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Exploration of mechanisms involved in spiral artery remodeling using human induced pluripotent stem cell-derived endothelial cells

Research Project

Project/Area Number 26670720
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Obstetrics and gynecology
Research InstitutionKyoto University

Principal Investigator

Kondoh Eiji  京都大学, 医学(系)研究科(研究院), 講師 (10544950)

Co-Investigator(Kenkyū-buntansha) MOGAMI Haruta  京都大学, 大学院医学研究科, 助教 (40378766)
KONISHI Ikuo  京都大学, 大学院医学研究科, 教授 (90192062)
Co-Investigator(Renkei-kenkyūsha) SONE Masakatsu  京都大学, 大学院医学研究科, 講師 (40437207)
Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
KeywordsヒトiPS細胞 / 血管内皮細胞 / 不死化EVT / 妊娠高血圧症候群 / 母体子宮らせん動脈リモデリング不全 / iPS細胞 / リモデリング / 妊娠高血圧腎症
Outline of Final Research Achievements

Direct-contact co-culture of human induced pluripotent stem cell-derived endothelial cells adhered to immortalized extravillous trophoblast HTR-8/ SVneo cells decreased cell cell viability of human induced pluripotent stem cell-derived endothelial cells (79.7% versus 49.7%) as well as populations of CD144 positive cells.

Report

(3 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report

URL: 

Published: 2014-04-04   Modified: 2017-05-10  

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