Rediscovering MIF: New Tricks for an Old Cytokine

被引:71
作者
Harris, James [1 ]
VanPatten, Sonya [2 ]
Deen, Nadia S. [1 ]
Al-Abed, Yousef [2 ]
Morand, Eric F. [1 ]
机构
[1] Monash Univ, Monash Hlth, Sch Clin Sci, Rheumatol Grp,Ctr Inflammatory Dis, Clayton, Vic, Australia
[2] Feinstein Inst Med Res, Ctr Mol Innovat, Manhasset, NY USA
基金
英国医学研究理事会;
关键词
MIGRATION-INHIBITORY FACTOR; NLRP3 INFLAMMASOME ACTIVATION; FACTOR GENE; D-DOPACHROME; MOUSE MODEL; K+ EFFLUX; PROTEIN; POLYMORPHISMS; EXPRESSION; INTERACTS;
D O I
10.1016/j.it.2019.03.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Produced by many cell types, macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine with critical and supporting roles in many disease states and conditions. Its disease associations, myriad functions, receptors, and downstream signaling have been the subject of considerable research, yet many questions remain. Moreover, the relevance of MIF's partially functionally redundant family member, D-dopachrome tautomerase (D-DT), also remains to be further characterized. Here, we discuss recent discoveries demonstrating direct roles of MIF in supporting NLR Family Pyrin Domain-Containing 3 (NRLP3) inflammasome activation, as well as acting as a molecular chaperone for intracellular proteins. These findings may offer new clues to understanding MIF's multiple functions, and assist the development of putative MIF-targeting therapeutics for a variety of pathologies.
引用
收藏
页码:447 / 462
页数:16
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