| Literature DB >> 24239354 |
Julia Jellusova1, Ana V Miletic, Matthew H Cato, Wai-Wai Lin, Yinling Hu, Gail A Bishop, Mark J Shlomchik, Robert C Rickert.
Abstract
BAFF is a soluble factor required for B cell maturation and survival. BAFF-R signals via the noncanonical NF-κB 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.Entities:
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Year: 2013 PMID: 24239354 PMCID: PMC3887557 DOI: 10.1016/j.celrep.2013.10.022
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423