DOI QR코드

DOI QR Code

The Effect of Autogenous Demineralized Dentin Matrix and Interleukin-6 on bone Regeneration

  • Jang, Won Seok (Department of Oral and Maxillofacial Surgery, School of Dentistry, Pusan National University) ;
  • Kim, Min Gu (Department of Oral and Maxillofacial Surgery, School of Dentistry, Pusan National University) ;
  • Hwang, Dae Suk (Department of Oral and Maxillofacial Surgery, School of Dentistry, Pusan National University) ;
  • Kim, Gyoo Cheon (Department of Oral Anatomy, School of Dentistry, Pusan National University) ;
  • Kim, Uk Kyu (Department of Oral and Maxillofacial Surgery, School of Dentistry, Pusan National University)
  • Received : 2017.11.21
  • Accepted : 2017.12.16
  • Published : 2017.12.31

Abstract

The aim of this study was to evaluate the role of demineralized and particulate autogenous tooth, and interleukin-6 in bone regeneration. A demineralized and particulate autogenous tooth was prepared and human osteoblast-like cells (MG63) and human osteosarcoma cells were inoculated into the culture. The rate of cell adhesion, proliferation and mineralization were examined, and the appearance of cellular attachment was observed. An 8 mm critical size defect was created in the cranium of rabbits. Nine rabbits were divided into three groups including: An experimental group A (3 rabbits), in which a demineralised and particulate autogenous tooth was grafted; an experimental group B (3 rabbits), in which a demineralized, particulate autogenous tooth was grafted in addition to interleukin-6 (20 ng/mL); and a control group. The rabbits were sacrificed at 1, 2, 4 and 6 weeks for histopathological examination with H-E and Masson's Trichrome, and immunohistochemistry with osteocalcin. The cell-based assay showed a higher rate of cell adhesion, mineralization and cellular attachment in the experimental group A compared with the control group. The animal study revealed an increased number of osteoclasts, newly formed and mature bones in the experimental group A compared with the control group. Eventually, a higher number of osteoclasts were observed in the experimental group B. However, the emergence of newly formed and mature bone was lower than in the experimental group A. The current results suggest that treatment with demineralized and particulate autogenous tooth and interleukin-6 is not effective in stimulating bone regeneration during the bone grafting procedure.

