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2014 Fiscal Year Final Research Report

Biological functions and mechanisms of unliganded VDR on bone and calcium metabolism.

Research Project

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Project/Area Number 24614004
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Integrated Nutrition Science
Research InstitutionThe University of Tokyo

Principal Investigator

YAMAMOTO Yoko  東京大学, 医学部附属病院, 助教 (30376644)

Project Period (FY) 2012-04-01 – 2015-03-31
KeywordsビタミンD / ビタミンD受容体 / カルシウム代謝 / 骨代謝
Outline of Final Research Achievements

Vitamin D is a primary regulator in many biological phenomena such as calcium homeostasis and bone formation. Such actions are thought to be mediated through transcriptional controls by the vitamin D receptor (VDR). Ligand-induced function of VDR have been well established, however, the physiological impact of unliganded VDR still remains unclear. Here we report that VDR helix 12 deletion (ΔAF2) mutant mice fed with high calcium diet exhibited impaired bone formation unlike VDRKO mice. Trabeculae in VDRΔAF2 mice were filled with fibroblast-like cells instead of bone marrow. Microarray and real-time RT-PCR analyses of kidney in VDRKO and VDRΔAF2 mice reveal distinct gene expression profiles. Six putative target genes regulated by unliganded VDR and responsible for impaired bone formation were identified.

Free Research Field

分子生物学

URL: 

Published: 2016-06-03  

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