Pulmonary Research Group, Department of Medicine, University of Alberta, 550 Heritage Medical Research Center, Edmonton, Alberta, Canada.
Pflugers Arch. 2012 Mar;463(3):497-509. doi: 10.1007/s00424-011-1064-9. Epub 2011 Dec 15.
Protease-activated receptor 2 (PAR-2) is a G protein-coupled receptor possibly involved in the pathogenesis of asthma. PAR-2 also modulates ion transport in cultured epithelial cells, but these effects in native airways are controversial. The influence of allergic inflammation on PAR-2-induced changes in ion transport has received little attention. Here, we studied immediate changes in transepithelial short circuit current (I (sc)) induced by PAR-2 activation in the tracheas of naive and allergic mice. Activation of PAR-2 with an apically added activation peptide (AP) induced a small increase in I (sc), while a much larger increase was observed following basolateral AP addition. In ovalbumin-sensitized and -challenged animals used as a model of allergic airway inflammation, the effect of basolateral AP addition was enhanced. Responses to basolateral AP in both naive and allergic mice were not decreased by blocking sodium absorption with amiloride or CFTR function with CFTR(inh)172 but were reduced by the cyclooxygenase inhibitor indomethacin and largely blocked (>80%) by niflumic acid, a calcium-activated chloride channels' (CaCC) blocker. Allergic mice also showed an enhanced response to ATP and thapsigargin. There was no change in mRNA expression of Par-2 or of the chloride channels Ano1 (Tmem16a) and Bestrophin 2 in tracheas from allergic mice, while mRNA levels of Bestrophin 1 were increased. In conclusion, basolateral PAR-2 activation in the mouse airways led to increased anion secretion through apical CaCC, which was more pronounced in allergic animals. This could be a protective mechanism aimed at clearing allergens and defending against mucus plugging.
蛋白酶激活受体 2(PAR-2)是一种 G 蛋白偶联受体,可能参与哮喘的发病机制。PAR-2 还调节培养的上皮细胞中的离子转运,但这些在天然气道中的作用存在争议。过敏炎症对 PAR-2 诱导的离子转运变化的影响受到的关注较少。在这里,我们研究了 PAR-2 激活在过敏和非过敏小鼠气管中引起的跨上皮短路电流(I(sc))的即时变化。用上皮顶端添加的激活肽(AP)激活 PAR-2 会引起 I(sc)的小幅度增加,而在基底外侧 AP 加入后观察到更大的增加。在卵清蛋白致敏和激发的动物中,作为过敏气道炎症的模型,基底外侧 AP 加入的作用增强。基底外侧 AP 的反应在过敏和非过敏小鼠中均未因用阿米洛利阻断钠吸收或用 CFTR(inh)172 阻断 CFTR 功能而降低,但被环氧化酶抑制剂吲哚美辛和钙激活氯离子通道(CaCC)阻断剂尼氟灭酸降低,并且>80%被尼氟灭酸阻断。过敏小鼠对 ATP 和他普西龙的反应也增强。过敏小鼠气管中 Par-2 或氯离子通道 Ano1(Tmem16a)和 Bestrophin 2 的 mRNA 表达没有变化,而 Bestrophin 1 的 mRNA 水平增加。总之,在小鼠气道中基底外侧 PAR-2 的激活导致通过顶端 CaCC 增加阴离子分泌,在过敏动物中更为明显。这可能是一种旨在清除过敏原和防止粘液堵塞的保护机制。