Context-Specific BAFF-R Signaling by the NF-κB and PI3K Pathways

被引:66
|
作者
Jellusova, Julia [1 ]
Miletic, Ana V. [1 ]
Cato, Matthew H. [1 ]
Lin, Wai-Wai [2 ,3 ]
Hu, Yinling [6 ]
Bishop, Gail A. [2 ,3 ,4 ,5 ]
Shlomchik, Mark J. [7 ]
Rickert, Robert C. [1 ]
机构
[1] Sanford Burnham Med Res Inst, Infect & Inflammatory Dis Ctr, Program Inflammatory Dis, La Jolla, CA 92037 USA
[2] Univ Iowa, Grad Program Immunol, Iowa City, IA 52242 USA
[3] VA Med Ctr, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
[5] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[6] NCI, Canc & Inflammat Program, Ctr Canc Res, NIH, Frederick, MD 21701 USA
[7] Univ Pittsburgh, Sch Med, Dept Immunol, Pittsburgh, PA 15261 USA
来源
CELL REPORTS | 2013年 / 5卷 / 04期
基金
新加坡国家研究基金会;
关键词
CELL SURVIVAL; CUTTING EDGE; IKK-ALPHA; RECEPTOR SIGNALS; PHOSPHATIDYLINOSITOL; 3-KINASE; T-LYMPHOCYTES; MARGINAL ZONE; ACTIVATION; MATURE; DIFFERENTIATION;
D O I
10.1016/j.celrep.2013.10.022
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
BAFF is a soluble factor required for B cell maturation and survival. BAFF-R signals via the noncanonical NF-kappa B pathway regulated by the TRAF3/NIK/IKK1 axis. We show that deletion of Ikk1 during early B cell development causes a partial impairment in B cell maturation and BAFF-dependent survival, but inactivation of Ikk1 in mature B cells does not affect survival. We further show that BAFF-R employs CD19 to promote survival via phosphatidylinositol 3-kinase (PI3K), and that coinactivation of Cd19 and Ikk1 causes a profound block in B cell maturation at the transitional stage. Consistent with a role for PI3K in BAFF-R function, inactivation of PTEN mediates a partial rescue of B cell maturation and function in Baff(-/-) animals. Elevated PI3K signaling also circumvents BAFF-dependent survival in a spontaneous B cell lymphoma model. These findings indicate that the combined activities of PI3K and IKK1 drive peripheral B cell differentiation and survival in a context-dependent manner.
引用
收藏
页码:1022 / 1035
页数:14
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