首页> 外文期刊>American Journal of Physiology >Bladder urothelial BK channel activity is a critical mediator for innate immune response in urinary tract infection pathogenesis
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Bladder urothelial BK channel activity is a critical mediator for innate immune response in urinary tract infection pathogenesis

机译:膀胱尿路上皮BK通道活性是尿路感染发病机制中先天免疫反应的关键介质

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摘要

Inflammatory biomarkers (chemokines and cytokines) were measured in urine specimens collected 2 h after inoculation using a 32-multiplex ELISA. Of these 32 biomarkers, 19 and 15 were significantly elevated 2 h after LPS and UPEC exposure, respectively. IBTX significantly abrogated the elevations of 15 out of 19 biomarkers after LPS inoculation and 12 out of 15 biomarkers after UPEC inoculation. In a separate experiment, qPCR for IL-6, interfer-on-7-induced protein 10 (CXCL10), and macrophage inflammatory protein 2 (CXCL2) in urothelium paralleled the changes measured in urine of these same biomarkers, supporting that urinary changes in biomarker levels reflected urothelial expression changes. These in vivo data demonstrated that BK channel activity is crucial in the urothelial host innate immune response, as measured by changes in urinary biomarkers, in UTI pathogenesis.
机译:使用 32 多重 ELISA 在接种后 2 小时收集的尿液标本中测量炎症生物标志物(趋化因子和细胞因子)。在这 32 种生物标志物中,19 种和 15 种分别在 LPS 和 UPEC 暴露后 2 小时显着升高。IBTX显著消除了LPS接种后19个生物标志物中的15个和UPEC接种后15个生物标志物中的12个升高。在另一项实验中,尿路上皮细胞中 IL-6、干扰蛋白 7 诱导蛋白 10 (CXCL10) 和巨噬细胞炎症蛋白 2 (CXCL2) 的 qPCR 与这些相同生物标志物在尿液中测量的变化平行,支持尿液生物标志物水平的变化反映了尿路上皮表达的变化。这些体内数据表明,BK通道活性在尿路上皮宿主先天免疫反应中至关重要,这是通过尿液生物标志物的变化来衡量的,在UTI发病机制中。

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