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NLRP3和NLRC4炎性小体在致病性尿路感染中的作用

Involvement of NLRP3 and NLRC4 Inflammasome in Uropathogenic Mediated Urinary Tract Infections.

作者信息

Verma Vivek, Gupta Surbhi, Kumar Parveen, Yadav Sonal, Dhanda Rakesh Singh, Gaind Rajni, Arora Renu, Frimodt-Møller Niels, Yadav Manisha

机构信息

Dr. B.R. Ambedkar Center for Biomedical Research, University of Delhi, New Delhi, India.

Department of Urology, University of Alabama at Birmingham, Birmingham, AL, United States.

出版信息

Front Microbiol. 2019 Sep 3;10:2020. doi: 10.3389/fmicb.2019.02020. eCollection 2019.

Abstract

BACKGROUND

Inflammatory response during urinary tract infection (UTI) is mediated by innate immune defense. Nod like receptors (NLRs) have been proposed to work simultaneously beside TLR pathways to mediate pro-inflammatory response and maintain tissue homeostasis. Some reports have showed the involvement of inflammasome during uropathogenic (UPEC) mediated UTI. So we have sought to determine the status of various inflammasomes and their components in UPEC mediated UTI.

METHODS

A total of 186 females experiencing the first episode of UTI were recruited for the study and forty were found to be positive for UPEC (≥10 CFU/ml) in their urine ( = 40). Further, we analyzed the expression of , , , , , , and gene at mRNA and protein level in the blood of UPEC confirmed study subjects through real time qPCR and immunoblotting. Healthy females ( = 40) visiting the OPD for health checkups, family planning advice and subjects undergoing routine medical examinations, were recruited as healthy control subjects. Pro-inflammatory cytokines (IL-6, IL-8, IFN-γ, TNF-α and MCP-1) were measured in the plasma of patients and controls through ELISA. For investigation of the involvement of and inflammasome, studies were performed using co-immunoprecipitation and confocal microscopy.

RESULTS

Most of the inflammatory regulators studied (i.e., , and ) were found to be up-regulated at both mRNA and protein levels in the UPEC infected UTI patients. Also, pro-inflammatory cytokines (IL-6, IL-8, IFN-γ, TNF-α, and MCP-1) were found to be up-regulated in the patients group. However, no significant difference was observed in the expression of and genes at both mRNA and protein levels. Further, studies have shown the involvement of NLRC4 inflammasome in UPEC infected THP1 derived macrophages.

CONCLUSION

Involvement of and inflammasomes in UPEC infected UTI is evident from our findings. This is the first report showing levels of inflammasome and its components in UTI patients suggesting a possible role during UPEC mediated UTI. We have also reported the involvement of inflammasome for the first time during UTI infection.

摘要

背景

尿路感染(UTI)期间的炎症反应由先天免疫防御介导。有人提出核苷酸结合寡聚化结构域样受体(NLRs)在Toll样受体(TLR)途径之外协同发挥作用,以介导促炎反应并维持组织稳态。一些报告显示炎症小体在尿路致病性大肠杆菌(UPEC)介导的UTI中发挥作用。因此,我们试图确定各种炎症小体及其成分在UPEC介导的UTI中的状态。

方法

总共招募了186名首次发生UTI的女性参与该研究,其中40名女性尿液中UPEC检测呈阳性(≥10 CFU/ml)(n = 40)。此外,我们通过实时定量聚合酶链反应(qPCR)和免疫印迹分析了UPEC确诊研究对象血液中NLRP1、NLRP3、NLRC4、ASC、CASP1、IL-1β和IL-18基因在mRNA和蛋白质水平的表达。招募到门诊进行健康检查、计划生育咨询的健康女性(n = 40)以及接受常规体检的对象作为健康对照。通过酶联免疫吸附测定(ELISA)检测患者和对照血浆中的促炎细胞因子(IL-6、IL-8、IFN-γ、TNF-α和MCP-1)。为了研究NLRP3和NLRC4炎症小体的作用,使用免疫共沉淀和共聚焦显微镜进行了研究。

结果

在UPEC感染的UTI患者中,大多数研究的炎症调节因子(即NLRP1、NLRP3和NLRC4)在mRNA和蛋白质水平均上调。此外,患者组中促炎细胞因子(IL-6、IL-8、IFN-γ、TNF-α和MCP-1)也上调。然而,NLRP2和NLRP6基因在mRNA和蛋白质水平的表达未观察到显著差异。此外,研究表明NLRC4炎症小体参与UPEC感染的THP1衍生巨噬细胞。

结论

我们的研究结果表明NLRP3和NLRC4炎症小体参与UPEC感染的UTI。这是第一份显示UTI患者炎症小体及其成分水平的报告,表明其在UPEC介导的UTI中可能发挥作用。我们还首次报告了NLRP1炎症小体在UTI感染中的作用。

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