Center for Host defense, Inflammation, and Lung Disease (CHILD) Research, Department of Pediatrics, The Pennsylvania State University College of Medicine, 500 University Drive, Hershey H085, PA 17033, USA.
Microb Pathog. 2012 Apr;52(4):239-49. doi: 10.1016/j.micpath.2012.01.005. Epub 2012 Jan 20.
Female mice exhibited higher survival rate than males after pneumonia, with a reversal of this pattern following ozone exposure. Surfactant protein A (SP-A) plays an important role in innate immunity and SP-A (-/-) mice were more susceptible to pneumonia than wild type mice. Here, we investigated underlying mechanisms of the differential susceptibility of mice to pneumonia. Wild type and SP-A (-/-) C57BL/6J male and female mice were exposed to ozone or filtered air (FA) and then infected intratracheally with Klebsiella pneumoniae. Blood, spleen, and lung were analyzed for bacterial counts, lung and spleen weights, and sex hormone and cortisol levels were measured in plasma within two days post-infection. We found: 1) in the absence of ozone-induced oxidative stress, males had higher level of bacterial dissemination compared to females; ozone exposure decreased pulmonary clearance in both sexes and ozone-exposed females were more affected than males; 2) ozone exposure increased lung weight, but decreased spleen weight in both sexes, and in both cases ozone-exposed females were affected the most; 3) plasma cortisol levels in infected mice changed: ozone-exposed>FA-exposed, females>males, and infected>non-infected; 4) no major sex hormone differences were observed in the studied conditions; 5) differences between wild type and SP-A (-/-) mice were observed in some of the studied conditions. We concluded that reduced pulmonary clearance, compromised spleen response to infection, and increased cortisol levels in ozone-exposed females, and the higher level of lung bacterial dissemination in FA-exposed males, contribute to the previously observed survival outcomes.
雌性小鼠在肺炎后比雄性小鼠的存活率更高,而在暴露于臭氧后,这种模式发生逆转。表面活性蛋白 A (SP-A) 在先天免疫中发挥重要作用,SP-A(-/-) 小鼠比野生型小鼠更容易患肺炎。在这里,我们研究了导致小鼠对肺炎易感性差异的潜在机制。将野生型和 SP-A(-/-) C57BL/6J 雄性和雌性小鼠暴露于臭氧或过滤空气 (FA) 中,然后经气管内感染肺炎克雷伯菌。在感染后两天内,分析血液、脾脏和肺中的细菌计数,测量肺和脾脏重量,以及血浆中的性激素和皮质醇水平。我们发现:1)在不存在臭氧诱导的氧化应激的情况下,雄性小鼠的细菌播散水平高于雌性小鼠;臭氧暴露降低了两性的肺部清除能力,臭氧暴露的雌性小鼠比雄性小鼠受影响更大;2)臭氧暴露增加了肺重量,但减少了两性的脾脏重量,并且臭氧暴露的雌性小鼠受影响最大;3)感染小鼠的血浆皮质醇水平发生变化:臭氧暴露>FA 暴露,雌性>雄性,感染>未感染;4)在研究条件下未观察到主要的性激素差异;5)在一些研究条件下观察到野生型和 SP-A(-/-) 小鼠之间的差异。我们得出结论,臭氧暴露雌性小鼠的肺部清除能力降低、脾脏对感染的反应受损以及皮质醇水平升高,以及 FA 暴露雄性小鼠的肺部细菌播散水平升高,导致了之前观察到的生存结果。