Department of Molecular Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236 Lodz, Poland.
Unité de Recherche MolSys, Faculté des sciences, Université de Liège, 4000 Liège, Belgium.
Int J Mol Sci. 2020 Sep 18;21(18):6843. doi: 10.3390/ijms21186843.
Biological organisms are constantly exposed to an immense repertoire of molecules that cover environmental or food-derived molecules and drugs, triggering a continuous flow of stimuli-dependent adaptations. The diversity of these chemicals as well as their concentrations contribute to the multiplicity of induced effects, including activation, stimulation, or inhibition of physiological processes and toxicity. Metabolism, as the foremost phenotype and manifestation of life, has proven to be immensely sensitive and highly adaptive to chemical stimuli. Therefore, studying the effect of endo- or xenobiotics over cellular metabolism delivers valuable knowledge to apprehend potential cellular activity of individual molecules and evaluate their acute or chronic benefits and toxicity. The development of modern metabolomics technologies such as mass spectrometry or nuclear magnetic resonance spectroscopy now offers unprecedented solutions for the rapid and efficient determination of metabolic profiles of cells and more complex biological systems. Combined with the availability of well-established cell culture techniques, these analytical methods appear perfectly suited to determine the biological activity and estimate the positive and negative effects of chemicals in a variety of cell types and models, even at hardly detectable concentrations. Metabolic phenotypes can be estimated from studying intracellular metabolites at homeostasis in vivo, while in vitro cell cultures provide additional access to metabolites exchanged with growth media. This article discusses analytical solutions available for metabolic phenotyping of cell culture metabolism as well as the general metabolomics workflow suitable for testing the biological activity of molecular compounds. We emphasize how metabolic profiling of cell supernatants and intracellular extracts can deliver valuable and complementary insights for evaluating the effects of xenobiotics on cellular metabolism. We note that the concepts and methods discussed primarily for xenobiotics exposure are widely applicable to drug testing in general, including endobiotics that cover active metabolites, nutrients, peptides and proteins, cytokines, hormones, vitamins, etc.
生物机体不断暴露于大量的分子中,这些分子包括环境或食物来源的分子以及药物,从而引发了一系列依赖于刺激的适应性变化。这些化学物质的多样性及其浓度导致了多种诱导效应,包括对生理过程的激活、刺激或抑制以及毒性。代谢作为生命的首要表型和表现形式,已经被证明对化学刺激具有极高的敏感性和适应性。因此,研究内源性或外源性化学物质对细胞代谢的影响,可以为理解单个分子的潜在细胞活性提供有价值的知识,并评估其急性或慢性益处和毒性。现代代谢组学技术,如质谱或核磁共振波谱学的发展,为快速高效地确定细胞和更复杂的生物系统的代谢谱提供了前所未有的解决方案。结合成熟的细胞培养技术,这些分析方法非常适合确定各种细胞类型和模型中化学物质的生物活性,并评估其积极和消极影响,即使在难以检测到的浓度下也是如此。可以通过研究体内细胞内代谢物的内稳态来估计代谢表型,而体外细胞培养则提供了与生长培养基交换的代谢物的额外途径。本文讨论了用于细胞培养代谢代谢表型分析的分析解决方案,以及适用于测试分子化合物生物活性的一般代谢组学工作流程。我们强调了细胞上清液和细胞内提取物的代谢谱分析如何为评估外源性化学物质对细胞代谢的影响提供有价值的互补见解。我们注意到,本文讨论的主要用于外源性化学物质暴露的概念和方法广泛适用于一般的药物测试,包括涵盖活性代谢物、营养物质、肽和蛋白质、细胞因子、激素、维生素等的内源性化学物质。