T-cell-expressed proprotein convertase furin is essential for maintenance of peripheral immune tolerance

被引:169
作者
Pesu, Marko [1 ]
Watford, Wendy T. [1 ]
Wei, Lai [1 ]
Xu, Lili [2 ]
Fuss, Ivan [2 ]
Strober, Warren [2 ]
Andersson, John [3 ]
Shevach, Ethan M. [3 ]
Quezado, Martha [5 ]
Bouladoux, Nicolas [4 ]
Roebroek, Anton [6 ,7 ]
Belkaid, Yasmine [4 ]
Creemers, John [6 ,7 ]
O'Shea, John J. [1 ]
机构
[1] NIAMSD, Mol Immunol & Inflammat Branch, NIH, Bethesda, MD 20892 USA
[2] NIAID, Mucosal Immun Sect, Host Def Lab, NIH, Bethesda, MD 20892 USA
[3] NIAID, Cellular Immunol Sect, Immunol Lab, NIH, Bethesda, MD 20892 USA
[4] NIAID, Mucosal Immunol Unit, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[5] NCI, Pathol Lab, NIH, Bethesda, MD 20892 USA
[6] Katholieke Univ Leuven, Biochem Neuroendocrinol Lab, B-3000 Louvain, Belgium
[7] VIB, B-3000 Louvain, Belgium
基金
芬兰科学院;
关键词
D O I
10.1038/nature07210
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Furin is one of seven proprotein convertase family members that promote proteolytic maturation of proproteins(1). It is induced in activated T cells and is reported to process a variety of substrates including the anti- inflammatory cytokine transforming growth factor (TGF)-beta 1 ( refs 2 - 4), but the non- redundant functions of furin versus other proprotein convertases in T cells are unclear. Here we show that conditional deletion of furin in T cells allowed for normal T- cell development but impaired the function of regulatory and effector T cells, which produced less TGF-beta 1. Furin-deficient T regulatory (T-reg) cells were less protective in a T- cell transfer colitis model and failed to induce Foxp3 in normal T cells. Additionally, furin- deficient effector cells were inherently over-active and were resistant to suppressive activity of wild- type T-reg cells. Thus, our results indicate that furin is indispensable in maintaining peripheral tolerance, which is due, at least in part, to its non- redundant, essential function in regulating TGF-beta 1 production. Targeting furin has emerged as a strategy in malignant and infectious disease(5,6). Our results suggest that inhibiting furin might activate immune responses, but may result in a breakdown in peripheral tolerance.
引用
收藏
页码:246 / U73
页数:6
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