小胶质细胞
生物
炎症
重编程
细胞生物学
免疫系统
中枢神经系统
代谢途径
氧化磷酸化
神经科学
表型
糖酵解
新陈代谢
免疫学
细胞
生物化学
基因
作者
Sheng Yang,Chuan Qin,Zi-Wei Hu,Luo Zhou,Hai-Han Yu,Man Chen,Dale B. Bosco,Wei Wang,Long‐Jun Wu,Dai‐Shi Tian
标识
DOI:10.1016/j.nbd.2021.105290
摘要
In response to various types of environmental and cellular stress, microglia rapidly activate and exhibit either pro- or anti-inflammatory phenotypes to maintain tissue homeostasis. Activation of microglia can result in changes in morphology, phagocytosis capacity, and secretion of cytokines. Furthermore, microglial activation also induces changes to cellular energy demand, which is dependent on the metabolism of various metabolic substrates including glucose, fatty acids, and amino acids. Accumulating evidence demonstrates metabolic reprogramming acts as a key driver of microglial immune response. For instance, microglia in pro-inflammatory states preferentially use glycolysis for energy production, whereas, cells in anti-inflammatory states are mainly powered by oxidative phosphorylation and fatty acid oxidation. In this review, we summarize recent findings regarding microglial metabolic pathways under physiological and pathological circumtances. We will then discuss how metabolic reprogramming can orchestrate microglial response to a variety of central nervous system pathologies. Finally, we highlight how manipulating metabolic pathways can reprogram microglia towards beneficial functions, and illustrate the therapeutic potential for inflammation-related neurological diseases.
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