Keywords

References

  1. Chung JH, Lee JH. Study of bone healing pattern in extraction socket after application of demineralized dentin matrix material. J Korean Assoc Oral Maxillofac Surg. 2011;37:365-374. https://doi.org/10.5125/jkaoms.2011.37.5.365
  2. Yeomans JD, Urist MR. Bone induction by demineralized dentine implanted into oral, osseous and muscle tissues. Arch Oral Biol. 1967;12:999-1008. https://doi.org/10.1016/0003-9969(67)90095-7
  3. Gomes MF, Goulart MG. Densitometric analysis of the autogenous demineralized dentin matrix on the dental socket wound healing process in humans. Braz Oral Res. 2006;20:324-330. doi:10.1590/S1806-83242006000400008.
  4. Kim SG, Yeo HH, Kim YK. Grafting of large defects of the jaws with a particulate dentin-plaster of paris combination. Oral Surg Oral Pathol Oral Radiol Endod. 1999;88:22-25. doi:10.1016/S1079-2104(99)70188-5.
  5. Kim SG, Kim HK, Lim SC. Combined implantation of particulate dentin, plaster of Paris, and a bone xenograft (Bio-Oss) for bone regeneration in rats. J Cranio-Maxillofac Surg. 2001;29:282-288. doi:10.1054/jcms.2001.0236.
  6. Choi DK. Kim SG, Lim SC. The effect of particulate dentinplaster of Paris combination with/without fibrin glue in the treatment of bone defects around implants. Hosp Dent. 2007;19:120-126.
  7. Kim SG. Bone grafting using particulate dentin. Key Engineering Materials. 2007;342-343:29-32. doi:10/4028/www.scientific.net/342-343.29. https://doi.org/10.4028/www.scientific.net/KEM.342-343.29
  8. Kim YK. Scientific evidence of autogenous teeth bone graft material: Domestic literature. Dental Success. 2009;29:718-726.
  9. Kim YK. The experimental study of the implantation of toothash and plaster of paris and guided tissue regeneration using lyodura. J Korean Assoc Oral Maxillofac Surg. 1996;22:297-306.
  10. Kim SG, Kim S, Park JC. Maxillary sinus augmentation for dental implants-the use of a particulate dentin-plaster of paris combination with and without platelet-rich plasma. J Korean Maxillofac Plast Reconstr Surg. 2002;24:293-301.
  11. Na TH, Kim SG, Yoon JH, Lim SC. Effect of the bone regeneration of the mixture of human or bovine tooth-ash and the Plaster of Paris in rats. J Korean Assoc Maxillofac Plast Reconstr Surg. 2004;26:334-340.
  12. Kim SG. Bone grafting material using autogenous teeth. Daily Dental. 2010.
  13. Kang DW, Kim YK. Repair of large maxillary sinus membrane perforation using a collagen membrane: retrospective clinical study. Journal of Dental Implant Research. 2017;36:1-5
  14. Kim YK, Lee HJ, Kim KW, Kim SG, Um IW. Guide bone regeneration using autogenous teeth: case reports. J Korean Assoc Oral Maxillofac Surg. 2011;37:142-147. https://doi.org/10.5125/jkaoms.2011.37.2.142
  15. Ishimi Y, Miyaura C, Jin CH, Akatsu T, Abe E, Nakamura Y, Yamaguchi A, Yoshiki S, Matsuda T, Hirano T et al. IL-6 is produced by osteoblasts and induces bone resorption. J Immunnol. 1990;145:3297-3303.
  16. Kabashima H, Maeda K, Iwamoto Y, Hirofuh T, Yoneda M, Yamashita K, Aono M. Partial characterization of interleukin-1-like factor in human gingival crevicular fluid from patients with chronic inflammatory periodontal disease. Infect Immun. 1990:58:2621-2627.
  17. Rossomando EF, Kennedy JE, Hadjimicheal J. Tumor necrosis factor alpha in gingival crevicular fluid as a possilbe indicator of periodontal disease in humans. Arch Oral Biol. 1990:35:430-434. doi:10.1016/0003-9969(90)90205-O.
  18. Jandinski JJ. Stashenko P, Fedor LS, Leuing CC, Peros WJ, Rynar JE, Deasy MJ. Localization of interleukin-1 beta in human periodontal tissue. J Periodontal. 1991;62:36-43. doi:10.1902/jop.1991.62.1.36.
  19. Matsuki Y, Yamamoto T, Hara K. Interleukin-1 mRNA-expressing macrophage in human chronically inflamed gingival tissues. Am J Pathol. 1991;138:1299-1305.
  20. McFarlane CG, Reynolds JJ, Meikle MC. The release of interleukine-$1{\beta}$, tumor necrosis-${\alpha}$ and interferone-${\gamma}$ by cultured peripheral blood mononuclear cells from patients with periodontitis. J Periodont Res. 1990;25:207-214. doi: 10.1111/j.1600-07 65.1990.tb00906.x.
  21. Stashenko P, Jandinski JJ, Fujiyoshi P, Rynar JE, Socransky SS. Tissue levels of bone resorptive cytokines in periodeontal disease. J Periodontal. 1991;62:504-509. doi:10.1902/jop.1991.62.8.504.
  22. Thomson BM, Saklatvala J, Chamber TJ. Osteoblasts mediate interleukin-1 stimulation of bone resorption by rat osteoclasts. J Exp Med. 1986;164:104-112. https://doi.org/10.1084/jem.164.1.104
  23. Akatsu T, Takahashi N, Udagawa N, Imamura K, Yamaguchi A, Sato K, Nagata A, Suda T. Role of prostaglandins in interleukin-1 induced bone resorption in mice in vitro. J Bone Miner Res. 1991;6:183-189. doi:10.1002/jbmr.5650060212.
  24. Stashenko P, Dewhirst FE, Pero WJ, Kent RL, Ago JM. Synergistic interactions between interleukin-1, tumor necrosis factor and lymphotoxin in bone resorption. J Immunol. 1987;138:1464-1468.
  25. Thomson BM, Mundy GR, Chambers TJ. Tumor necrosis factor-${\alpha}$ and-${\beta}$ induce osteoclastic cells to stimulate osteoclastic bone resorption. J Immunol. 1987;138:775-779.
  26. Tashjian AH, Voelkel EF, Lazzaro M, Singer FR, Roberts AB, Deryrick R, Winkler ME, Levine L. ${\alpha}$ and ${\beta}$ transforming growth factors stimulate prostaglandin production and bone resorption in cultured mouse calvaria. Proc Natl Acad Sci USA. 1985;82:4535-4538. https://doi.org/10.1073/pnas.82.13.4535
  27. Tashjian AH, Hohmann EL, Antoniades NH, Levin L. Platelet derived growth factor stimulates bone resorption via prostaglandin mediated mechanism. Endocrinology. 1982;111:118-124. doi:10.1210/endo-111-1-118.
  28. Kurihara N, Bertolini D, Suda T, Akiyama Y, Roodman GD. Interleukin-6 stimulates osteoclast like multinucleated cell formation in long term human marrow cultures by inducing IL-1 release. J Immunl. 1990;144:4226-4230.
  29. Jo YW, Min WK, Park CJ, Ji HS. The clinical usefulness of biochemical markers of bone formation in patients with multiple myeloma. Annals Lab Medicine. 2005;25:285-289.
  30. Kang YH, Encyclopedia of life science. Academy. 2014.
  31. Yoshikawa Y, Peel SA, Gladstone JR, Davies JE. Biochemical analysis of the response in rat bone marrow cell cultures to mechanical stimulation, Biomed Mater Eng. 1997;7:369-377.