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The isolation and identification of the higher bone differentiation of mesenchymal stem cell from the pulp of human teeth and the application for the jaw bone regeneration.

Research Project

Project/Area Number 24592980
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Surgical dentistry
Research InstitutionUniversity of Tsukuba

Principal Investigator

YAMAGATA Kenji  筑波大学, 医学医療系, 講師 (00420084)

Co-Investigator(Kenkyū-buntansha) OHNEDA Osamu  筑波大学, 医学医療系, 教授 (30311872)
NAGANO Masumi  筑波大学, 医学医療系, 講師 (30436282)
Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords間葉系幹細胞 / 細胞表面マーカー / 自家移植 / 骨分化能 / Runx2 / ALP / TGF-beta
Outline of Final Research Achievements

In the crown completion stage of the dental pulp derived mesenchymal stem cells (DPSCs), the expression of the Runx2 have been increased significantly in the DPSCs of root formation stage and root completed stage from the previous time of bone differentiation induction. This result was considered due to the Runx2 stage abnormal specific expression for potential the suppression of bone differentiation. In the bone differentiation process of crown completed stage from DPSCs, expression of ALP were significantly lower form the other timing derived DPSCs. Therefore, the expression of Runx2 was analyzed for bone differentiation potential by the gene transfer of ALP to the DPSCs of crown completion. As a result, the normal bone differentiation induction was observed in the ALP gene transfer group. But it revealed that suppressing the expression of Runx2 is not observed. In the future, we will analyze a system for regulation of expression of Runx2 in DPSC.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (3 results)

All 2014 2013

All Journal Article (3 results) (of which Peer Reviewed: 3 results)

  • [Journal Article] The role of CCL5 in the ability of adipose tissue-derived mesenchymal stem cells to support repair of ischemic regions.2014

    • Author(s)
      Kimura K, Nagano M, Salazar G, Yamashita T, Tsuboi I, Mishima H, Matsushita S, Sato F, Yamagata K, Ohneda O.
    • Journal Title

      Stem Cells Dev.

      Volume: 23(5) Issue: 5 Pages: 488-501

    • DOI

      10.1089/scd.2013.0307

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Interleukin-4 receptor α-based hybrid peptide effectively induces antitumor activity in head and neck squamous cell carcinoma.2013

    • Author(s)
      Seto K, Shoda J, Horibe T, Warabi E, Ishige K, Yamagata K, Kohno M, Yanagawa T, Bukawa H, Kawakami K.
    • Journal Title

      Oncol Rep.

      Volume: 29(6) Pages: 2147-53

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Journal Article] Amelioration of cisplatin-induced nephrotoxicity in peroxiredoxin I-deficient mice.2013

    • Author(s)
      Okada K, Ma D, Warabi E, Morito N, Akiyama K, Murata Y, Yamagata K, Bukawa H, Shoda J, Ishii T, Yanagawa T.
    • Journal Title

      Cancer Chemother Pharmacol.

      Volume: 71(2) Pages: 503-9

    • Related Report
      2012 Research-status Report
    • Peer Reviewed

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Published: 2013-05-31   Modified: 2019-07-29  

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