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TOP NEPHROLOGY/UROLOGY PAPERS FROM 2012

机译:从2012年开始肾脏肾脏/泌尿外科论文

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The urinary bladder is a common site of bacterial infection with a majority of cases attributed to uropathogenic Escherichia coli. Sequelae of urinary tract infections (UTIs) include the loss of urothelial barrier function and subsequent clinical morbidity secondary to the permeation of urine potassium, urea and ammonia into the subepithelium. To date there has been limited research describing the mechanism by which this urothelial permeability defect develops. The present study models acute uropathogenic E. coli infection in vitro using intact canine bladder mucosa mounted in Ussing chambers to determine whether infection induces primarily a transcellular or paracellular permeability defect. The Ussing chamber sustains tissue viability while physically separating submucosal and lumen influences, so this model is ideal for quantitative measurement of transepithelial electrical resistance (TER) to assess alterations of urothelial barrier function. Using this model, changes in both tissue ultrastructure and TER indicated that uropathogenic E. coli infection promotes a paracellular permeability defect associated with the failure of umbrella cell tight junction formation and umbrella cell sloughing. In addition, bacterial interaction with the urothelium promoted secretion of cytokines from the urinary bladder with bioactivity capable of modulating epithelial barrier function including tumour necrosis factor-a, interleukin (IL)-6 and IL-15. IL-15 secretion by the infected bladder mucosa is a novel finding and, because IL-15 plays key roles in reconstitution of tight junction function in damaged intestine, this study points to a potential role for IL-15 in UTI-induced urothelial injury.
机译:膀胱是细菌感染的常见位点,大多数患者归因于尿羟疗法大肠杆菌。尿路感染(UTI)的后遗症包括尿液阻隔功能的丧失和继发于尿液,尿素和氨的渗透到脑膜炎中的临床发病率。迄今为止,研究了该机制的有限研究,该机制是这种尿道渗透性缺陷的发展。本研究模型使用安装在USSing腔室中的完整犬膀胱粘膜体外急性尿胆肠病大肠杆菌感染,以确定感染是否主要是透析细胞或肺细胞渗透性缺陷。 USSing腔室在物理分离粘膜和腔的影响时维持组织活力,因此该模型是定量测量Transepithelial电阻(TER)以评估尿液阻挡功能的改变。使用该模型,两种组织超微结构和TER的变化表明尿羟致致疗法大肠杆菌感染促进与伞形细胞密封接线形成和伞形细胞脱落的失效相关的肺细胞渗透性缺陷。此外,与尿液中的细菌相互作用促进了从膀胱分泌细胞因子,其生物活性能够调节上皮阻隔功能,包括肿瘤坏死因子-A,白细胞介素(IL)-6和IL-15。 IL-15受感染的膀胱粘膜的分泌是一种新的发现,因为IL-15在受损的肠道重构紧密结函数中起关键作用,本研究指出了IL-15在UTI诱导的尿液损伤中的潜在作用。

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