Department of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Department of Neurology, Mayo Clinic, Rochester, MN 55905, United States of America.
Neurobiol Dis. 2021 May;152:105290. doi: 10.1016/j.nbd.2021.105290. Epub 2021 Feb 5.
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.
在应对各种类型的环境和细胞应激时,小胶质细胞会迅速激活,并表现出促炎或抗炎表型,以维持组织内稳态。小胶质细胞的激活可导致形态、吞噬能力和细胞因子分泌的变化。此外,小胶质细胞的激活还会引起细胞能量需求的变化,这依赖于各种代谢底物的代谢,包括葡萄糖、脂肪酸和氨基酸。越来越多的证据表明,代谢重编程是小胶质细胞免疫反应的关键驱动因素。例如,在促炎状态下的小胶质细胞优先利用糖酵解产生能量,而在抗炎状态下的细胞主要由氧化磷酸化和脂肪酸氧化供能。在这篇综述中,我们总结了生理和病理条件下小胶质细胞代谢途径的最新发现。然后,我们将讨论代谢重编程如何协调小胶质细胞对各种中枢神经系统疾病的反应。最后,我们强调了如何通过操纵代谢途径将小胶质细胞重编程为有益的功能,并说明了与炎症相关的神经疾病的治疗潜力。