mTORC1型
免疫系统
糖酵解
P70-S6激酶1
锌
化学
激酶
磷酸化
细胞生物学
生物
癌症研究
信号转导
生物化学
免疫学
新陈代谢
PI3K/AKT/mTOR通路
有机化学
作者
Bonah Kim,Hee Young Kim,Bo Ruem Yoon,Jina Yeo,Ji In Jung,Kyung‐Sang Yu,Hyeon Chang Kim,Su‐Jin Yoo,Jin Kyun Park,Seong Wook Kang,Won‐Woo Lee
出处
期刊:Science Signaling
[American Association for the Advancement of Science]
日期:2022-01-11
卷期号:15 (716): eabi7400-eabi7400
被引量:47
标识
DOI:10.1126/scisignal.abi7400
摘要
The essential micronutrient zinc regulates immune responses by affecting signaling pathways. In activated monocytes and macrophages, signaling networks mediate the metabolic reprogramming that meets the demands of participation in immune responses. Here, we demonstrated that cytoplasmic, bioavailable zinc was essential for promoting IL-1β production in activated human monocytes and macrophages downstream of glycolysis induced by the kinase-containing multiprotein complex mTORC1. The concentration of cytoplasmic zinc was determined by that of extracellular zinc, which was brought into cells through the zinc-specific importer Zip8. The abundance of Zip8 was increased in monocytes from patients with rheumatoid arthritis (RA), as well as in LPS-stimulated monocytes and macrophages from healthy individuals. The mTORC1-mediated phosphorylation of S6 kinase (S6K) was enhanced by zinc-mediated inhibition of PP2A, a phosphatase that targets S6K. As a result, IL-1β production was increased due to the activation of mTORC1-induced glycolysis. In monocytes of patients with RA, the expression of Zip8 and the zinc-inducible metallothionein isoform MT2A and the phosphorylation of S6K were enhanced compared with those of healthy controls. Furthermore, Zip8 expression correlated with more severe RA clinical parameters, suggesting that Zip8-mediated zinc influx is related to inflammatory conditions. These results provide insight into the role of cytoplasmic, bioavailable zinc in the metabolic reprogramming of human monocytes and macrophages in inflammatory responses.
科研通智能强力驱动
Strongly Powered by AbleSci AI