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

Exploration of endogenous cardiac mitogenic factors using myocardial-specific multi-rfluorescent mice and their therapeutic application

Research Project

Project/Area Number 17K17636
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Laboratory animal science
Experimental pathology
Research InstitutionChiba University

Principal Investigator

Kanda Masato  千葉大学, 大学院医学研究院, 助教 (50444055)

Project Period (FY) 2017-04-01 – 2023-03-31
Project Status Completed (Fiscal Year 2022)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2019: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2018: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords心筋再生 / 細胞移植療法 / 心筋梗塞 / 褐色脂肪組織細胞 / 細胞移植治療 / 褐色細胞組織 / 褐色脂肪組織 / 再生促進因子
Outline of Final Research Achievements

The purpose of this study was to develop a new cell transplantation therapy for myocardial infarction, and to develop a mouse model that can detect the site of myocardial regeneration by the therapy, thereby establishing a method for the search for novel regeneration-promoting factors. Using a myocardial-specific multi-fluorescent mouse model (Rainbow-Cre mouse), we confirmed that the frequency of regeneration increased in the peri-infarct region by clonal proliferation of fluorescent myocardium in the chronic phase after myocardial infarction. Then, we developed a transplantation therapy of brown adipose tissue (BAT) cells with enhanced viability by biomaterials, and were able to confirm the trend of suppressing cardiac remodeling and preserving cardiac function. This has allowed us to establish a new transplantation therapy for myocardial infarction and a technique to specifically capture the site of accelerated proliferation at the time of cell transplantation.

Academic Significance and Societal Importance of the Research Achievements

心臓移植以外に根本的な治療法は見つかっていない慢性心筋梗塞およびそれに伴う心不全に対して、心機能を回復させる根本的治療としての再生医療の開発を目指し、拒絶反応が起こりにくい、細胞定着率の高い新しい手法を確立することができた。そして、移植治療に伴う、残存心筋由来の心筋再生頻度を正確に評価でき、増殖部位からのサンプル採取が可能なモデルを開発できたことで、新規再生促進物質を探索し、新規治療の開発につながっていくことが期待される。

Report

(7 results)
  • 2022 Annual Research Report   Final Research Report ( PDF )
  • 2021 Research-status Report
  • 2020 Research-status Report
  • 2019 Research-status Report
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (4 results)

All 2019 2018 2017

All Presentation (4 results) (of which Int'l Joint Research: 2 results)

  • [Presentation] Pulmonary Pressure Overload Stimulates Cardiac Stem Cell or Progenitor Cell-derived Cardiac Regeneration in the Right Ventricular Area2019

    • Author(s)
      神田 真人
    • Organizer
      ESC Congress 2019
    • Related Report
      2019 Research-status Report
    • Int'l Joint Research
  • [Presentation] Random Double Recombination in Rainbow-MerCreMer Mice Model can Detect Precise Frequency and Location of Cardiomyocyte-2018

    • Author(s)
      神田 真人
    • Organizer
      第82回日本循環器学会学術集会
    • Related Report
      2018 Research-status Report
  • [Presentation] Random Double Recombination in Rainbow-MerCreMer Mice Model can Detect Precise Frequency and Location of Cardiomyocyte-Derived Cardiac Regeneration after Injury2018

    • Author(s)
      神田 真人
    • Organizer
      第82回日本循環器学会学術集会
    • Related Report
      2017 Research-status Report
  • [Presentation] Endogenous Cardiomyocyte-derived Cardiac Regeneration Occurs Slowly after Myocardial Infarction and Continues into the Late Phase: Multicolor Lineage Tracing Mice Model2017

    • Author(s)
      神田 真人
    • Organizer
      ESC Congress2017
    • Related Report
      2017 Research-status Report
    • Int'l Joint Research

URL: 

Published: 2017-04-28   Modified: 2024-01-30  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi