Centre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Clayton, VIC, 3168, Australia.
Department of Molecular and Translational Sciences, Monash University, Clayton, VIC, 3168, Australia.
Nat Commun. 2020 Jul 30;11(1):3816. doi: 10.1038/s41467-020-17669-5.
Detection of microbial components such as lipopolysaccharide (LPS) by Toll-like receptor 4 (TLR4) on macrophages induces a robust pro-inflammatory response that is dependent on metabolic reprogramming. These innate metabolic changes have been compared to aerobic glycolysis in tumour cells. However, the mechanisms by which TLR4 activation leads to mitochondrial and glycolytic reprogramming are unknown. Here we show that TLR4 activation induces a signalling cascade recruiting TRAF6 and TBK-1, while TBK-1 phosphorylates STAT3 on S727. Using a genetically engineered mouse model incapable of undergoing STAT3 Ser727 phosphorylation, we show ex vivo and in vivo that STAT3 Ser727 phosphorylation is critical for LPS-induced glycolytic reprogramming, production of the central immune response metabolite succinate and inflammatory cytokine production in a model of LPS-induced inflammation. Our study identifies non-canonical STAT3 activation as the crucial signalling intermediary for TLR4-induced glycolysis, macrophage metabolic reprogramming and inflammation.
巨噬细胞上的 Toll 样受体 4(TLR4)检测微生物成分,如脂多糖(LPS),会引发依赖于代谢重编程的强烈促炎反应。这些先天代谢变化与肿瘤细胞中的有氧糖酵解相媲美。然而,TLR4 激活导致线粒体和糖酵解重编程的机制尚不清楚。在这里,我们表明 TLR4 激活诱导了一个信号级联反应,招募 TRAF6 和 TBK-1,而 TBK-1 磷酸化 STAT3 上的 S727。使用一种不能进行 STAT3 Ser727 磷酸化的基因工程小鼠模型,我们在体外和体内表明,STAT3 Ser727 磷酸化对于 LPS 诱导的糖酵解重编程、中央免疫反应代谢物琥珀酸的产生以及 LPS 诱导的炎症模型中炎症细胞因子的产生至关重要。我们的研究确定了非典型 STAT3 激活是 TLR4 诱导的糖酵解、巨噬细胞代谢重编程和炎症的关键信号中介。
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