Pomeyie Karen, Abrokwah Francis, Boison Daniel, Amoani Benjamin, Kyei Foster, Adinortey Cynthia A, Barnie Prince Amoah
Department of Microbiology and Immunology, School of Medical Sciences, College of Health and Allied Sciences, University of Cape Coast, Cape Coast, Ghana.
Department of Biochemistry, School of Biological Sciences University of Cape Coast, Cape Coast, Ghana.
Biomed Pharmacother. 2025 Jul;188:118142. doi: 10.1016/j.biopha.2025.118142. Epub 2025 May 15.
Macrophages are innate immune cells which are involved in triggering inflammation. Growing evidence shows that, macrophages respond to intracellular and extracellular cues which makes them adopt either anti-inflammatory or pro-inflammatory functions and phenotypes. Immunometabolism has been identified as one of the prominent factors which contributes massively towards the cessation and the development of inflammation as an immune response to infections and autoimmune diseases. However, when inflammation is poorly regulated, it leads to dire consequences. This illustrates that, understanding the role of immunometabolism in the regulation of inflammation, is paramount. In view of this, the review investigated the role of metabolic pathways such as: glycolysis, tricarboxylic acid cycle, pentose phosphate pathway, fatty acid oxidation, amino acid metabolism in macrophage reprogramming. The role of the intermediates and enzymes associated with these metabolic pathways in the regulation of, macrophage reprogramming and polarisation or activation was also reviewed. It was unveiled that, manipulating metabolic intermediates and enzymes could impact cellular immunometabolism. This eventually influences macrophage reprogramming and thus influences the generation of either a pro-inflammatory or anti-inflammatory response.
巨噬细胞是参与引发炎症的固有免疫细胞。越来越多的证据表明,巨噬细胞会对细胞内和细胞外信号作出反应,这使得它们呈现出抗炎或促炎功能及表型。免疫代谢已被确认为对炎症的停止和发展有重大贡献的突出因素之一,炎症是对感染和自身免疫性疾病的免疫反应。然而,当炎症调节不佳时,会导致严重后果。这表明,了解免疫代谢在炎症调节中的作用至关重要。有鉴于此,本综述研究了糖酵解、三羧酸循环、磷酸戊糖途径、脂肪酸氧化、氨基酸代谢等代谢途径在巨噬细胞重编程中的作用。还综述了与这些代谢途径相关的中间产物和酶在巨噬细胞重编程、极化或激活调节中的作用。研究发现,操纵代谢中间产物和酶会影响细胞免疫代谢。这最终会影响巨噬细胞重编程,从而影响促炎或抗炎反应的产生。