BAFF-R, a newly identified TNF receptor that specifically interacts with BAFF.


Autoria(s): Thompson J.S.; Bixler S.A.; Qian F.; Vora K.; Scott M.L.; Cachero T.G.; Hession C.; Schneider P.; Sizing I.D.; Mullen C.; Strauch K.; Zafari M.; Benjamin C.D.; Tschopp J.; Browning J.L.; Ambrose C.
Data(s)

2001

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_780872DAEDF2

isbn:0036-8075 (Print)

pmid:11509692

doi:10.1126/science.1061965

isiid:000171028700079

Idioma(s)

en

Fonte

Science, vol. 293, no. 5537, pp. 2108-2111

Palavras-Chave #Amino Acid Sequence; Animals; B-Cell Activating Factor; B-Cell Activation Factor Receptor; B-Cell Maturation Antigen; B-Lymphocytes/immunology; B-Lymphocytes/metabolism; Cell Line; Chromosome Mapping; Chromosomes, Human, Pair 22; Cloning, Molecular; Homeostasis; Humans; Ligands; Lymphoid Tissue/metabolism; Male; Membrane Proteins/metabolism; Mice; Mice, Inbred A; Mice, Inbred C57BL; Molecular Sequence Data; RNA, Messenger/chemistry; RNA, Messenger/genetics; Receptors, Tumor Necrosis Factor/chemistry; Receptors, Tumor Necrosis Factor/genetics; Recombinant Fusion Proteins/metabolism; Signal Transduction; Transfection; Transmembrane Activator and CAML Interactor Protein; Tumor Necrosis Factor-alpha/metabolism
Tipo

info:eu-repo/semantics/article

article