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Context-specific BAFF-R signaling by the NF-κB and PI3K pathways.
Jellusova, Julia; Miletic, Ana V; Cato, Matthew H; Lin, Wai-Wai; Hu, Yinling; Bishop, Gail A; Shlomchik, Mark J; Rickert, Robert C.
Affiliation
  • Jellusova J; Program on Inflammatory Diseases, Infectious and Inflammatory Diseases Center, Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Cell Rep ; 5(4): 1022-35, 2013 Nov 27.
Article in En | MEDLINE | ID: mdl-24239354
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphatidylinositol 3-Kinases / Lymphopoiesis / I-kappa B Kinase / B-Cell Activating Factor Type of study: Prognostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2013 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphatidylinositol 3-Kinases / Lymphopoiesis / I-kappa B Kinase / B-Cell Activating Factor Type of study: Prognostic_studies Limits: Animals Language: En Journal: Cell Rep Year: 2013 Document type: Article Affiliation country: United States Country of publication: United States