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2017 Fiscal Year Final Research Report

Elucidation of matrix vesicles secretion mechanism and application to calcification

Research Project

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Project/Area Number 15K11368
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Orthodontics/Pediatric dentistry
Research InstitutionThe University of Tokushima

Principal Investigator

UEDA Kimiko (山口公子)  徳島大学, 病院, 助教 (40335807)

Co-Investigator(Kenkyū-buntansha) 岩本 勉  徳島大学, 大学院医歯薬学研究部(歯学系), 教授 (90346916)
長谷川 智一  徳島大学, 大学院医歯薬学研究部(歯学系), 講師 (50274668)
北村 尚正  徳島大学, 大学院医歯薬学研究部(歯学系), 助教 (50614020)
Project Period (FY) 2015-04-01 – 2018-03-31
Keywords硬組織形成
Outline of Final Research Achievements

Odontoblast, ameloblast, osteoblast and chondrocyte plays a role of dentin, enamel, bone and cartilage formation, respectively. However, these molecular mechanisms remain unknown that how these cells form these hard tissue. This experiment was carried out to elucidate of secretion mechanism of matrix vesicles that were secreted from hard tissue-forming cells and application to calcification, for the elucidation of the detailed molecular mechanism about hard tissue formation. Dental mesenchymal cells and dental epithelial cells differentiate into dentin-forming odontoblasts and enamel-forming ameloblasts, respectively were used. These results suggested that dental epithelial cells are more closely related to secretion of matrix vesicles than dental mesenchymal cells.

Free Research Field

小児歯科学

URL: 

Published: 2019-03-29  

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