| Literature DB >> 26773039 |
Jonathan V Almaden1, Yi C Liu2, Edward Yang3, Dennis C Otero3, Harry Birnbaum4, Jeremy Davis-Turak1, Masataka Asagiri5, Michael David3, Ananda W Goldrath3, Alexander Hoffmann2.
Abstract
Targeted deletion of BAFF causes severe deficiency of splenic B cells. BAFF-R is commonly thought to signal to nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB)-inducing kinase dependent noncanonical NF-κB RelB. However, RelB-deficient mice have normal B-cell numbers. Recent studies showed that BAFF also signals to the canonical NF-κB pathway, and we found that both RelB and cRel are persistently activated, suggesting BAFF signaling coordinates both pathways to ensure robust B-cell development. Indeed, we report now that combined loss of these 2 NF-κB family members leads to impaired BAFF-mediated survival and development in vitro. Although single deletion of RelB and cRel was dispensable for normal B-cell development, double knockout mice displayed an early B-cell developmental blockade and decreased mature B cells. Despite disorganized splenic architecture in Relb(-/-)cRel(-/-) mice, generation of mixed-mouse chimeras established the developmental phenotype to be B-cell intrinsic. Together, our results indicate that BAFF signals coordinate both RelB and cRel activities to ensure survival during peripheral B-cell maturation.Entities:
Mesh:
Substances:
Year: 2016 PMID: 26773039 PMCID: PMC4786837 DOI: 10.1182/blood-2014-10-606988
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113