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2016 Fiscal Year Final Research Report

Effect of transcriptional factor Alx3 during osteoblast differentiation and bone development

Research Project

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Project/Area Number 26861684
Research Category

Grant-in-Aid for Young Scientists (B)

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

Principal Investigator

Matsumoto Takashi  昭和大学, 歯学部, 助教 (00635039)

Project Period (FY) 2014-04-01 – 2017-03-31
KeywordsAlx3 / BMP
Outline of Final Research Achievements

In this study, we demonstrated the mechanisms of Alx3 gene expression and function during osteoblast differentiation induced by BMP-2. In C2C12 cells, BMP-2 induced increase of Alx3 gene expression in both time- and dose-dependent manners through the Smad signaling pathway. In addition, silencing of Alx3 br siRNA inhibited osteoblast differentiation induced by BMP-2, as showed by the expressions of Alkaline phosphatase (ALP), Osteocaltin, and Osterix, while overexpression of Alx3 enhanced osteoblast differentiation induced by BMP-2. According to Alx3 CHIP assay, osteoblastic marker gene ALP is the target gene of Alx3 transcriptional factor. These results indicate that Alx3 is a positive regurator of osteoblast differentiation induced by BMP-2. However, we found that effect of osteoblast diffarentiation by Alx3 is not enough and therefore Alx3 applied bone development is dificult.

Free Research Field

歯学

URL: 

Published: 2018-03-22  

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