| Literature DB >> 15485634 |
Youcun Qian1, Jinzhong Qin, Grace Cui, Mayumi Naramura, E Charles Snow, Carl F Ware, Robert L Fairchild, Sidne A Omori, Robert C Rickert, Martin Scott, Brian L Kotzin, Xiaoxia Li.
Abstract
TNF receptor (TNFR) superfamily members, CD40, and BAFFR play critical roles in B cell survival and differentiation. Genetic deficiency in a novel adaptor molecule, Act1, for CD40 and BAFF results in a dramatic increase in peripheral B cells, which culminates in lymphadenopathy and splenomegaly, hypergammaglobulinemia, and autoantibodies. While the B cell-specific Act1 knockout mice displayed a similar phenotype with less severity, the pathology of the Act1-deficient mice was mostly blocked in CD40-Act1 and BAFF-Act1 double knockout mice. CD40- and BAFF-mediated survival is significantly increased in Act1-deficent B cells, with stronger IkappaB phosphorylation, processing of NF-kappaB2 (p100/p52), and activation of JNK, ERK, and p38 pathways, indicating that Act1 negatively regulates CD40- and BAFF-mediated signaling events. These findings demonstrate that Act1 plays an important role in the homeostasis of B cells by attenuating CD40 and BAFFR signaling.Entities:
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Year: 2004 PMID: 15485634 DOI: 10.1016/j.immuni.2004.09.001
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745