Macrophage Immunometabolism: Where Are We (Going)?

被引:786
作者
Van den Bossche, Jan [1 ]
O'Neill, Luke A. [2 ]
Menon, Deepthi [2 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Med Biochem, Expt Vasc Biol, Amsterdam, Netherlands
[2] Trinity Coll Dublin, Trinity Biomed Sci Inst, Sch Biochem & Immunol, Dublin, Ireland
关键词
FATTY-ACID OXIDATION; NLRP3 INFLAMMASOME ACTIVATION; SYNTHASE ARGINASE BALANCE; ATP-CITRATE LYASE; SUCCINATE-DEHYDROGENASE; PROMOTES NLRP3; PYRUVATE-DEHYDROGENASE; METABOLIC-CONTROL; MESSENGER-RNA; KREBS CYCLE;
D O I
10.1016/j.it.2017.03.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A growing number of findings highlight the crucial role of metabolic reprogramming in macrophage activation. Metabolic pathways are closely interconnected and recent literature demonstrates the need for glucose metabolism in anti-inflammatory as well as inflammatory macrophages. Moreover, fatty acid oxidation (FAO) not only supports anti-inflammatory responses as described formerly but also drives inflammasome activation in inflammatory macrophages. Hence, defining glycolysis as proinflammatory and FAO as anti-inflammatory may be an oversimplification. Here we review how the rapid growth of the immunometabolism field has improved our understanding of macrophage activation and at the same time has led to an increase in the appearance of contradictory observations. To conclude we discuss current challenges in immunometabolism and present crucial areas for future research.
引用
收藏
页码:395 / 406
页数:12
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