bone sialoprotein show marked changes during rat femoral head development. Matrix Biology. 1994;14:773–781
  37. part E, Extracellular matrix Timpl R, Paulsson M, Dziadek M, Fujiwara S. Basement membranes. In: Cunningham L editors. Methods in enzymology. vol. 145:Orlando, FL: Academic Press; 1988;p. 363–391
  38. Wendel M, Heinegård D, Franzén A. A major non-collagenous 62 kDa protein from rat bone mineralized matrix is identical to pp63, a phosphorylated glycoprotein from liver. Matrix. 1993;13:331–339
  39. Zellin G, Linde A. Treatment of segmental defects in long bones using osteo-promotive membranes and recombinant human bone morphogenetic protein-2. Scand J Plast Reconstr Hand Surg. 1997;30:99–106
  40. Zins JE, Whitaker LA. Membranous versus endochondral bone: implications for craniofacial reconstruction. Plast Reconstr Surg. 1983;72:778–784

PII: S0901-5027(98)80102-1

International Journal of Oral & Maxillofacial Surgery
Volume 27, Issue 1 , Pages 67-73, February 1998