Haas K M, Estes D M
Department of Molecular Microbiology and Immunology, School of Medicine, College of Veterinary Medicine, University of Missouri-Columbia, Columbia, MO 65211, USA.
Immunology. 2000 Feb;99(2):272-8. doi: 10.1046/j.1365-2567.2000.00962.x.
Experiments reported herein demonstrate that activation of bovine B cells via surface immunoglobulin M (sIgM) cross-linking, analogous to T-cell independent (TI-2) antigenic stimulation, results in the expression of CD5. Interestingly, in the presence of CD40 ligand, sIgM-mediated induction of CD5 on B cells was inhibited. These findings indicate that activation of bovine B cells via B-cell receptor (BCR) cross-linking results in a CD5+ B-cell phenotype and that CD40 signalling is inhibitory to this process. Analysis of cytokine mRNA indicates that bovine B cells constitutively express tumour necrosis factor-alpha (TNF-alpha) and interleukin (IL)-1beta transcripts in vitro, while IL-10 mRNA expression is induced following sIgM cross-linking. IL-12 p40 transcripts were produced by B cells activated by CD40, but not by BCR, ligation. Analysis of cytokine receptor mRNA indicates that activation through CD40, in the presence or absence of IgM cross-linking, results in increased IL-4 receptor-alpha (IL-4Ralpha), IL-13Ralpha1 and interferon-alpha receptor 1 (IFN-alphaR1) mRNA levels. Overall, these findings suggest that activation of bovine B cells through BCR cross-linking yields an activation phenotype that differs substantially from that of B cells activated through CD40.
本文报道的实验表明,通过表面免疫球蛋白M(sIgM)交联激活牛B细胞,类似于T细胞非依赖性(TI-2)抗原刺激,会导致CD5的表达。有趣的是,在存在CD40配体的情况下,sIgM介导的B细胞上CD5的诱导受到抑制。这些发现表明,通过B细胞受体(BCR)交联激活牛B细胞会导致CD5+B细胞表型,并且CD40信号传导对这一过程具有抑制作用。细胞因子mRNA分析表明,牛B细胞在体外组成性表达肿瘤坏死因子-α(TNF-α)和白细胞介素(IL)-1β转录本,而sIgM交联后会诱导IL-10 mRNA表达。IL-12 p40转录本由CD40激活的B细胞产生,但不由BCR连接激活的B细胞产生。细胞因子受体mRNA分析表明,在存在或不存在IgM交联的情况下,通过CD40激活会导致IL-4受体-α(IL-4Rα)、IL-13Rα1和干扰素-α受体1(IFN-αR1)mRNA水平升高。总体而言,这些发现表明,通过BCR交联激活牛B细胞会产生一种与通过CD40激活的B细胞有很大不同的激活表型。