Kita Yoshihiro, Takahashi Toshie, Uozumi Naonori, Nallan Laxman, Gelb Michael H, Shimizu Takao
Department of Biochemistry and Molecular Biology, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Biochem Biophys Res Commun. 2005 May 13;330(3):898-906. doi: 10.1016/j.bbrc.2005.03.055.
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 E2, 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.
巨噬细胞产生多种脂质介质,包括类花生酸和血小板活化因子。由于它们由共同的前体——含花生四烯酸的磷脂产生,代谢途径的调控是脂质介质产生模式的基础。在此,我们报告一种通过新开发的多重定量系统对脂质介质进行面向途径的分析策略。我们对处于不同激活状态的小鼠腹腔巨噬细胞进行了分析。动力学分析揭示了各种脂质介质产生时间进程的差异,这些差异也因巨噬细胞类型而异。抑制剂研究的散点图矩阵分析揭示了脂质介质种类之间的相关性。这些相关性的变化提供了关于脂多糖预处理效果的估计。我们还发现11-羟基二十碳四烯酸和前列腺素E2的产生高度相关,这意味着环氧化酶介导的11-羟基二十碳四烯酸产生具有体内特性。本方法将作为一种理解脂质介质产生调控机制的策略。