| Literature DB >> 33556540 |
Sheng Yang1, Chuan Qin1, Zi-Wei Hu1, Luo-Qi Zhou1, Hai-Han Yu1, Man Chen1, Dale B Bosco2, Wei Wang1, Long-Jun Wu3, Dai-Shi Tian4.
Abstract
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.Entities:
Keywords: Glycolysis; Inflammation; Metabolism; Microglia; Oxidative phosphorylation; Reprogramming
Mesh:
Year: 2021 PMID: 33556540 DOI: 10.1016/j.nbd.2021.105290
Source DB: PubMed Journal: Neurobiol Dis ISSN: 0969-9961 Impact factor: 5.996