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2016 Fiscal Year Final Research Report

Investigation on inhibitory mechanism of soluble ST2 protein (secreted IL-33 receptor) against LPS signal

Research Project

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Project/Area Number 26460376
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field General medical chemistry
Research InstitutionJichi Medical University

Principal Investigator

Yanagisawa Ken  自治医科大学, 医学部, 教授 (50182366)

Project Period (FY) 2014-04-01 – 2017-03-31
KeywordsST2 / LPS / シグナル伝達 / 細胞がん化
Outline of Final Research Achievements

We investigated the mechanism of inhibitory effect of soluble ST2 protein, which is the extracellular domain of IL-33 receptor (ST2L protein), against the LPS signal transduction. ST2 protein did not inhibit the binding of LPS with LPS receptor. Each component of LPS receptor complex, TLR 4, CD14 and MD2, did not show the binding with ST2 protein, and each combination of two components of above also failed to bind with ST2, which suggests higher structure of LPS receptor complex is required for the binding with ST2.
Furthermore, We found novel proteins such as IFITM3 which bind with ST2L protein, and IL-33 is indispensable for the cellular transformation by Ras independent of ST2 protein, and IL-33 promotes the translation of cyclin D.

Free Research Field

生化学

URL: 

Published: 2018-03-22  

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