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Analysis of the Muse cells characteristics of were obtained from dental pulp, and development of peridontal regerative therapy

Research Project

Project/Area Number 16K11844
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Periodontology
Research InstitutionTsurumi University

Principal Investigator

NAGANO Takatoshi  鶴見大学, 歯学部, 准教授 (10386914)

Co-Investigator(Kenkyū-buntansha) 金指 幹元  神奈川歯科大学, 大学院歯学研究科, 講師 (80339811)
Project Period (FY) 2016-10-21 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2018: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords歯髄 / 幹細胞 / SSEA-3 / フローサイトメトリー / 歯周組織再生療法 / 石灰化能 / Muse細胞 / 歯髄幹細胞 / 歯周組織再生 / CD-105
Outline of Final Research Achievements

Mesenchymal stem cells are known to exist in pulp tissue. However, the detailed characteristics of the stem cells have not been elucidated. Recently, the presence of novel Muse cells which has been reported. Researches mentioned that Muse cells exist in all mesenchymal tissues. However, there is hardly any report regarding the existence of Muse cells in oral tissues. Therefore, the purpose of this study was to determine the presence of Muse cells in dental pulp tissue.
About 0.5% of SSEA-3 positive cells were isolated from dental pulp cells by cell sorter. The isolated cells showed self-renewal ability in addition to expressing the genes representing the three germ layers. Furthermore, the isolated cells showed a high calcification ability when subjected to calcification-inducing medium. The results suggest that SSEA-3 positive cells derived from human dental pulp tissue are similar to Muse cells, highly capable of differentiating into osteogenic cells.

Academic Significance and Societal Importance of the Research Achievements

Muse細胞は、表面抗原であるCD105とSSEA-3の抗体を用いて二重染色後、ソーティングを行い得られるが、SSEA-3単独での分離を行った細胞でも一定程度の幹細胞が得られ、その細胞は石灰化能を有することが本研究により明らかとなった。
歯髄組織は比較的低侵襲で細胞を得ることがで可能で、便宜抜歯や智歯抜歯で得られる抜去歯は医療廃棄物であり、それらの抜去歯から歯髄組織を得ることができる。現在、主に骨髄細胞を用いた再生医療が歯科領域では行われているが、それと比較してもより低侵襲で細胞を得られるメリットがあり、今後も新たな細胞供給源として歯髄組織の有効性を検証することが期待される。

Report

(5 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • 2016 Research-status Report
  • Research Products

    (4 results)

All 2019 2018 2017

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Open Access: 2 results) Presentation (2 results)

  • [Journal Article] Characterization of SSEA-3 Positive Cells Derived from Human Dental Pulp Stem Cells2019

    • Author(s)
      Takatoshi Nagano, Taichiro Funatsu, Kazuhiro Gomi
    • Journal Title

      Journal of Hard Tissue Biology

      Volume: 28 Issue: 4 Pages: 335-340

    • DOI

      10.2485/jhtb.28.335

    • NAID

      130007738991

    • ISSN
      1341-7649, 1880-828X
    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Characterization of mesenchymal stem cells derived from periodontal ligament2018

    • Author(s)
      T. Funatsu, K. Gomi, Y. Matsushima, Y. Ujiie, T. Nagano.
    • Journal Title

      Journal of Hard Tissue Biology

      Volume: 27 Issue: 2 Pages: 131-138

    • DOI

      10.2485/jhtb.27.131

    • NAID

      130006673713

    • ISSN
      1341-7649, 1880-828X
    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] 歯髄細胞由来SSEA-3陽性細胞の特性解析2018

    • Author(s)
      長野孝俊、船津太一朗、五味一博
    • Organizer
      第149回日本歯科保存学会秋季学術大会
    • Related Report
      2018 Research-status Report
  • [Presentation] 歯根膜細胞由来SSEA-3陽性細胞の特性解析2017

    • Author(s)
      船津太一郎、松島友二、長野孝俊、五味一博
    • Organizer
      第60回春季日本歯周病学会学術大会
    • Place of Presentation
      福岡国際会議場(福岡県福岡市)
    • Year and Date
      2017-05-12
    • Related Report
      2016 Research-status Report

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Published: 2016-10-24   Modified: 2021-02-19  

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