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Disease modeling and development of therapies for Stargardt disease with PRPH2 mutations

Research Project

Project/Area Number 18K16936
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 56060:Ophthalmology-related
Research InstitutionJuntendo University

Principal Investigator

Arai Eisuke  順天堂大学, 医学部, 非常勤助教 (60568210)

Project Period (FY) 2018-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2019: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2018: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
KeywordsPRPH2 / A2E / Stargardt disease / ABCA4 / RDH12 / ER stress / 3D-retinal tissues / embryonic stem cells / 網膜変性
Outline of Final Research Achievements

We compared Prph2Rd2/wt mice, Prph2Rd2/Rd2 mice, Abac4-/- mice and WT mice at 3 weeks, 4 months and 8 months of age.
ONL was significantly thinner in Prph2Rd2/wt and Prph2Rd2/Rd2 mice than WT, suggesting that Prph2Rd2/wt and Prph2Rd2/Rd2 mice display retinal degeneration during aging. Moreover, Prph2Rd2/wt mice showed moderate degeneration compared to Prph2Rd2/Rd2 mice. We found accumulations of A2E and Lipofuscin which cause retinal degeneartion in Prph2Rd2/wt mice as well as Abac4-/- mice.
Expressions of Abca4 and Rdh12 in Prph2Rd2/wt mice were significantly reduced compared to WT. These results provide evidence that reduced Abca4 and Rdh12 expressions might contribute to accumulations of A2E and Lipofuscin in Prph2Rd2/wt mice. Expressions of ER stress markers significantly increased in Prph2Rd2/wt mice, suggesting that reduced RDH12 expressions in Prph2Rd2/wt mice might correlate with unfolded protein response.

Academic Significance and Societal Importance of the Research Achievements

Stargardt病は、構造タンパク質であるPRPH2の変異によっても発症する事がわかっているが発症機序は不明である。モデルマウスによってPRPH2変異によって発症するStargardt病もABCA4の変異のStargardt病と同様にA2Eやリポフスチンの蓄積していた。また、ABCA4とRDH12の機能異常がA2Eやリポフスチンの蓄積させる原因となっており、RDH12の機能異常には小胞体ストレス応答が関与している可能性が示唆された。
本研究によってPRPH2変異によるStargardt病の病態解明と治療法の開発につながり、学術的かつ社会的に意義が高いものであると考えられる。

Report

(3 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • Research Products

    (2 results)

All 2018

All Presentation (2 results) (of which Int'l Joint Research: 1 results)

  • [Presentation] ES細胞由来の立体網膜組織作製におけるDHAによる視細胞への分化促進2018

    • Author(s)
      新井 英介, Bhubanananda Sahu, Lindsay Perusek, Vipul M Parmar, 村上晶, 前田亜希子
    • Organizer
      第122回日本眼科学会総会
    • Related Report
      2018 Research-status Report
  • [Presentation] DHA promotes differentiation of photoreceptor cells in 3D neural retinas2018

    • Author(s)
      Eisuke Arai, Bhubanananda Sahu, Lindsay Perusek, Vipul M Parmar, Akira Murakami, Akiko Maeda
    • Organizer
      ARVO Annual Meeting 2018
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research

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Published: 2018-04-23   Modified: 2021-02-19  

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