Pathway-oriented profiling of lipid mediators in macrophages

被引:33
作者
Kita, Y
Takahashi, T
Uozumi, N
Nallan, L
Gelb, MH
Shimizu, T
机构
[1] Univ Tokyo, Fac Med, Dept Biochem & Mol Biol, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Washington, Dept Chem & Biochem, Seattle, WA 98195 USA
关键词
eicosanoids; platelet-activating factor; macrophages; lipidomics; pathway analysis; mass spectrometry;
D O I
10.1016/j.bbrc.2005.03.055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages produce various kinds of lipid mediators including eicosanoids and platelet-activating factor. Since they are produced from common precursors, arachidonic acid-containing phospholipids, regulations of metabolic pathways underlie the patterning of lipid mediator production. Here, we report a pathway-oriented profiling strategy of lipid mediators by a newly developed multiplex quantification system. We profiled mouse peritoneal macrophages in different activation states. The analysis of kinetics revealed the differences in the production time course of various lipid mediators, which also differed by the macrophage types. Scatterplot matrix analysis of the inhibitor study revealed correlations of lipid mediator species. The changes of these correlations provided estimates on the effects of lipopolysaccharide priming. We also found a highly linked production of 11-hydroxyeicosatetraenoic acid and prostaglandin E-2, implying the in vivo property of cyclooxygenase-mediated 11-hydroxyeicosatetraenoic acid production. The present approach will serve as a strategy for understanding the regulatory mechanism of lipid mediator production. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:898 / 906
页数:9
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