首页> 外文期刊>Scandinavian journal of immunology. >Human Soluble CD80 is generated by alternative splicing, and recombinant soluble CD80 binds to CD28 and CD152 influencing T-cell activation.
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Human Soluble CD80 is generated by alternative splicing, and recombinant soluble CD80 binds to CD28 and CD152 influencing T-cell activation.

机译:人可溶性CD80是通过选择性剪接产生的,重组可溶性CD80与影响T细胞活化的CD28和CD152结合。

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CD80 is a costimulatory factor mainly expressed on the surface of activated monocytes, B cells and dendritic cells. In this study, we demonstrate that 24% of healthy individuals have soluble forms of CD80, sCD80, in their serum. The concentration of sCD80 ranged from 0 to 1 mg/l. At the mRNA level, we detected a spliced form s1CD80 (771 bp), in unstimulated monocytes and B cells, while another form named s2CD80 (489 bp) was expressed in activated T cells as well as in freshly isolated and activated monocytes. s1CD80 lacks the transmembrane domain, and the IgC-like domain plus the transmembrane domain are spliced out of s2CD80. We also present data demonstrating that recombinant s1CD80 binds to recombinant CD152-Ig and CD28-Ig. It can also bind to T cells, preferentially to activated T cells. Recombinant sCD80 had immunomodulatory effects shown by its inhibition of the mixed lymphocyte reaction and inhibition of T-cell proliferation. sCD80 in human serum adds a new member to the family of soluble receptors, implying a network of soluble costimulatory factors with functional relevance. The inhibitory effect of the recombinant protein on T-cell activation makes it a possible candidate for treatment of diseases associated with hyperactivated T cells.
机译:CD80是主要在活化的单核细胞,B细胞和树突状细胞的表面表达的共刺激因子。在这项研究中,我们证明了24%的健康个体在其血清中具有可溶形式的CD80,sCD80。 sCD80的浓度范围为0至1 mg / l。在mRNA水平上,我们在未刺激的单核细胞和B细胞中检测到剪接形式s1CD80(771 bp),而另一种名为s2CD80(489 bp)的形式在活化T细胞以及新鲜分离和活化的单核细胞中表达。 s1CD80缺少跨膜结构域,并且从s2CD80中剪接了IgC样结构域和跨膜结构域。我们还提供了证明重组s1CD80与重组CD152-Ig和CD28-Ig结合的数据。它也可以结合T细胞,优先结合活化的T细胞。重组sCD80具有抑制混合淋巴细胞反应和抑制T细胞增殖的免疫调节作用。人血清中的sCD80为可溶性受体家族增添了一个新成员,这意味着具有功能相关性的可溶性共刺激因子网络。重组蛋白对T细胞活化的抑制作用使其成为治疗与超活化T细胞有关的疾病的可能候选者。

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