首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Altered expression of signalling lymphocyte activation molecule (SLAM) family receptors CS1 (CD319) and 2B4 (CD244) in patients with systemic lupus erythematosus
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Altered expression of signalling lymphocyte activation molecule (SLAM) family receptors CS1 (CD319) and 2B4 (CD244) in patients with systemic lupus erythematosus

机译:系统性红斑狼疮患者的信号淋巴细胞活化分子(SLAM)家族受体CS1(CD319)和2B4(CD244)的表达改变

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摘要

CS1 (CRACC, CD319) and 2B4 (CD244), members of the signalling lymphocyte activation molecule (SLAM) family receptors, regulate various immune functions. Genes encoding SLAM family receptors are located at 1q23, implicated in systemic lupus erythematosus (SLE). In this study, we have investigated the expression and alternative splicing of CS1 and 2B4 in immune cells from SLE patients. The surface expression of CS1 and 2B4 on total peripheral blood mononuclear cells (PBMCs), T, B, natural killer (NK) cells and monocytes in 45 patients with SLE and 30 healthy individuals was analysed by flow cytometry. CS1-positive B cell population was increased significantly in SLE patients. Because CS1 is a self-ligand and homophilic interaction of CS1 induces B cell proliferation and autocrine cytokine secretion, this could account for autoreactive B cell proliferation in SLE. The proportion of NK cells and monocytes expressing 2B4 on their surface was significantly lower in patients with SLE compared to healthy controls. Our study demonstrated altered expression of splice variants of CS1 and 2B4 that mediate differential signalling in PBMC from patients with SLE.
机译:CS1(CRACC,CD319)和2B4(CD244),信号淋巴细胞活化分子(SLAM)家族受体的成员,调节着各种免疫功能。编码SLAM家族受体的基因位于1q23,与系统性红斑狼疮(SLE)有关。在这项研究中,我们研究了SLE患者免疫细胞中CS1和2B4的表达和选择性剪接。通过流式细胞术分析了45名SLE患者和30名健康个体的总外周血单核细胞(PBMC),T,B,自然杀伤(NK)细胞和单核细胞中CS1和2B4的表面表达。 SLE患者中CS1阳性B细胞数量显着增加。因为CS1是自配体,并且CS1的同质相互作用诱导B细胞增殖和自分泌细胞因子分泌,所以这可以解释SLE中自身反应性B细胞增殖。与健康对照组相比,SLE患者的NK细胞和单核细胞表面表达2B4的比例显着降低。我们的研究表明,SLE患者的PBMC中介导差异信号的CS1和2B4剪接变体的表达有所改变。

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