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Induction of tendon/ligament progenitor cells from human iPSCs

Research Project

Project/Area Number 16K15664
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Orthopaedic surgery
Research InstitutionKyoto University

Principal Investigator

ALEV CANTAS  京都大学, iPS細胞研究所, 特定拠点助教 (30726477)

Co-Investigator(Kenkyū-buntansha) 池谷 真  京都大学, iPS細胞研究所, 准教授 (20442923)
Co-Investigator(Renkei-kenkyūsha) WOLTJEN Knut  京都大学, iPS細胞研究所, 准教授 (50589489)
TOGUCHIDA Junya  京都大学, ウイルス・再生医科学研究所, 教授 (40273502)
SHENG Guo jun  熊本大学, 国際先端医学研究機構, 教授 (20399439)
Project Period (FY) 2016-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2016: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
KeywordsTendon Progenitor Cell / iPSCs / Mesoderm Differentiation / tendon progenitor cells / mesoderm differentiation / syndetome / Tendon Progenitor Cells / iPS細胞 / 腱誘導 / 中胚葉誘導 / スクレラキシス / リポーター細胞
Outline of Final Research Achievements

We succeeded to establish a step-wise in vitro induction protocol of human tendon/ligament progenitor cells (TLPCs) from iPSCs. To this end we aimed to mimic the emergence of TLPCs during embryonic development. We utilised a step-wise chemically defined feeder-free iPSC-based induction protocol of human pre-somitic and somitic mesoderm from iPSCs, followed by the in vitro induction of human syndetome cells expressing the TLPC-specific transcription factors scleraxis (SCX) and mohawk (MKX). In addition TLPCs with enthesis-like features could be also derived. These in vitro induced human tendon/ligament progenitor cells have the potential to be used for disease modelling and cellular replacement therapy.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report

URL: 

Published: 2016-04-21   Modified: 2021-12-27  

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