Yang Yang, Liu Xikui K, Nguyen Thang, Bishop Caroline, Graf Daniel, Dong Chen
Department of Immunology, University of Washington, Seattle, WA 98195, USA.
J Immunol. 2007 Mar 15;178(6):3661-7. doi: 10.4049/jimmunol.178.6.3661.
T cell activation by APCs is regulated by B7-like costimulatory molecules. In this study, we describe a new B7 superfamily member, B7S3, with two differentially spliced isoforms expressed in lymphoid and nonlymphoid tissues. A soluble B7S3-Ig protein bound to professional APC constitutively as well as to activated but not naive T cells. B7S3-Ig treatment greatly inhibited T cell proliferation and IL-2 production. B7S3-Ig also reduced cytokine production by effector T cells. Interestingly, although human genome appears to contain a single-copy B7S3 homolog, the mouse B7S3 gene has 10 relatives within a 2-Mb region constituting a B7S3 gene family. This study identifies B7S3 as a novel negative regulator of T cells, and suggests evolutionarily divergent T cell regulation mechanisms in mammals.
抗原呈递细胞(APC)对T细胞的激活受B7样共刺激分子调控。在本研究中,我们描述了一种新的B7超家族成员B7S3,它有两种不同剪接的异构体,在淋巴组织和非淋巴组织中表达。可溶性B7S3-Ig蛋白可组成性地结合专职APC,也可结合活化的T细胞,但不结合未活化的T细胞。B7S3-Ig处理可极大地抑制T细胞增殖和白细胞介素-2的产生。B7S3-Ig还可减少效应T细胞的细胞因子产生。有趣的是,尽管人类基因组似乎包含一个单拷贝的B7S3同源物,但小鼠B7S3基因在一个2兆碱基区域内有10个相关基因,构成了一个B7S3基因家族。本研究将B7S3鉴定为T细胞的一种新型负调节因子,并提示哺乳动物中T细胞调节机制存在进化上的差异。