NF-kappaB activation by protein kinase C isoforms and B-cell function

EMBO Rep. 2003 Jan;4(1):31-6. doi: 10.1038/sj.embor.embor704.

Abstract

B cells are essential to the immune response in health and disease. Results from knockout (KO) mice for different members of the nuclear factor-kappaB (NF-kappaB) family have highlighted the importance of this transcription factor in B cell development and function. The recent generation of additional KO mice for adapters and kinases implicated in NF-kappaB activation, including several protein kinase C isoforms, has provided new insights into the roles of these proteins in B cell signalling. These studies have also given rise to a number of important questions that must be answered with further experimentation to establish accurately the signalling pathways that regulate B-cell function through NF-kappaB.

Publication types

  • Review

MeSH terms

  • Animals
  • Apoptosis
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • Gene Expression Regulation
  • Humans
  • I-kappa B Kinase
  • Isoenzymes / physiology
  • Macromolecular Substances
  • Mice
  • Mice, Knockout
  • Models, Biological
  • NF-kappa B / deficiency
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • Phosphorylation
  • Protein Kinase C / physiology*
  • Protein Processing, Post-Translational
  • Protein Serine-Threonine Kinases / physiology
  • Protein Subunits
  • Receptors, Antigen, B-Cell / physiology*
  • Signal Transduction
  • Transcription, Genetic

Substances

  • Isoenzymes
  • Macromolecular Substances
  • NF-kappa B
  • Protein Subunits
  • Receptors, Antigen, B-Cell
  • Protein Serine-Threonine Kinases
  • CHUK protein, human
  • Chuk protein, mouse
  • I-kappa B Kinase
  • IKBKB protein, human
  • IKBKE protein, human
  • Ikbkb protein, mouse
  • Ikbke protein, mouse
  • Protein Kinase C