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2014 Fiscal Year Final Research Report

Analysis of a novel transcriptional repressor involved in energy metabolism and application for metabolic liver diseases

Research Project

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Project/Area Number 24659360
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Gastroenterology
Research InstitutionUniversity of Fukui

Principal Investigator

NEMOTO Tomoyuki  福井大学, 医学部, 助教 (20397277)

Co-Investigator(Renkei-kenkyūsha) YOKOTA Yoshifumi  福井大学, 医学部, 教授 (50222386)
Project Period (FY) 2012-04-01 – 2015-03-31
Keywords糖代謝 / インスリンシグナル
Outline of Final Research Achievements

A dominant-negative transcriptional repressor, Id2 has been shown to regulate cell differentiation and proliferation. Id2 knockout mice have lean phenotype. Id2 deficiency conferred resistance to obesity and fatty liver development in a mouse model. Id2 knockout mice showed increased glucose tolerance and insulin sensitivity. Id2 was induced by insulin and mediated by phosphatidylinositol-3 kinase pathway. An increase of Id2 expression by insulin may be indispensable for adipocyte differentiation. Modulation of Id2 expression is thought to be a potential therapeutic target for fatty liver, metabolic syndrome, and furthermore, lifestyle-related diseases.

Free Research Field

消化器内科

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Published: 2016-06-03  

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