1Transplantation Biology Research Division, State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Int Rev Immunol. 2015 Jan;34(1):82-100. doi: 10.3109/08830185.2014.969421. Epub 2014 Oct 23.
Macrophages are a functionally heterogeneous cell population that is mainly shaped by a variety of microenvironmental stimuli. Interferon γ (IFN-γ), interleukin-1β (IL-1β), and lipopolysaccharide (LPS) induce a classical activation of macrophages (M1), whereas IL-4 and IL-13 induce an alternative activation program in macrophages (M2). Reprogramming of intracellular metabolisms is required for the proper polarization and functions of activated macrophages. Similar to the Warburg effect observed in tumor cells, M1 macrophages increase glucose consumption and lactate release and decreased oxygen consumption rate. In comparison, M2 macrophages mainly employ oxidative glucose metabolism pathways. In addition, fatty acids, vitamins, and iron metabolisms are also related to macrophage polarization. However, detailed metabolic pathways involved in macrophages have remained elusive. Understanding the bidirectional interactions between cellular metabolism and macrophage functions in physiological and pathological situations and the regulatory pathways involved may offer novel therapies for macrophage-associated diseases.
巨噬细胞是一种功能异质性的细胞群体,主要由各种微环境刺激塑造。干扰素 γ(IFN-γ)、白细胞介素 1β(IL-1β)和脂多糖(LPS)诱导巨噬细胞的经典激活(M1),而白细胞介素 4 和白细胞介素 13 则在巨噬细胞中诱导替代激活程序(M2)。细胞内代谢的重新编程是激活的巨噬细胞正确极化和功能所必需的。类似于肿瘤细胞中观察到的瓦博格效应,M1 巨噬细胞增加葡萄糖消耗和乳酸释放,降低耗氧率。相比之下,M2 巨噬细胞主要采用氧化葡萄糖代谢途径。此外,脂肪酸、维生素和铁代谢也与巨噬细胞极化有关。然而,巨噬细胞中涉及的详细代谢途径仍不清楚。了解生理和病理情况下细胞代谢与巨噬细胞功能之间的双向相互作用以及涉及的调节途径,可能为与巨噬细胞相关的疾病提供新的治疗方法。