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BAFF-R gene induced by IFN-γ in multiple myeloma cells is related to NF-κB signals.

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.
AuthorsXianjuan Shen, Xia Zhang, Guang Xu, Shaoqing Ju
JournalCell biochemistry and function (Cell Biochem Funct) Vol. 29 Issue 6 Pg. 513-20 (Aug 2011) ISSN: 1099-0844 [Electronic] England
PMID21744373 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2011 John Wiley & Sons, Ltd.
Chemical References
  • Antiviral Agents
  • B-Cell Activation Factor Receptor
  • NF-kappa B
  • RNA, Messenger
  • Interferon-gamma
  • DNA
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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