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促红细胞生成素类似物ARA290调节天然免疫反应并减少大肠杆菌对尿道上皮细胞的侵袭。

The erythropoietin analogue ARA290 modulates the innate immune response and reduces Escherichia coli invasion into urothelial cells.

作者信息

Polgárová Kamila, Lüthje Petra, Cerami Anthony, Brauner Annelie

机构信息

Department of Microbiology, Tumor and Cell biology, Clinical Microbiology, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

出版信息

FEMS Immunol Med Microbiol. 2011 Jul;62(2):190-6. doi: 10.1111/j.1574-695X.2011.00801.x. Epub 2011 Apr 11.

Abstract

Urinary tract infections (UTI) are one of the most common infectious diseases worldwide. The majority is caused by uropathogenic Escherichia coli. Emerging resistances against conventional antimicrobial therapy requires novel treatment strategies. Beside its role in erythropoiesis, erythropoietin has been recognized to exert tissue-protective and immunomodulatory properties. Here, we investigated the nonerythropoietic erythropoietin analogue ARA290 for potential properties to modulate uroepithelial infection by E. coli in a cell culture model. Expression of the erythropoietin receptor was increased by bacterial stimuli and further enhanced by ARA290 in bladder epithelial cell lines and primary cells as well as in the monocytic cell line THP-1. Stimulation with ARA290 promoted an immune response, inducing a strong initial, but temporarily limited interleukin-8 induction. Moreover, the invasion of bladder epithelial cells by E. coli was significantly reduced in cells costimulated with ARA290. Our results indicate that the erythropoietin analogue ARA290 might be a candidate for the development of novel treatment strategies against UTI, by boosting an early immune response and reducing bacterial invasion as a putative source for recurrent infections.

摘要

尿路感染(UTI)是全球最常见的传染病之一。大多数尿路感染是由尿路致病性大肠杆菌引起的。对传统抗菌治疗出现的耐药性需要新的治疗策略。除了在红细胞生成中的作用外,促红细胞生成素还具有组织保护和免疫调节特性。在此,我们在细胞培养模型中研究了非促红细胞生成素类似物ARA290调节大肠杆菌对尿路上皮感染的潜在特性。在膀胱上皮细胞系、原代细胞以及单核细胞系THP-1中,细菌刺激可增加促红细胞生成素受体的表达,而ARA290可进一步增强其表达。用ARA290刺激可促进免疫反应,诱导强烈的初始但暂时有限的白细胞介素-8诱导。此外,在与ARA290共刺激的细胞中,大肠杆菌对膀胱上皮细胞的侵袭显著减少。我们的结果表明,促红细胞生成素类似物ARA290可能是开发新型UTI治疗策略的候选药物,通过增强早期免疫反应和减少作为复发性感染假定来源的细菌侵袭来实现。

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