白介素-8受体(CXCR1和CXCR2)在绝经前复发性尿路感染妇女中的表达

Alex Smithson, Maria Rosa Sarrias, Juanjo Barcelo, Belen Suarez, Juan Pablo Horcajada, Sara Maria Soto, Alex Soriano, Jordi Vila, Jose Antonio Martinez, Jordi Vives, Jose Mensa, Francisco Lozano
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引用次数: 43

摘要

中性粒细胞通过感染组织的迁移是由CXC趋化因子及其受体(CXCR1和CXCR2)介导的。已经提出CXCR1缺乏可能导致儿童急性肾盂肾炎的易感性。本研究的目的是评估绝经前复发性尿路感染妇女中CXCR1和CXCR2的表面表达以及CXCR1基因多态性的存在。该研究包括20名患有复发性尿路感染、尿路正常、没有可能与复发性尿路感染相关疾病的绝经前妇女,以及30名没有既往尿路感染的对照组。流式细胞术通过测量平均荧光强度(MFI)通道检测和分析CXCR1和CXCR2在中性粒细胞上的表达水平。利用序列分型方法分析了CXCR1基因的启动子和编码区是否存在多态性。根据MFI值,复发性尿路感染患者表现出CXCR1表达的中位数水平,与对照组相似。CXCR2分析显示,复发性尿路感染患者的MFI值中位表达水平低于对照组(P = 0.002, Mann-Whitney U检验)。在患者或对照组中,在CXCR1基因的启动子或外显子1区域未检测到多态性。在CXCR1的外显子2处检测到多态性,但其频率在患者和对照组之间没有差异。我们发现复发性尿路感染患者中CXCR2表达水平较低。这些结果提示,低水平的CXCR2表达可能会增加绝经前妇女对尿路感染的易感性。
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Expression of interleukin-8 receptors (CXCR1 and CXCR2) in premenopausal women with recurrent urinary tract infections.

The migration of neutrophils through infected tissues is mediated by the CXC chemokines and its receptors (CXCR1 and CXCR2). It has been proposed that a CXCR1 deficiency could confer susceptibility to acute pyelonephritis in children. The objective of the study is to assess the surface expression of CXCR1 and CXCR2 and the existence of polymorphisms in the CXCR1 gene in premenopausal women with recurrent urinary tract infections. The study included 20 premenopausal women with recurrent urinary infections, with normal urinary tracts, and without diseases potentially associated with relapsing urinary infections and 30 controls without previous urinary infections. The levels of CXCR1 and CXCR2 expression on neutrophils were measured and analyzed by flow cytometry by measuring the mean fluorescence intensity (MFI) channel. The promoter and coding regions of the CXCR1 gene were analyzed for the presence of polymorphisms by a sequence-based typing method. Patients with recurrent urinary tract infections exhibited median levels of CXCR1 expression, determined from MFI values, similar to those of the controls. The analysis of CXCR2 showed that patients with recurrent urinary infections had lower median levels of expression, determined from the MFI values, than the controls (P = 0.002, Mann-Whitney U test). No polymorphisms were detected at the promoter or at the exon 1 region of the CXCR1 gene either in the patients or in the controls. Polymorphisms were detected at the exon 2 of CXCR1, but their frequencies did not differ between patients and controls. We have found a low level of CXCR2 expression in patients with recurrent urinary tract infections. These results suggest that a low level of CXCR2 expression may increase the susceptibilities of premenopausal women to urinary tract infections.

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