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首页> 外文期刊>The FASEB Journal >Expansion of an osteopontin-expressing T follicular helper cell subset correlates with autoimmunity in B6.Sle1b mice and is suppressed by the H1-isoform of the Slamf6 receptor
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Expansion of an osteopontin-expressing T follicular helper cell subset correlates with autoimmunity in B6.Sle1b mice and is suppressed by the H1-isoform of the Slamf6 receptor

机译:表达骨桥蛋白的T卵泡辅助细胞群的扩张与B6.SLE1B小鼠的自身免疫相关,并且由SLAMF6受体的H1-同种型抑制

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摘要

The costimulatory receptor Slamf6 partially controls lupus-related autoimmunity in congenic Sle1b mice; for instance, the presence of the protein isoform Slamf6-H1 in Sle1b.Slamf6-H1 mice mitigates disease. Here, we report that young Sle1b mice, but not Sle1b.Slamf6-H1 or B6 mice, contain a memory T-helper cell subset identified by ]mt]2-fold increase in expression of 17 genes, chief among which is Spp1, encoding the cytokine osteopontin (OPN). These T follicular helper (TFH) cells, including OPN+ TFH cells, expand concomitantly with severity of the disease. By contrast, Sle1b.Slamf6-H1 or Sle1b.SAP?/? mice do not develop autoantibodies and the number of TFH cells is 5 times lower than in age-matched Sle1b mice. By comparing Sle1b and Sle1b.OPN?/? mice, we find that the lack of OPN expression impedes early autoantibody production. Furthermore, on the adoptive transfer of Sle1b.OPN?/? CD4+ T cells into bm12 recipients autoantibody production and germinal center formation is reduced compared to recipients of Sle1b.OPN+/+ CD4+ T cells. We propose a model in which OPN provides a survival signal for a precursor TFH cell subset, which is a key factor in autoimmunity. Keszei, M., Detre, C., Castro, W., Magelky, E., O'Keeffe, M., Kis-Toth, K., Tsokos, G. C., Wang, N., Terhorst, C. Expansion of an osteopontin-expressing T follicular helper cell subset correlates with autoimmunity in B6.Sle1b mice and is suppressed by the H1-isoform of the Slamf6 receptor.
机译:刺激受体Slamf6部分地控制了与Congenic SER1B小鼠中的狼疮相关的自身免疫性;例如,在SLE1b.slamf6-h1小鼠中,蛋白质同种型Slamf6-H1的存在减轻疾病。在这里,我们报告的是,幼小的SER1B小鼠,但不是SLE1B.Slamf6-H1或B6小鼠含有由17个基因表达的MT的2倍的内存T-辅助细胞子集,其主要是SPP1,编码细胞因子骨桥蛋白(OPN)。这些T卵泡辅助助剂(TFH)细胞,包括OPN + TFH细胞,伴随着疾病的严重程度。相比之下,sle1b.slamf6-h1或sle1b.sap ?/?小鼠不会发展自身抗体,TFH细胞的数量比年龄匹配的SER1B小鼠低5倍。通过比较sle1b和sle1b.opn?/?小鼠,我们发现缺乏OPN表达阻碍了早期的自身抗体生产。此外,在养款的过度转移上?/?与SLE1B.OPN + / + CD4 + T细胞的接受者相比,CD4 + T细胞自身抗体产生和生发中心形成减少。我们提出了一种模型,其中OPN为前体TFH小区子集提供生存信号,这是自身免疫的关键因素。 Keszei,M.,Detre,C.,Castro,W.,Magelky,E.,O'Keeffe,M.,Kis-Toth,K。,Tsokos,GC,王,N.,Terhorst,C.扩建表达骨桥蛋白的T滤泡辅助细胞群与B6.SLE1B小鼠中的自身免疫相关,并且由SLAMF6受体的H1-同种型抑制。

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