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.
MeSH terms
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Animals
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Apoptosis
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B-Lymphocytes / cytology
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B-Lymphocytes / immunology*
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Gene Expression Regulation
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Humans
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I-kappa B Kinase
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Isoenzymes / physiology
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Macromolecular Substances
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Mice
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Mice, Knockout
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Models, Biological
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NF-kappa B / deficiency
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NF-kappa B / genetics
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NF-kappa B / metabolism*
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Phosphorylation
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Protein Kinase C / physiology*
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Protein Processing, Post-Translational
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Protein Serine-Threonine Kinases / physiology
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Protein Subunits
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Receptors, Antigen, B-Cell / physiology*
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Signal Transduction
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Transcription, Genetic
Substances
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Isoenzymes
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Macromolecular Substances
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NF-kappa B
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Protein Subunits
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Receptors, Antigen, B-Cell
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Protein Serine-Threonine Kinases
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CHUK protein, human
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Chuk protein, mouse
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I-kappa B Kinase
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IKBKB protein, human
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IKBKE protein, human
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Ikbkb protein, mouse
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Ikbke protein, mouse
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Protein Kinase C