Abstract |
B-cell activating factor (BAFF) is a potent cell-survival factor expressed in many haematopoietic cells. BAFF regulates B-cell survival, differentiation and proliferation by binding to three tumour necrosis factor receptors: transmembrane activator, calcium modulator and cyclophilin ligand interactor; B-cell maturation antigen; and BAFF receptor (BAFF-R). Although BAFF-R is produced by interferon gamma (IFN-γ), the underlying mechanism remains elusive. In this study, we examined the effects of IFN-γ on BAFF-R expression in cultured human multiple myeloma cells (KM3) both at the transcriptional and posttranscriptional levels. Incubation of KM3 cells with IFN-γ elevated the expression of BAFF-R mRNA and protein levels. IFN-γ elicited marked enhancement of the human BAFF-R promoter activity and nuclear factor kappa B (NF-κB) DNA binding activity. NF-κB dependent on the human BAFF-R gene might be regulated via a transcriptional event through one putative NF-κB site on the BAFF-R gene promoter. These results provide a molecular mechanism for the increase in expression of the BAFF-R gene that is induced by proinflammatory cytokines in responsive cells.
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Authors | Xianjuan Shen, Xia Zhang, Guang Xu, Shaoqing Ju |
Journal | Cell biochemistry and function
(Cell Biochem Funct)
Vol. 29
Issue 6
Pg. 513-20
(Aug 2011)
ISSN: 1099-0844 [Electronic] England |
PMID | 21744373
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2011 John Wiley & Sons, Ltd. |
Chemical References |
- Antiviral Agents
- B-Cell Activation Factor Receptor
- NF-kappa B
- RNA, Messenger
- Interferon-gamma
- DNA
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Topics |
- Antiviral Agents
(pharmacology)
- B-Cell Activation Factor Receptor
(genetics, metabolism)
- Binding Sites
- DNA
(metabolism)
- Gene Expression Regulation, Archaeal
(drug effects)
- Humans
- Interferon-gamma
(pharmacology)
- Multiple Myeloma
(metabolism)
- NF-kappa B
(metabolism)
- Promoter Regions, Genetic
- RNA, Messenger
(metabolism)
- Signal Transduction
- Tumor Cells, Cultured
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