巨噬细胞移动抑制因子
炎症体
炎症
细胞生物学
细胞因子
免疫系统
转录因子
巨噬细胞
肿瘤坏死因子α
化学
免疫学
生物
生物化学
基因
体外
作者
Tali Lang,Jacinta P. W. Lee,Kirstin Elgass,Anita A. Pinar,Michelle D. Tate,Elizabeth H. Aitken,Huapeng Fan,Sarah J. Creed,Nadia S. Deen,Daouda A. K. Traoré,Ivo Müeller,Danielle I. Stanisic,Francesca Baiwog,Colin E. Skene,Matthew C. J. Wilce,Ashley Mansell,Eric F. Morand,James Harris
标识
DOI:10.1038/s41467-018-04581-2
摘要
Macrophage migration inhibitory factor (MIF) exerts multiple effects on immune cells, as well as having functions outside the immune system. MIF can promote inflammation through the induction of other cytokines, including TNF, IL-6, and IL-1 family cytokines. Here, we show that inhibition of MIF regulates the release of IL-1α, IL-1β, and IL-18, not by affecting transcription or translation of these cytokines, but via activation of the NLRP3 inflammasome. MIF is required for the interaction between NLRP3 and the intermediate filament protein vimentin, which is critical for NLRP3 activation. Further, we demonstrate that MIF interacts with NLRP3, indicating a role for MIF in inflammasome activation independent of its role as a cytokine. These data advance our understanding of how MIF regulates inflammation and identify it as a factor critical for NLRP3 inflammasome activation.
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