受体
炎症
肺泡巨噬细胞
清道夫受体
先天免疫系统
甘露糖
肿瘤坏死因子α
生物
6-磷酸甘露糖
传出细胞增多
吞噬作用
作者
Maria Embgenbroich,Hendrik J. P. van der Zande,Leonie Hussaarts,Jonas Schulte-Schrepping,Leonard R. Pelgrom,Noemí García-Tardón,Laura Schlautmann,Isabel Stoetzel,Kristian Händler,Joost M. Lambooij,Anna Zawistowska-Deniziak,Lisa R. Hoving,Karin de Ruiter,Marjolein A. Wijngaarden,Hanno Pijl,Ko Willems van Dijk,Bart Everts,Vanessa van Harmelen,Maria Yazdanbakhsh,Joachim L. Schultze,Bruno Guigas,Sven Burgdorf
标识
DOI:10.1073/pnas.2103304118
摘要
Proinflammatory activation of macrophages in metabolic tissues is critically important in the induction of obesity-induced metaflammation. Here, we demonstrate that the soluble mannose receptor (sMR) plays a direct functional role in both macrophage activation and metaflammation. We show that sMR binds CD45 on macrophages and inhibits its phosphatase activity, leading to an Src/Akt/NF-κB-mediated cellular reprogramming toward an inflammatory phenotype both in vitro and in vivo. Remarkably, increased serum sMR levels were observed in obese mice and humans and directly correlated with body weight. Importantly, enhanced sMR levels increase serum proinflammatory cytokines, activate tissue macrophages, and promote insulin resistance. Altogether, our results reveal sMR as regulator of proinflammatory macrophage activation, which could constitute a therapeutic target for metaflammation and other hyperinflammatory diseases.
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