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2017 Fiscal Year Final Research Report

Molecular mechanisms of cell death in macrophages and foam cells

Research Project

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Project/Area Number 15K08429
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Experimental pathology
Research InstitutionUniversity of the Ryukyus

Principal Investigator

TAKAESU Giichi  琉球大学, 熱帯生物圏研究センター, 准教授 (60403995)

Project Period (FY) 2015-04-01 – 2018-03-31
Keywordsマクロファージ / 細胞死 / 炎症
Outline of Final Research Achievements

Macrophages are the major immune cells in the atherosclerotic lesions and play important roles in disease progression. Macrophages uptake oxidized low density lipoproteins (oxLDL) and differentiate into foam cells. Foam cells eventually undergo apoptosis or necroptosis. The former is thought to be protective, but the latter is thought to be detrimental. To develop new therapeutics for atherosclerosis, it is necessary to understand the molecular mechanisms of programmed cell death in macrophages and foam cells. In this study, I have investigated the roles of TAB2 and its close homolog TAB3 in macrophages and foam cells. Tab2/3-deficient foam cells underwent necrosis. In addition, TAB2, but not TAB3, was essential for suppression of TNF-induced necroptosis, which was responsible for the inflammasome activation in LPS-primed Tab2-deficient macrophages. These findings will help to develop novel strategies to treat atherosclerosis and other inflammatory diseases.

Free Research Field

自然免疫

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Published: 2019-03-29  

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