Ndfip1 protein promotes the function of itch ubiquitin ligase to prevent T cell activation and T helper 2 cell-mediated inflammation

被引:115
|
作者
Oliver, Paula M.
Cao, Xiao
Scott Worthen, George
Shi, Peijun
Briones, Natalie
MacLeod, Megan
White, Janice
Kirby, Patricia
Kappler, John
Marrack, Philippa
Yang, Baoli [1 ]
机构
[1] Univ Iowa, Dept Obstet & Gynecol, Carver Coll Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pathol, Carver Coll Med, Iowa City, IA 52242 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO 80206 USA
[4] Natl Jewish Med & Res Ctr, Howard Hughes Med Inst, Denver, CO 80206 USA
[5] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80206 USA
[6] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol, Denver, CO 80206 USA
[7] Univ Colorado, Hlth Sci Ctr, Dept Biochem & Mol Genet, Denver, CO 80206 USA
关键词
D O I
10.1016/j.immuni.2006.10.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nedd4 family interacting protein-1 (Ndfip1) is a protein whose only known function is that it binds Nedd4, a HECT-type E3 ubiquitin ligase. Here we show that mice lacking Ndfip1 developed severe inflammation of the skin and lung and died prematurely. This condition was due to a defect in Ndfip1(-/-) T cells. Ndfip1(-/-) cells were activated, and they proliferated and adopted a T helper 2 (Th2) phenotype more readily than did their Ndfip1(+/+) counterparts. This phenotype resembled that of Itchy mutant mice, suggesting that Ndfip1 might affect the function of Itch, an E3 ubiquitin ligase. We show that T cell activation promoted both Ndfip1 expression and its association with Itch. In the absence of Ndfip1, JunB half-life was prolonged after T cell activation. Thus, in the absence of Ndfip1, Itch is inactive and JunB accumulates. As a result, T cells produce Th2 cytokines and promote Th2-mediated inflammatory disease.
引用
收藏
页码:929 / 940
页数:12
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