炎症体
先天免疫系统
代谢控制分析
代谢途径
生物
细胞生物学
信号转导
免疫系统
炎症
免疫学
酶
生物化学
糖尿病
内分泌学
作者
Antoni Olona,Stuart Leishman,Paras Anand
标识
DOI:10.1016/j.it.2022.10.003
摘要
Macrophages undergo profound metabolic reprogramming upon sensing infectious and sterile stimuli. This metabolic shift supports and regulates essential innate immune functions, including activation of the NLRP3 inflammasome. Within distinct metabolic networks, key enzymes play pivotal roles to control flux restraining detrimental inflammasome signaling. However, depending on the metabolic cues, specific enzymes and metabolites result in inflammasome activation outcomes which contrast other metabolic steps in the pathway. We posit that understanding which metabolic steps commit to discrete inflammasome fates will broaden our understanding of metabolic checkpoints to maintain homeostasis and offer better therapeutic options in human disease.
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