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Establishment of novel diagnosis methods for hereditary nephrontubular diseases using the disease-specific iPS cells

Research Project

Project/Area Number 16K09659
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Kidney internal medicine
Research InstitutionNihon University

Principal Investigator

HAKETA Akira  日本大学, 医学部, 助教 (60624294)

Co-Investigator(Kenkyū-buntansha) 福田 昇  日本大学, 総合科学研究所, 教授 (40267050)
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2018: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords疾患特異的iPS細胞 / 遺伝性尿細管疾患 / アクアポリン / 偽性副甲状腺機能低下症 / 水 / 電解質代謝学
Outline of Final Research Achievements

To develop in vitro parathyroid hormone (PTH) stimulating test, we will establish the disease (psudehyperparathyroid: PHP)-specific iPS cells from periferal blood mononuclear cells (MNC) of PHP patients and differenciate the PHP-specific iPS cells to nephrotunular cells on which we will perform the PTH stimulating test. iPS cell line (201B7) was differenciated to nephrotunular cells in matrigel with BMP2, BMP7, activin-A and retinoic acid. 201B7 cell line was differenciated to aquaporin-positive nephrotubular cells. Addition of PTH increased cAMP levels and incorporation of Phosphorus in RPTEC. We established iPS cells from MNCs from patients with PHP and confirmed diffarenciation to aquaporin-positive nephrotubular cells. We could completely eliminate the contamination of undiffareciated iPS cells with rBC2LCN-PE23. These findings indicate possibility of establishment of diagnosis of hereditary nephrotubular diseases by the disease-specific iPS cell technology.

Academic Significance and Societal Importance of the Research Achievements

これまで遺伝性尿細管疾患、とりわけ偽性副甲状腺機能低下症の臨床的診断法であるEllsworth‐Howard試験でのPTHによる尿中cAMPとリン酸排泄の正確な評価は困難な事が多かった。今回の研究にて偽性副甲状腺機能低下症の疾患特異的iPS細胞からの培養尿細管細胞でPTH負荷によるcAMP増加とリン酸の細胞内取り込みにて、Ellsworth‐Howard試験をin vitroで行える事は大いに意義がある。予想される結果としては遺伝性尿細管疾患の正確な診断法が確立され、医療社会的意義も大きい。

Report

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

    (3 results)

All 2017

All Presentation (3 results)

  • [Presentation] iPS細胞から腎尿細管細胞への分化誘導による遺伝性腎尿細管疾患の診断法の確立2017

    • Author(s)
      田中 翔、福田 昇、松本太郎、阿部雅紀.
    • Organizer
      第16回 日本再生医療学会
    • Place of Presentation
      仙台国際センター(宮城県仙台市)
    • Year and Date
      2017-03-09
    • Related Report
      2016 Research-status Report
  • [Presentation] 疾患特異的iPS細胞を用いた偽性副甲状腺機能低下症の診断法の確立2017

    • Author(s)
      田中 翔、福田 昇、羽毛田公、小林洋樹、畑中善成、阿部雅紀、相馬正義
    • Organizer
      第90回日本内分泌学会学術総会
    • Related Report
      2017 Research-status Report
  • [Presentation] iPS細胞から腎尿細管細胞への分化誘導による偽性副甲状腺機能低下症の診断法の確立2017

    • Author(s)
      田中 翔、福田 昇、羽毛田公、小林洋樹、阿部雅紀
    • Organizer
      第60回日本腎臓学会学術総会
    • Related Report
      2017 Research-status Report

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Published: 2016-04-21   Modified: 2020-03-30  

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