Key Points
Berberine induces aerobic glycolysis and expression of GLUT1/HK2 in BMDMs.
Berberine priming increases cytokine secretion by BMDMs triggered with LPS.
Berberine alleviates Salmonella typhimurium enteritis and endotoxic shock.
Abstract
Classical activation of macrophage and monocyte differentiation induced by β-glucan is accompanied with metabolic change in glucose. However, the role of the metabolic rewiring in monocyte/macrophage activation remains elusive. In this study, we show that berberine induces aerobic glycolysis by blocking the tricarboxylic acid cycle and modulates cytokine responses in bone marrow–derived macrophages (BMDMs) from mice and human PBMC. 13-Methyberberine had activities on glucose metabolism and BMDM activation similar to those of berberine, whereas other tested derivatives lost both activities. Glucose transporter (GLUT)1 expression and total cellular hexokinase activity increased gradually in BMDMs in the presence of berberine. In the contrast, LPS upregulated GLUT1 and 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3) levels in 6 h. Extracellular glucose levels and replacing glucose with galactose in culture medium affected the cytokine secretion of BMDMs. Berberine alleviated enteritis of Salmonella typhimurium infection and protected mice against endotoxic shock. In mice i.p. injected with LPS, the increase of serum TNF-α and the drop of blood glucose were attenuated by berberine treatment. These data together demonstrated that macrophage activation was closely related with glucose metabolism.
Footnotes
This work was supported by Startup Foundation of Zhengzhou University Grant 32210549 and by Science and Technology Department, Henan Province Grant 32240073.
The online version of this article contains supplemental material.
Abbreviations used in this article:
- BCG
- bacillus Calmette–Guérin
- BMDM
- bone marrow–derived macrophage
- GLUT
- glucose transporter
- HK
- hexokinase
- LDH
- lactate dehydrogenase
- MeOH
- methanol
- PFKFB3
- 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3
- PKM2
- pyruvate kinase M2
- qPCR
- quantitative PCR
- ROS
- reactive oxygen species
- SMP
- submitochondrial particle
- TCA
- tricarboxylic acid
- Received July 19, 2021.
- Accepted February 28, 2022.
- Copyright © 2022 by The American Association of Immunologists, Inc.
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