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TSG-6和uroplakin III在大鼠和人类膀胱疼痛综合征/间质性膀胱炎中的作用。

The role of TSG-6 and uroplakin III in bladder pain syndrome/ interstitial cystitis in rats and humans.

作者信息

Lv Yi-Song, Gao Rui, Lin Qing-Ming, Jiang Tao, Chen Qin, Tang Song-Xi, Mao Hou-Ping, Zhou Hui-Liang, Cao Lin-Sheng

机构信息

Department of Urology, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, China.

Department of Emergency Medicine, Fujian Provincial Hospital, Fuzhou 350005, China.

出版信息

Iran J Basic Med Sci. 2017 Nov;20(11):1242-1249. doi: 10.22038/IJBMS.2017.9540.

Abstract

OBJECTIVES

We investigated the relationship between the expression of tumor necrosis factor-inducible gene 6 (TSG-6) with inflammation and integrity of the bladder epithelium in the bladder tissues of patients with bladder pain syndrome/interstitial cystitis (BPS/IC) and the mechanism of action using a rat model of BPS/IC.

MATERIALS AND METHODS

Expression of TSG-6 and uroplakin III was determined by immuno- histochemistry of bladder biopsy samples from control human subjects and patients with verified BPS/IC. Our rat model of BPS/IC was employed to measure the perfusion of bladders with hyaluronidase, and assessment of the effect of TSG-6 administration on disease progression. Treatment effects were assessed by measurement of metabolic characteristics, RT-PCR of TGR-6 and interleukin-6, bladder histomorphology, and immunohistochemistry of TGR-6 and uroplakin III.

RESULTS

The bladders of patients with BPS/IC had lower expression of uroplakin III and higher expression of TSG-6 than controls. Rats treated with hyaluronidase for 1 week developed the typical signs and symptoms of BPS/IC, and rats treated with hyaluronidase for 4 weeks had more serious disease. Administration of TSG-6 reversed the effects of hyaluronidase and protected against disease progression.

CONCLUSION

Our results indicate that TSG-6 plays an important role in maintaining the integrity of the bladder epithelial barrier.

摘要

目的

我们研究了膀胱疼痛综合征/间质性膀胱炎(BPS/IC)患者膀胱组织中肿瘤坏死因子诱导基因6(TSG-6)的表达与炎症及膀胱上皮完整性之间的关系,并使用BPS/IC大鼠模型探讨其作用机制。

材料与方法

通过对健康对照者和确诊为BPS/IC患者的膀胱活检样本进行免疫组织化学检测,测定TSG-6和尿路上皮蛋白III的表达。利用我们建立的BPS/IC大鼠模型,测量膀胱透明质酸酶灌注情况,并评估TSG-6给药对疾病进展的影响。通过测量代谢特征、TSG-6和白细胞介素-6的逆转录聚合酶链反应(RT-PCR)、膀胱组织形态学以及TSG-6和尿路上皮蛋白III的免疫组织化学来评估治疗效果。

结果

与对照组相比,BPS/IC患者膀胱中尿路上皮蛋白III的表达较低,而TSG-6的表达较高。用透明质酸酶处理1周的大鼠出现了BPS/IC的典型体征和症状,用透明质酸酶处理4周的大鼠病情更严重。给予TSG-6可逆转透明质酸酶的作用并预防疾病进展。

结论

我们的结果表明,TSG-6在维持膀胱上皮屏障的完整性方面发挥着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c35/5749359/d9e06cd6c1ab/IJBMS-20-1242-g001.jpg

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