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阴道毛滴虫通过活性氧和钾离子外流激活NLRP3炎性小体,从而在人前列腺上皮细胞系中诱导白细胞介素-1β的产生。

Trichomonas vaginalis induces IL-1β production in a human prostate epithelial cell line by activating the NLRP3 inflammasome via reactive oxygen species and potassium ion efflux.

作者信息

Gu Na-Yeong, Kim Jung-Hyun, Han Ik-Hwan, Im Su-Jeong, Seo Min-Young, Chung Yong-Hoon, Ryu Jae-Sook

机构信息

Department of Environmental Biology and Medical Parasitology, Hanyang University College of Medicine, Hanyang University, Seoul, Korea.

Department of Biomedical Science, Graduate School of Biomedical Science and Engineering, Hanyang University, Seoul, Korea.

出版信息

Prostate. 2016 Jul;76(10):885-96. doi: 10.1002/pros.23178. Epub 2016 Mar 9.

Abstract

BACKGROUND

Trichomonas vaginalis is a sexually transmitted protozoan parasite that causes vaginitis in women, and urethritis and prostatitis in men. IL-1β is synthesized as immature pro-IL-1β, which is cleaved by activated caspase-1. Caspase-1 is, in turn, activated by a multi-protein complex known as an inflammasome. In this study, we investigated the inflammatory response of a prostate epithelial cell line (RWPE-1) to T. vaginalis and, specifically, the capacity of T. vaginalis to activate the NLRP3 inflammasome.

METHODS

RWPE-1 cells were stimulated by live T. vaginalis, and subsequent expression of pro-IL-1β, IL-1β, NLRP3, ASC and caspase-1 was determined by real-time PCR and Western blotting. IL-1β and caspase-1 production was also measured by ELISA. To evaluate the effects of NLRP3 and caspase-1 on IL-1β production, the activated RWPE-1 cells were transfected with small interfering RNAs to silence the NLRP3 and caspase-1 genes. Activation of the NLRP3 inflammasome was observed by fluorescence microscopy. Intracellular reactive oxygen species (ROS) were evaluated by spectrofluorometry.

RESULTS

When RWPE-1 cells were stimulated with live T. vaginalis, the mRNA and protein expression of IL-1β, NLRP3, ASC, and caspase-1 increased. Moreover, silencing of NLRP3 and caspase-1 attenuated T. vaginalis-induced IL-1β secretion. The NADPH oxidase inhibitor DPI and high extracellular potassium ion suppressed the production of IL-1β, caspase-1, and the expression of NLRP3 and ASC proteins. The specific NF-κB inhibitor, Bay 11-7082, inhibited IL-1β production, and also inhibited the production of caspase-1, ASC and NLRP3 proteins.

CONCLUSIONS

T. vaginalis induces the formation of the NLRP3 inflammasome in human prostate epithelial cells via ROS and potassium ion efflux, and this results in IL-1β production. This is the first evidence for activation of the NLRP3 inflammasome in the inflammatory response by prostate epithelial cells infected with T. vaginalis. Prostate 76:885-896, 2016. © 2016 Wiley Periodicals, Inc.

摘要

背景

阴道毛滴虫是一种性传播原生动物寄生虫,可导致女性阴道炎以及男性尿道炎和前列腺炎。白细胞介素-1β(IL-1β)最初以未成熟的前体形式合成,随后被活化的半胱天冬酶-1切割。半胱天冬酶-1反过来又被一种称为炎性小体的多蛋白复合物激活。在本研究中,我们调查了前列腺上皮细胞系(RWPE-1)对阴道毛滴虫的炎症反应,特别是阴道毛滴虫激活NLRP3炎性小体的能力。

方法

用活的阴道毛滴虫刺激RWPE-1细胞,随后通过实时聚合酶链反应(PCR)和蛋白质免疫印迹法检测前体IL-1β、IL-1β、NLRP3、凋亡相关斑点样蛋白(ASC)和半胱天冬酶-1的表达。还通过酶联免疫吸附测定(ELISA)检测IL-1β和半胱天冬酶-1的产生。为了评估NLRP3和半胱天冬酶-1对IL-1β产生的影响,将活化的RWPE-1细胞用小干扰RNA转染以沉默NLRP3和半胱天冬酶-1基因。通过荧光显微镜观察NLRP3炎性小体的激活情况。通过荧光分光光度法评估细胞内活性氧(ROS)。

结果

当用活的阴道毛滴虫刺激RWPE-1细胞时,IL-1β、NLRP3、ASC和半胱天冬酶-1的信使核糖核酸(mRNA)和蛋白质表达增加。此外,沉默NLRP3和半胱天冬酶-1可减弱阴道毛滴虫诱导的IL-1β分泌。烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶抑制剂二苯基碘鎓(DPI)和高细胞外钾离子抑制IL-1β、半胱天冬酶-1的产生以及NLRP3和ASC蛋白的表达。特异性核因子κB(NF-κB)抑制剂Bay 11-7082抑制IL-1β的产生,同时也抑制半胱天冬酶-1、ASC和NLRP3蛋白的产生。

结论

阴道毛滴虫通过ROS和钾离子外流诱导人前列腺上皮细胞中NLRP3炎性小体的形成,进而导致IL-1β的产生。这是感染阴道毛滴虫的前列腺上皮细胞在炎症反应中激活NLRP3炎性小体的首个证据。《前列腺》76:885 - 896,2016年。©2016威利期刊公司

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