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The Effect of miR-146a on the Gene Expression of Immunoregulatory Cytokines in Human Mesenchymal Stromal Cells

机译:miR-146a对人间充质基质细胞中免疫调节细胞因子的基因表达的影响

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摘要

Mounting evidence indicates that microRNAs (miRNAs), including miR-146a, have an impact on the immunomodulatory activities of mesenchymal stem/stromal cells (MSCs). Suppression of inflammatory macrophage activation is one of the main immunomodulatory mechanisms of MSCs. Here, we investigated whether miR-146a in MSCs might play a role in the effects of MSCs on macrophage activation. A miRNA microarray revealed that miR-146a was the most highly upregulated miRNA in MSCs upon co-culture with activated macrophages. Inhibition of miR-146a in MSCs through miR-146a inhibitor transfection had a different effect on the expression of immunoregulatory factors secreted by MSCs. Pentraxin 3, tumor necrosis factor-inducible gene 6, and cyclooxygenase-2, which are well-known mediators of the immunomodulatory functions of MSCs, were significantly upregulated in MSCs after miR-146a knockdown. By contrast, hepatocyte growth factor and stanniocalcin 1, other immunoregulatory molecules expressed by MSCs, were downregulated by miR-146a knockdown. Consequently, the inhibition of miR-146a in MSCs did not change the overall effect of MSCs on the suppression of inflammatory macrophage activation or the induction of anti-inflammatory macrophage polarization.
机译:安装证据表明MicroRNA(miRNA),包括miR-146a,对间充质茎/基质细胞(MSC)的免疫调节活性产生影响。抑制炎症巨噬细胞活化是MSCs的主要免疫调节机制之一。在这里,我们调查了MSCS中的miR-146a是否可能在MSCS对巨噬细胞激活的影响中发挥作用。 miRNA微阵列显示MiR-146a在具有活化巨噬细胞的共同培养上是MSCs中最高度上调的miRNA。通过MIR-146A抑制剂转染在MSC上的miR-146a对MIR-146a的抑制对MSCs分泌的免疫导致因子的表达产生了不同的影响。在MIR-146A敲低后,在MSCs之后,在MSCs中显着上调,肿瘤坏死因子诱导基因6和环氧氧酶-2是MSCs的免疫调节功能的鉴别介质。相比之下,肝细胞生长因子和锡烷酰亚胺1,MSCs表达的其他免疫调节分子通过miR-146a敲低来调整。因此,MIR-146A在MSCs中的抑制性并未改变MSCs对抑制炎症巨噬细胞活化或抗炎巨噬细胞极化诱导的整体效果。

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