Division of Advanced Materials and Healthcare Technologies, Centre for Analytical Bioscience, School of Pharmacy, University of Nottingham, Nottingham, UK.
Department of Pharmaceutical Sciences and Pharmaceutics, Faculty of Pharmacy, Applied Science Private University, Amman, Jordan.
Metabolomics. 2020 Feb 29;16(3):33. doi: 10.1007/s11306-020-01656-4.
Macrophages constitute a heterogeneous population of functionally distinct cells involved in several physiological and pathological processes. They display remarkable plasticity by changing their phenotype and function in response to environmental cues representing a spectrum of different functional phenotypes. The so-called M1 and M2 macrophages are often considered as representative of pro- and anti-inflammatory ends of such spectrum. Metabolomics approach is a powerful tool providing important chemical information about the cellular phenotype of living systems, and the changes in their metabolic pathways in response to various perturbations.
This study aimed to characterise M1 and M2 phenotypes in THP-1 macrophages in order to identify characteristic metabolites of each polarisation state.
Herein, untargeted liquid chromatography (LC)-mass spectrometry (MS)-based metabolite profiling was applied to characterise the metabolic profile of M1-like and M2-like THP-1 macrophages.
The results showed that M1 and M2 macrophages have distinct metabolic profiles. Sphingolipid and pyrimidine metabolism was significantly changed in M1 macrophages whereas arginine, proline, alanine, aspartate and glutamate metabolism was significantly altered in M2 macrophages.
This study represents successful application of LC-MS metabolomics approach to characterise M1 and M2 macrophages providing functional readouts that show unique metabolic signature for each phenotype. These data could contribute to a better understanding of M1 and M2 functional properties and could pave the way for developing new therapeutics targeting different immune diseases.
巨噬细胞构成了功能不同的异质性细胞群体,参与多种生理和病理过程。它们通过改变表型和功能来响应环境信号,表现出显著的可塑性,这种环境信号代表了不同功能表型的一系列变化。所谓的 M1 和 M2 巨噬细胞通常被认为是代表这种谱的促炎和抗炎两端。代谢组学方法是一种强大的工具,可提供有关活系统细胞表型的重要化学信息,以及它们的代谢途径在响应各种扰动时的变化。
本研究旨在表征 THP-1 巨噬细胞中的 M1 和 M2 表型,以确定每种极化状态的特征代谢物。
本文应用非靶向液相色谱(LC)-质谱(MS)代谢组学方法来表征 M1 样和 M2 样 THP-1 巨噬细胞的代谢谱。
结果表明,M1 和 M2 巨噬细胞具有不同的代谢谱。M1 巨噬细胞中鞘脂和嘧啶代谢显著改变,而 M2 巨噬细胞中精氨酸、脯氨酸、丙氨酸、天冬氨酸和谷氨酸代谢显著改变。
本研究成功应用 LC-MS 代谢组学方法来表征 M1 和 M2 巨噬细胞,提供了功能读数,显示每种表型具有独特的代谢特征。这些数据有助于更好地理解 M1 和 M2 的功能特性,并为开发针对不同免疫疾病的新型治疗方法铺平道路。