B细胞激活因子
受体
肿瘤坏死因子受体
细胞生物学
肿瘤坏死因子α
免疫学
生物
抗体
B细胞
遗传学
作者
Jeffrey S. Thompson,Sarah A. Bixler,Fang Qian,Kalpit A. Vora,Martin Scott,Teresa G. Cachero,Catherine Hession,Pascal Schneider,Irene Sizing,Colleen Mullen,Kathy Strauch,Mohammad Zafari,Christopher D. Benjamin,Jürg Tschopp,Jeffrey L. Browning,Christine Ambrose
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2001-09-14
卷期号:293 (5537): 2108-2111
被引量:886
标识
DOI:10.1126/science.1061965
摘要
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.
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