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CXCL13 Promotes Proliferation of Mesangial Cells by Combination with CXCR5 in SLE

机译:CXCL13通过与SLE中的CXCR5结合促进系膜细胞增殖

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摘要

As a CXC subtype member of the chemokine superfamily, CXCL13 is considered to be involved in systemic lupus erythematosus (SLE), especially in lupus nephritis (LN). To determine the effect of CXCL13 on SLE and explore the potential mechanisms, we tested serum concentrations of CXCL13 in patients and healthy individuals and found that CXCL13 expression was high in SLE patients especially in LN patients. When we treated human renal mesangial cells (HRMCs) in vitro with recombinant human CXCL13, the cell proliferation was accelerated, which was tested by Cell Counting Kit-8 assay and flow cytometry. Western blot and immunofluorescence assay revealed that CXCL13 would lead to phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2). However, the effect was weakened after the silence of CXCR5. The results of our study elaborated that high expression of CXCL13 could be involved in the pathogenesis of LN.
机译:作为趋化因子超家族的CXC亚型成员,CXCL13被认为与系统性红斑狼疮(SLE),特别是狼疮肾炎(LN)有关。为了确定CXCL13对SLE的作用并探讨其潜在机制,我们检测了患者和健康个体的血清CXCL13浓度,发现在SLE患者尤其是LN患者中CXCL13表达高。当我们用重组人CXCL13在体外处理人肾小球膜细胞(HRMC)时,细胞增殖得以加速,这通过Cell Counting Kit-8分析法和流式细胞仪进行了测试。免疫印迹和免疫荧光分析表明,CXCL13会导致细胞外信号调节激酶1/2(ERK1 / 2)磷酸化。但是,CXCR5沉默后,效果减弱了。我们的研究结果阐明,CXCL13的高表达可能与LN的发病机制有关。

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