| Literature DB >> 12352969 |
Estefania Claudio1, Keith Brown, Sun Park, Hongshan Wang, Ulrich Siebenlist.
Abstract
NF-kappa B is usually activated by signal-induced, ubiquitin-mediated degradation of its inhibitor, I kappa B. This process is initiated by phosphorylation of I kappa B by the I kappa B kinase (IKK) complex, predominantly by the IKK beta catalytic subunit, and requires the regulatory subunit IKK gamma (NEMO). Another activation pathway, with no known physiological inducers, involves ubiquitin-mediated processing of the NF-kappa B2 inhibitory protein p100 and is dependent on phosphorylation of p100 by IKK alpha. We show here that B cell-activating factor (BAFF) activates this second pathway and that this requires the BAFF receptor (BAFF-R), the NF-kappa B-inducing kinase (NIK) and protein synthesis, but not NEMO. This NEMO-independent cascade is physiologically relevant for the survival and, hence, progression of maturing splenic B cells.Entities:
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Year: 2002 PMID: 12352969 DOI: 10.1038/ni842
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606