School of Chemistry and Biochemistry, College of Sciences. Georgia Institute of Technology, IBB, Parker H. Petit Institute for Bioengineering and Biosciences, Atlanta, GA 30332, USA.
Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Prostaglandins Other Lipid Mediat. 2024 Oct;174:106839. doi: 10.1016/j.prostaglandins.2024.106839. Epub 2024 Apr 26.
Immune responses during inflammation involve complex, well-coordinated lipid signaling pathways. Eicosanoids are a class of lipid signaling molecules derived from polyunsaturated fatty acids such as arachidonic acid and constitute a major network that controls inflammation and its subsequent resolution. Arachidonic acid is metabolized by enzymes in three different pathways to form a variety of lipid metabolites that can be either pro- or anti-inflammatory. Therefore, an understanding of the time-dependent gene expression, lipid metabolite profiles and cytokine profiles during the initial inflammatory response is necessary, as it will allow for the design of time-dependent therapeutics. Herein, we investigate the multi-level regulation of this process. After stimulating RAW 264.7 cells, a mouse-derived macrophage cell line commonly used to examine inflammatory responses, we examine the gene expression of 44 relevant lipid metabolizing enzymes from the different eicosanoid synthesizing classes. We also measure the formation of lipid metabolites and production of cytokines at selected time points. Results reveal a dynamic relationship between the time-course of inflammation dependent gene expression of the three eicosanoid synthesizing enzymes.
在炎症过程中,免疫反应涉及复杂的、协调良好的脂质信号通路。类二十烷酸是一类源自多不饱和脂肪酸(如花生四烯酸)的脂质信号分子,构成了控制炎症及其随后消退的主要网络。花生四烯酸可被三种不同途径的酶代谢,形成多种具有促炎或抗炎作用的脂质代谢物。因此,有必要了解初始炎症反应过程中基因表达、脂质代谢物谱和细胞因子谱的时变特征,这将有助于设计时变治疗方法。在此,我们研究了这一过程的多层次调节。在刺激 RAW 264.7 细胞(一种常用于研究炎症反应的鼠源性巨噬细胞系)后,我们检查了 44 种不同类二十烷酸合成酶相关的脂质代谢酶的基因表达。我们还在选定的时间点测量脂质代谢物的形成和细胞因子的产生。结果揭示了三种类二十烷酸合成酶炎症相关基因表达的时程与炎症之间的动态关系。