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Reprogramming of palatal mucosa into tooth-forming epithelium

Research Project

Project/Area Number 26670848
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Dental engineering/Regenerative dentistry
Research InstitutionNiigata University

Principal Investigator

MAEDA TAKEYASU  新潟大学, 医歯学系, 教授 (40183941)

Co-Investigator(Kenkyū-buntansha) OHAZAMA Atsushi  新潟大学, 医歯学系, 教授 (40266169)
INOUE Kayoko (NOZAWA Kayoko)  新潟大学, 医歯学総合研究科, 特任准教授 (90303130)
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: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords口蓋皺襞 / 歯の発生 / リプログラミング
Outline of Final Research Achievements

We investigated the molecular differences between tooth and palatal rugae development in wild-type mice. In common with tooth germ cells, mesenchymal cells of the developing palatal rugae were found to be derived from the neural crest. Many tooth-related genes such as Bmp4 and Lrp4 showed expression in the palatal rugae, and signaling pathways including Bmp and Shh (which are known to regulate tooth development) were also activated during palatal rugae formation. However, expression of several tooth-related molecules including Msx1 could not be detected within the developing palatal rugae. Transgenic mice with altered expression of the molecules found in the developing rugae exhibited highly disorganized palatal rugae.

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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