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Treatment for kidney disease using fetal membrane-derived mesenchymal stem cells.

Research Project

Project/Area Number 15K09256
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Kidney internal medicine
Research InstitutionAichi Medical University (2017-2018)
Nagoya University (2015-2016)

Principal Investigator

Katsuno Takayuki  愛知医科大学, 医学部, 講師 (60642337)

Co-Investigator(Kenkyū-buntansha) 丸山 彰一  名古屋大学, 医学系研究科, 教授 (10362253)
Project Period (FY) 2015-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2017: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords再生医療 / 細胞治療 / 間葉系幹細胞 / 腎臓 / 卵膜 / 低血清培養 / 卵膜由来 / 再生医学
Outline of Final Research Achievements

Applicants' previous studies have identified mesenchymal stem cells (MSC) differentiation under conditions where the serum concentration of the culture solution of fetal membrane-derived MSC (FM-MSC) was changed to 2%. However, in the low serum culture method with a serum concentration of 2%, the proliferation ability of the FN-MSCs was attenuated, and the proliferation rate was decreased in passage3. When hFGF (human fibroblast growth factor) was added for the purpose of promoting the growth of MSCs and the culture medium was introduced, an improvement in the growth rate was obtained but the problem that the undifferentiated state was not maintained became clear. The FM- MSC could not give the same result as that of adipose tissue-derived MSC. This study suggested that low serum culture may be dependent on cell source.

Academic Significance and Societal Importance of the Research Achievements

本研究は再生医療における細胞ソースとして、卵膜由来間葉系幹細胞を用いようとする点に特色がある。この際、世界に先駆け開発した低血清培養法を用いる点に独創性がある。さらに卵膜由来間葉系幹細胞を自家細胞移植だけでなく、他家細胞移植にも用いようとする点は学術的な意義がある。卵膜由来間葉系幹細胞の培養法及び治療法の確立が達成できれば、再生医療産業化の促進に期待が持たれる。

Report

(5 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • 2016 Research-status Report
  • 2015 Research-status Report
  • Research Products

    (8 results)

All 2017 2016 2015

All Journal Article (2 results) (of which Peer Reviewed: 2 results) Presentation (5 results) (of which Int'l Joint Research: 3 results) Book (1 results)

  • [Journal Article] Urinary soluble CD163 level reflects glomerular inflammation in human lupus nephritis.2016

    • Author(s)
      Endo N, Tsuboi N, Furuhashi K, Shi Y, Du Q, Abe T, Hori M, Imaizumi T, Kim H, Katsuno T, Ozaki T, Kosugi T, Matsuo S, Maruyama S.
    • Journal Title

      Nephrol Dial Transplant

      Volume: 31(12) Issue: 12 Pages: 2023-2033

    • DOI

      10.1093/ndt/gfw214

    • NAID

      120006220242

    • Related Report
      2016 Research-status Report
    • Peer Reviewed
  • [Journal Article] Transfusion of CD206+ M2 Macrophages Ameliorates Antibody-Mediated Glomerulonephritis in Mice.2016

    • Author(s)
      Du Q, Tsuboi N, Shi Y, Ito S, Sugiyama Y, Furuhashi K, Endo N, Kim H, Katsuno T, Akiyama S, Matsuo S, Isobe KI, Maruyama S.
    • Journal Title

      Am J Pathol.

      Volume: 186 Issue: 12 Pages: 3176-3188

    • DOI

      10.1016/j.ajpath.2016.08.012

    • Related Report
      2016 Research-status Report
    • Peer Reviewed
  • [Presentation] UMAN ADIPOSE-DERIVED STROMAL CELLS AMELIORATE CRESCENTIC GLOMERULONEPHRITIS2017

    • Author(s)
      Yuko Shimamura, Akimitsu Kitagawa Yutaka KamimuraYutaka Sugiyama Asuka Horinouchi Takayuki Katsuno,Naotake Tsuboi,and Shoichi Maruyama
    • Organizer
      the 18th international vasculitis & ANCA workshop
    • Place of Presentation
      東京大学(東京都文京区)
    • Year and Date
      2017-03-26
    • Related Report
      2016 Research-status Report
  • [Presentation] TLR3 Activation Enhances the Renoprotective Effect of Low Serum Cultured Adipose Derived Stromal Cell for Anti-GBM Nephritis2017

    • Author(s)
      Yutaka Kamimura, Naotake Tsuboi, Akimitsu Kitagawa, Takayuki Katsuno, Shoichi Maruyama
    • Organizer
      50th Annual Meeting of the American Society of Nephrology
    • Related Report
      2017 Research-status Report
    • Int'l Joint Research
  • [Presentation] HUMAN ADIPOSE-DERIVED STROMAL CELLS AMELIORATE CRESCENTIC GLOMERULONEPHRITIS2017

    • Author(s)
      Yuko Shimamura, Akimitsu Kitagawa Yutaka KamimuraYutaka Sugiyama Asuka Horinouchi Takayuki Katsuno,Naotake Tsuboi,and Shoichi Maruyama
    • Organizer
      the 18th international vasculitis & ANCA workshop
    • Related Report
      2017 Research-status Report
    • Int'l Joint Research
  • [Presentation] AIRED IMMUNOGLOBULIN-LIKE TYPE2 RECEPTOR ALPHA (PILRA) NEGATIVELY REGULATES MOUSE CRESCENTIC GLOMERULONEPHRITIS2017

    • Author(s)
      Yutaka Sugiyama。Naotake Tsuboi,Yuko Shimamura,Akimitsu Kitagawa, Yutaka Kamimura, Asuka HorinouchiTakayuki Katsuno,and Shoichi Maruyama
    • Organizer
      the 18th international vasculitis & ANCA workshop
    • Related Report
      2017 Research-status Report 2016 Research-status Report
    • Int'l Joint Research
  • [Presentation] anti-GBM diseaseに対する低血清培養脂肪由来幹細胞治療の有効性2015

    • Author(s)
      北川 章充、堀之内 明日花、坪井 直毅、松尾 清一、丸山 彰一
    • Organizer
      第58回日本腎臓学会学術総会
    • Place of Presentation
      名古屋国際会議場(愛知県名古屋市)
    • Year and Date
      2015-06-07
    • Related Report
      2015 Research-status Report
  • [Book] リウマチ科2016

    • Author(s)
      丸山彰一、山口真、勝野敬之、坪井直毅
    • Total Pages
      230
    • Publisher
      科学評論社
    • Related Report
      2016 Research-status Report

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Published: 2015-04-16   Modified: 2020-03-30  

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