• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Development of PI polyamide targeting FcRg for nephritis

Research Project

Project/Area Number 24591216
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

MATSUMOTO Koichi  日本大学, 医学部, 教授 (00125064)

Co-Investigator(Kenkyū-buntansha) FUKUDA Noboru  日本大学, 総合科学研究科, 教授 (40267050)
Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
KeywordsFc受容体 / ピロール・イミダゾールポリアミド / 全身性エリテマトーデス / 腎炎 / 遺伝子治療 / 自己免疫性腎炎 / マウス
Outline of Final Research Achievements

FcRγ chain (Fecr1g) is a common intra cellular subunit of Fc receptors, which is involved in the autoimmuno diseases. We synthesized a novel gene silencer PI polyamide targeting FcRγ chain for the immunological nephritis. In in vitro experiments, the PI polyamide targeting FcRγ chain inhibited expression of FcRγ chain mRNA and FcRγ chain promoter activity in cultured J774A.1 cells. In in vivo experiments, iv administered PI polyamide targeting FcRγ chain suppressed CD16/32 positive cells. Moreover, Syc inhibitor R406 suppressed glomerulonephritis in the anti-GBM antibody-induced nephritis and lupus nephropathy in SLE model mouse. We will further develop the PI polyamides targeting FcRγ chain as potential therapeutic agents for immunological nephritis.

Report

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

    (5 results)

All 2015 2014 2013

All Presentation (5 results)

  • [Presentation] TSG-6を介したDFAT細胞移植の免疫性腎炎に対する改善効果2015

    • Author(s)
      丸山高史、福田 昇、松本太郎、渡辺めぐみ、阿部雅紀、上野高浩、遠藤守人、岡田一義、松本紘一、相馬正義、河内 裕
    • Organizer
      第14回 日本再生医療学会
    • Place of Presentation
      パシフィコ横浜(神奈川県・横浜市)
    • Year and Date
      2015-03-21
    • Related Report
      2014 Annual Research Report
  • [Presentation] 脱分化脂肪細胞(DFAT)の全身投与はTSG-6を介して免疫性糸球体腎炎を改善した2014

    • Author(s)
      丸山高史、福田 昇、渡辺めぐみ、阿部雅紀、上野高浩、松本太郎、遠藤守人、岡田一義、松本紘一、相馬正義、河内 裕
    • Organizer
      第37回 日本高血圧学会
    • Place of Presentation
      パシフィコ横浜(神奈川県・横浜市)
    • Year and Date
      2014-10-18
    • Related Report
      2014 Annual Research Report
  • [Presentation] Expression profiles of target genes of circadian clockin the kidney of spontaneously hypertensive rats2014

    • Author(s)
      Yusuke Murata, takahiro Ueno, Sho Tanaka, Noboru Fukuda, Masayoshi Soma
    • Organizer
      The 16th International SHR Symposium
    • Place of Presentation
      イタリア(ローマ)
    • Year and Date
      2014-06-17
    • Related Report
      2014 Annual Research Report
  • [Presentation] 免疫性腎炎治療薬としてのFcRγ遺伝子制御PIポリアミドのマウスへの静脈投与の効果2013

    • Author(s)
      北井真貴、梶原麻実子、上野高浩、福田 昇、羅 智靖、松本紘一、相馬正義
    • Organizer
      第56回 日本腎臓学会
    • Place of Presentation
      東京国際フォーラム(東京都千代田区)
    • Related Report
      2013 Research-status Report
  • [Presentation] Fcer1g遺伝子抑制PIポリアミドのマウスへの静脈投与による検討2013

    • Author(s)
      北井真貴、梶原麻実子、上野高浩、福田 昇、羅 智靖、松本紘一、相馬正義
    • Organizer
      第49回 高血圧関連疾患モデル学会
    • Place of Presentation
      日本大学会館(東京都千代田区)
    • Related Report
      2013 Research-status Report

URL: 

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

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi