論文

国際誌
2006年9月

Osteoinduction with highly purified beta-tricalcium phosphate in dog dorsal muscles and the proliferation of osteoclasts before heterotopic bone formation.

Biomaterials
  • Naoki Kondo
  • Akira Ogose
  • Kunihiko Tokunaga
  • Hajime Umezu
  • Katsumitsu Arai
  • Naoko Kudo
  • Makiko Hoshino
  • Hikaru Inoue
  • Hiroyuki Irie
  • Koichi Kuroda
  • Hisashi Mera
  • Naoto Endo
  • 全て表示

27
25
開始ページ
4419
終了ページ
27
記述言語
英語
掲載種別
研究論文(学術雑誌)

The aim of the study was to examine the chronological histology of osteoinduction of highly purified beta-tricalcium phosphate (beta-TCP) implanted in dog dorsal muscles. Specimens were harvested on days 14, 28, 42, 56, 112 and 168 after implantation, and were analyzed by hematoxylin and eosin (HE) staining, tartrate-resistant acid phosphatase (TRAP) staining, immunohistochemistry, in situ hybridization, and silver impregnation. After day 28, abundant TRAP- and cathepsin K-positive multinucleated cells adhered to beta-TCP, suggesting that these cells are osteoclasts that can resorb beta-TCP. On day 56, new bone was formed and alpha1 chain of type I procollagen mRNA-positive osteoblasts lined the newly formed bone. Silver impregnation showed abundant collagen fibrils within the beta-TCP micropores. These results suggest that micropores function as a storage space for extracellular matrix components, including collagen. Newly formed bone never degenerated in the late stage, suggesting that beta-TCP has good biocompatibility and this material retains the conditions appropriate for osteointegration and bioresorption. In conclusion, beta-TCP has osteoinductivity after implantation in dog dorsal muscles without use of bone marrow cells or osteoinductive cytokines. The appearance of a large number of active osteoclasts precedes new bone formation.

リンク情報
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/16690121
ID情報
  • ISSN : 0142-9612
  • PubMed ID : 16690121

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