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The Possibility that Periodontal Ligament Cells can Differentiate into Osteoblasts

Research Project

Project/Area Number 63570895
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Conservative dentistry
Research InstitutionShowa University

Principal Investigator

KOBAYASHI Makoto  Showa University, Periodontics, Lecture, 歯学部・歯周治療学, 講師 (80186767)

Co-Investigator(Kenkyū-buntansha) 野嶋 直美  昭和大学, 歯学部歯周治療学講座, 助手 (50159951)
Project Period (FY) 1988 – 1989
Project Status Completed (Fiscal Year 1990)
Budget Amount *help
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1989: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1988: ¥1,500,000 (Direct Cost: ¥1,500,000)
KeywordsPeriodontal ligament cell / Osteoblast / Alkaline phosphatase / Cyclic AMP / Osteocalcin / アルカリフォスタァターゼ活性 / 活性型ビタミンD_3
Research Abstract

Ideally, healing after periodontal therapy is the acquisition of the new connective tissue attachment with the formation of new cementum. It has been reported that periodontal ligament (PDL) cells can form new connective attachment with the production of new cementum on curretted root surface. So we examined the possibility that PDL cells can differentiate into osteoblasts and/or cementoblasts in freshly isolated PDL tissues and in cultured cells derived from PDL. PDL tissues were obtained from the incosor teeth of bovine lower jaws. Gingival connective tissues and gingival fibroblasts of the same animals were used as controls. Freshly isolated PDL tissues and cultured PDL cells showed an intense alkaline phosphatase (ALPase) activity both histochemically and biochemically. The ALPase in PDL tissues is of the bone type. The production of 3',5'-cyclic adenosine monophosphate (cAMP) was greatly increased in response to human parathyroid hormone [PTH(1-34)], in both freshly isolated PDL t … More issues and cultured PDL cells. In contrast, neither ALPase activity nor PTH-dependent cAMP production was detected in gingival connective tissues and cultured gingival fibroblasts. Furthermore, cultured PDL cells synthesized a protein immunologically cross-reactive with bovine bone gla protein (BGP), a highly reliable marker of osteoblastic cells. When 10^<-8> M la, 25-dihydroxyvitamin D_3 [la,25(OH)_2D_3] was added to the PDL cell cultures, the synthesis of the BGP-like protein was increased 2- to 3-fold. The maximal level of the synthesis was obtained 72h after the addition of la, 25(OH)_2D_3. Gingival fibroblasts cultured with or without la, 25(OH)_2D_3 did not produce any appreciable amounts of the BGP-like protein. 25-hydroxyvitamin D_3, 24R, 25-dihydroxyvitamin D_3, PTH and PGE_2 had no effect on this protein production in the cultures of PDL cells and gingival fibroblasts. These results indicate that the PDL cells have phenotypes typical of osteoblasts, indicating that they may differentiate into osteoblasts and/or cementoblasts. Less

Report

(3 results)
  • 1990 Final Research Report Summary
  • 1989 Annual Research Report
  • 1988 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] Naomi Nojima: "Fibroblastic cells derived from bovine periodontal ligaments have the phenotypes of osteoblast" Journal of Periodontal Research.

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Naomi Nojima: "Fibroblastic cells derived from bovine periodontal ligaments have the phenotypes of osteoblasts." Journal of Periodontal Research.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Naomi Nojima: "Fibroblastic cells derived from bovine periodontal ligaments have the phenotypes of osteoblasts" Journal of Periodontal Research.

    • Related Report
      1989 Annual Research Report

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Published: 1988-04-01   Modified: 2016-04-21  

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