Curi Rui, de Siqueira Mendes Renata, de Campos Crispin Luiz Aurélio, Norata Giuseppe Danilo, Sampaio Sandra Coccuzzo, Newsholme Philip
Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, 1524, SP 05508-900, Brazil.
Laboratory of Pathophysiology, Butantan Institute, Av. Vital Brazil, 1500, SP 05503-900, São Paulo, Brazil.
Clin Sci (Lond). 2017 Jun 15;131(12):1329-1342. doi: 10.1042/CS20170220.
In 1986 and 1987, Philip Newsholme et al. reported macrophages utilize glutamine, as well as glucose, at high rates. These authors measured key enzyme activities and consumption and production levels of metabolites in incubated or cultured macrophages isolated from the mouse or rat intraperitoneal cavity. Metabolic pathways essential for macrophage function were then determined. Macrophages utilize glucose to generate (i) ATP in the pathways of glycolysis and mitochondrial oxidative phosphorylation, (ii) glycerol 3-phosphate for the synthesis of phospholipids and triacylglycerols, (iii) NADPH for the production of reactive oxygen species (ROS) and (iv) ribose for the synthesis of RNA and subsequently production and secretion of protein mediators (e.g. cytokines). Glutamine plays an essential role in macrophage metabolism and function, as it is required for energy production but also provides nitrogen for synthesis of purines, pyrimidines and thus RNA. Macrophages also utilize fatty acids for both energy production in the mitochondria and lipid synthesis essential to plasma membrane turnover and lipid meditator production. Recent studies utilizing metabolomic approaches, transcriptional and metabolite tracking technologies have detailed mitochondrial release of tricarboxylic acid (TCA) intermediates (e.g. citrate and succinate) to the cytosol, which then regulate pro-inflammatory responses. Macrophages can reprogramme their metabolism and function according to environmental conditions and stimuli in order to polarize phenotype so generating pro- or anti-inflammatory cells. Changes in macrophage metabolism result in modified function/phenotype and vice versa. The plasticity of macrophage metabolism allows the cell to quickly respond to changes in environmental conditions such as those induced by hormones and/or inflammation. A past and present overview of macrophage metabolism and impact of endocrine regulation and the relevance to human disease are described in this review.
1986年和1987年,菲利普·纽肖尔姆等人报告称,巨噬细胞会大量利用谷氨酰胺以及葡萄糖。这些作者测量了从小鼠或大鼠腹腔分离出的培养巨噬细胞中关键酶的活性以及代谢物的消耗和生成水平。随后确定了巨噬细胞功能所必需的代谢途径。巨噬细胞利用葡萄糖来生成:(i) 糖酵解和线粒体氧化磷酸化途径中的ATP;(ii) 用于合成磷脂和三酰甘油的3-磷酸甘油;(iii) 用于产生活性氧(ROS)的NADPH;(iv) 用于合成RNA以及随后生成和分泌蛋白质介质(如细胞因子)的核糖。谷氨酰胺在巨噬细胞代谢和功能中起着至关重要的作用,因为它不仅是能量生成所必需的,还为嘌呤、嘧啶以及RNA的合成提供氮。巨噬细胞还利用脂肪酸进行线粒体中的能量生成以及对质膜更新和脂质介质生成至关重要的脂质合成。最近利用代谢组学方法、转录和代谢物追踪技术的研究详细阐述了三羧酸(TCA)中间体(如柠檬酸和琥珀酸)从线粒体释放到细胞质中,进而调节促炎反应。巨噬细胞可以根据环境条件和刺激重新编程其代谢和功能,以使表型极化,从而产生促炎或抗炎细胞。巨噬细胞代谢的变化会导致功能/表型的改变,反之亦然。巨噬细胞代谢的可塑性使细胞能够快速响应环境条件的变化,如激素和/或炎症引起的变化。本综述描述了巨噬细胞代谢的过去和现在概况、内分泌调节的影响以及与人类疾病的相关性。