Dagenais André, Gosselin Diane, Guilbault Claudine, Radzioch Danuta, Berthiaume Yves
Centre de recherche, Centre hospitalier de l'Université de Montréal/ Hôtel-Dieu, Département de médecine, Université de Montréal, Montreal, Quebec, Canada.
Respir Res. 2005 Jan 6;6(1):2. doi: 10.1186/1465-9921-6-2.
The intratracheal instillation of Pseudomonas aeruginosa entrapped in agar beads in the mouse lung leads to chronic lung infection in susceptible mouse strains. As the infection generates a strong inflammatory response with some lung edema, we tested if it could modulate the expression of genes involved in lung liquid clearance, such as the alpha, beta and gamma subunits of the epithelial sodium channel (ENaC) and the catalytic subunit of Na+-K+-ATPase.
Pseudomonas aeruginosa entrapped in agar beads were instilled in the lung of resistant (BalB/c) and susceptible (DBA/2, C57BL/6 and A/J) mouse strains. The mRNA expression of ENaC and Na+-K+-ATPase subunits was tested in the lung by Northern blot following a 3 hours to 14 days infection.
The infection of the different mouse strains evoked regulation of alpha and beta ENaC mRNA. Following Pseudomonas instillation, the expression of alphaENaC mRNA decreased to a median of 43% on days 3 and 7 after infection and was still decreased to a median of 45% 14 days after infection (p < 0.05). The relative expression of betaENaC mRNA was transiently increased to a median of 241%, 24 h post-infection before decreasing to a median of 43% and 54% of control on days 3 and 7 post-infection (p < 0.05). No significant modulation of gammaENaC mRNA was detected although the general pattern of expression of the subunit was similar to alpha and beta subunits. No modulation of alpha1Na+-K+-ATPase mRNA, the catalytic subunit of the sodium pump, was recorded. The distinctive expression profiles of the three subunits were not different, between the susceptible and resistant mouse strains.
These results show that Pseudomonas infection, by modulating ENaC subunit expression, could influence edema formation and clearance in infected lungs.
在小鼠肺内气管内滴注包裹于琼脂珠中的铜绿假单胞菌会导致易感小鼠品系发生慢性肺部感染。由于该感染会引发强烈的炎症反应并伴有一定程度的肺水肿,我们测试了它是否能够调节参与肺液清除的基因表达,例如上皮钠通道(ENaC)的α、β和γ亚基以及Na⁺-K⁺-ATP酶的催化亚基。
将包裹于琼脂珠中的铜绿假单胞菌滴注到抗性(BalB/c)和易感(DBA/2、C57BL/6和A/J)小鼠品系的肺内。在感染3小时至14天后,通过Northern印迹法检测肺内ENaC和Na⁺-K⁺-ATP酶亚基的mRNA表达。
不同小鼠品系的感染引起了α和β ENaC mRNA的调节。滴注铜绿假单胞菌后,感染后第3天和第7天,αENaC mRNA的表达降至中位数的43%,感染后14天仍降至中位数的45%(p<0.05)。βENaC mRNA的相对表达在感染后24小时短暂增加至中位数的241%,然后在感染后第3天和第7天降至对照组中位数的43%和54%(p<0.05)。尽管γENaC亚基的总体表达模式与α和β亚基相似,但未检测到γENaC mRNA的显著调节。未记录到钠泵催化亚基α1Na⁺-K⁺-ATP酶mRNA的调节。在易感和抗性小鼠品系之间,这三个亚基的独特表达谱没有差异。
这些结果表明,铜绿假单胞菌感染通过调节ENaC亚基表达,可能影响感染肺内的水肿形成和清除。