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Involvement of Fcα/μR (CD351) in autoantibody production

机译:Fcα/μR(CD351)与自身抗体的产生有关

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摘要

Antibody exerts various immune responses via binding to Fc receptors expressed on immune cells. Although several reports have demonstrated that IgM prevents autoantibody production, the role of IgM Fc receptors is largely unknown. To analyze the involvement of Fcα/μR (CD351), an Fc receptor for IgM and IgA expressed on B cells and follicular dendritic cells (FDCs), in IgM-mediated suppression of autoantibody production, we generated mice deficient in Fcα/μR on the background of MRL/MpJ-Faslpr/lpr (Fcamr-/-Faslpr/lpr) mice. Fcamr-/-Faslpr/lpr mice showed significantly lower titers of IgG autoantibodies against double strand (ds) DNA, histone and cardiolipin in the sera than did Fcamr+/+Faslpr/lpr mice. Moreover, Fcamr-/-Faslpr/lpr mice showed higher survival rate at the ages of 28, 32 and 40 weeks old, compared with Fcamr+/+Faslpr/lpr mice. These results suggest that Fcα/μR enhances, rather than suppresses, autoantibody production.
机译:抗体通过与免疫细胞上表达的Fc受体结合而发挥各种免疫反应。尽管一些报道表明IgM可以阻止自身抗体的产生,但是IgM Fc受体的作用在很大程度上尚不清楚。为了分析Fcα/μR(CD351)(在B细胞和滤泡树突状细胞(FDC)上表达的IgM和IgA的Fc受体)在IgM介导的自身抗体产生的抑制中的作用,我们在小鼠上产生了Fcα/μR缺陷的小鼠。 MRL / MpJ-Faslpr / lpr(Fcamr-/-Faslpr / lpr)小鼠的背景。与Fcamr + / + Faslpr / lpr小鼠相比,Fcamr-/-Faslpr / lpr小鼠的血清中针对双链(ds)DNA,组蛋白和心磷脂的IgG自身抗体的滴度明显更低。此外,与Fcamr + / + Faslpr / lpr小鼠相比,Fcamr-/-Faslpr / lpr小鼠在28、32和40周龄时显示出更高的存活率。这些结果表明Fcα/μR增强而不是抑制自身抗体的产生。

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