小胶质细胞
神经炎症
重编程
免疫系统
生物
神经科学
阿尔茨海默病
神经胶质
细胞生物学
中枢神经系统
免疫学
炎症
疾病
细胞
医学
内科学
生物化学
作者
Hongli Chen,Zichen Guo,Yaxuan Sun,Xueling Dai
标识
DOI:10.1016/j.neuint.2023.105614
摘要
Alzheimer's disease (AD) is an age-related neurodegenerative disorder (NDD). In the central nervous system (CNS), immune cells like microglia could reprogram intracellular metabolism to alter or exert cellular immune functions in response to environmental stimuli. In AD, microglia could be activated and differentiated into pro-inflammatory or anti-inflammatory phenotypes, and these differences in cellular phenotypes resulted in variance in cellular energy metabolism. Considering the enormous energy requirement of microglia for immune functions, the changes in mitochondria-centered energy metabolism and substrates of microglia are crucial for the cellular regulation of immune responses. Here we reviewed the mechanisms of microglial metabolic reprogramming by analyzing their flexible metabolic patterns and changes that occurred in their metabolism during the development of AD. Further, we summarized the role of drugs in modulating immunometabolic reprogramming to prevent neuroinflammation, which may shed light on a new research direction for AD treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI