Department of Biomedical Science, Bond University, Queensland, Australia.
J Urol. 2012 Mar;187(3):1087-93. doi: 10.1016/j.juro.2011.10.129. Epub 2012 Jan 21.
We determined the effects of Pseudomonas aeruginosa virulence factor pyocyanin on human urothelial cell viability and function in vitro.
RT4 urothelial cells were treated with pyocyanin (1 to 100 μM) for 24 hours. After exposure the treatment effects were measured according to certain end points, including changes in urothelial cell viability, reactive oxygen species formation, caspase-3 activity, basal and stimulated adenosine triphosphate release, SA-β-gal activity and detection of acidic vesicular organelles.
The 24-hour pyocyanin treatment resulted in a concentration dependent decrease in cell viability at concentrations of 25 μM or greater, and increases in reactive oxygen species formation and caspase-3 activity at 25 μM or greater. Basal adenosine triphosphate release was significantly decreased at all tested pyocyanin concentrations while stimulated adenosine triphosphate release was significantly inhibited at pyocyanin concentrations of 12.5 μM or greater with no significant stimulated release at 100 μM. Pyocyanin treated RT4 cells showed morphological characteristics associated with cellular senescence, including SA-β-gal expression. This effect was not evident at 100 μM pyocyanin and may have been due to apoptotic cell death, as indicated by increased caspase-3 activity. An increase in acridine orange stained vesicular-like organelles was observed in RT4 urothelial cells after pyocyanin treatment.
Exposure to pyocyanin alters urothelial cell viability, reactive oxygen species production and caspase-3 activity. Treatment also results in cellular senescence, which may affect the ability of urothelium to repair during infection. The virulence factor depressed stimulated adenosine triphosphate release, which to our knowledge is a novel finding with implications for awareness of bladder filling in patients with P. aeruginosa urinary tract infection.
本研究旨在探讨铜绿假单胞菌毒力因子绿脓菌素对人尿路上皮细胞活力和功能的体外影响。
将 RT4 尿路上皮细胞用绿脓菌素(1 至 100μM)处理 24 小时。暴露后,根据某些终点测量治疗效果,包括尿路上皮细胞活力变化、活性氧物质形成、半胱天冬酶-3 活性、基础和刺激三磷酸腺苷释放、SA-β-半乳糖苷活性和酸性囊泡细胞器检测。
24 小时绿脓菌素处理导致细胞活力在 25μM 或更高浓度时呈浓度依赖性下降,在 25μM 或更高浓度时活性氧物质形成和半胱天冬酶-3 活性增加。基础三磷酸腺苷释放显著减少,在所有测试的绿脓菌素浓度下,刺激三磷酸腺苷释放在 12.5μM 或更高浓度时显著抑制,在 100μM 时无显著刺激释放。绿脓菌素处理的 RT4 细胞显示与细胞衰老相关的形态学特征,包括 SA-β-半乳糖苷表达。在 100μM 绿脓菌素时未见此作用,可能是由于细胞凋亡,如半胱天冬酶-3 活性增加所示。在用绿脓菌素处理后,在 RT4 尿路上皮细胞中观察到吖啶橙染色的囊泡样细胞器增加。
暴露于绿脓菌素会改变尿路上皮细胞活力、活性氧物质产生和半胱天冬酶-3 活性。治疗还导致细胞衰老,这可能会影响感染期间尿路上皮修复的能力。该毒力因子抑制刺激三磷酸腺苷释放,据我们所知,这是一个新的发现,对了解铜绿假单胞菌尿路感染患者的膀胱充盈有意义。