Abstract
B cell homeostasis has been shown to critically depend on BAFF, the B cell activation factor from the tumor necrosis factor (TNF) family. Although BAFF is already known to bind two receptors, BCMA and TACI, we have identified a third receptor for BAFF that we have termed BAFF-R. BAFF-R binding appears to be highly specific for BAFF, suggesting a unique role for this ligand-receptor interaction. Consistent with this, the BAFF-R locus is disrupted in A/WySnJ mice, which display a B cell phenotype qualitatively similar to that of the BAFF-deficient mice. Thus, BAFF-R appears to be the principal receptor for BAFF-mediated mature B cell survival.
MeSH terms
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Amino Acid Sequence
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Animals
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B-Cell Activating Factor
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B-Cell Activation Factor Receptor
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B-Cell Maturation Antigen
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B-Lymphocytes / immunology
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B-Lymphocytes / metabolism
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B-Lymphocytes / physiology*
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Cell Line
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Chromosome Mapping
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Chromosomes, Human, Pair 22
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Cloning, Molecular
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Homeostasis
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Humans
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Ligands
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Lymphoid Tissue / metabolism
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Male
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Membrane Proteins / metabolism*
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Mice
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Mice, Inbred A
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Mice, Inbred C57BL
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Molecular Sequence Data
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RNA, Messenger / chemistry
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Receptors, Tumor Necrosis Factor / chemistry
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Receptors, Tumor Necrosis Factor / genetics
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Receptors, Tumor Necrosis Factor / metabolism*
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Recombinant Fusion Proteins / metabolism
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Signal Transduction
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Transfection
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Transmembrane Activator and CAML Interactor Protein
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Tumor Necrosis Factor-alpha / metabolism*
Substances
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B-Cell Activating Factor
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B-Cell Activation Factor Receptor
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B-Cell Maturation Antigen
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Ligands
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Membrane Proteins
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RNA, Messenger
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Receptors, Tumor Necrosis Factor
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Recombinant Fusion Proteins
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TNFRSF13B protein, human
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TNFRSF13C protein, human
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TNFRSF17 protein, human
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TNFSF13B protein, human
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Tnfrsf13b protein, mouse
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Tnfrsf13c protein, mouse
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Tnfrsf17 protein, mouse
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Tnfsf13b protein, mouse
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Transmembrane Activator and CAML Interactor Protein
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Tumor Necrosis Factor-alpha