Kunzelmann Karl, Scheidt Kerstin, Scharf Birgit, Ousingsawat Jiraporn, Schreiber Rainer, Wainwright Brandon, McMorran Brendan
Institut für Physiologie, Universität Regensburg, Regensburg, Germany.
FASEB J. 2006 Mar;20(3):545-6. doi: 10.1096/fj.05-4454fje. Epub 2006 Jan 12.
Pseudomonas aeruginosa causes severe life-threatening airway infections that are a frequent cause for hospitalization of cystic fibrosis (CF) patients. These Gram-negative pathogens possess flagella that contain the protein flagellin as a major structural component. Flagellin binds to the host cell glycolipid asialoGM1 (ASGM1), which appears enriched in luminal membranes of respiratory epithelial cells. We demonstrate that in mouse airways, luminal exposure to flagellin leads to inhibition of Na+ absorption by the epithelial Na+ channel ENaC, but does not directly induce a secretory response. Inhibition of ENaC was observed in tracheas of wild-type mice and was attenuated in mice homozygous for the frequent cystic fibrosis conductance regulator (CFTR) mutation G551D. Similar to flagellin, anti-ASGM1 antibody also inhibited ENaC. The inhibitory effects of flagellin on ENaC were attenuated by blockers of the purinergic signaling pathway, although an increase in the intracellular Ca2+ concentration by recombinant or purified flagellin or whole flagella was not observed. Because an inhibitor of the mitogen-activated protein kinase (MAPK) pathway also attenuated the effects of flagellin on Na+ absorption, we conclude that flagellin exclusively inhibits ENaC, probably due to release of ATP and activation of purinergic receptors of the P2Y subtype. Stimulation of these receptors activates the MAPK pathway, thereby leading to inhibition of ENaC. Thus, P. aeruginosa reduces Na+ absorption, which could enhance local mucociliary clearance, a mechanism that seem to be attenuated in CF.
铜绿假单胞菌可引发严重的、危及生命的气道感染,这是囊性纤维化(CF)患者频繁住院的常见原因。这些革兰氏阴性病原体具有鞭毛,鞭毛含有鞭毛蛋白作为主要结构成分。鞭毛蛋白与宿主细胞糖脂脱唾液酸神经节苷脂(ASGM1)结合,ASGM1似乎在呼吸道上皮细胞的腔膜中富集。我们证明,在小鼠气道中,腔内暴露于鞭毛蛋白会导致上皮钠通道ENaC对Na+吸收的抑制,但不会直接诱导分泌反应。在野生型小鼠的气管中观察到ENaC受到抑制,而在频繁出现囊性纤维化跨膜传导调节因子(CFTR)突变G551D的纯合小鼠中,这种抑制作用减弱。与鞭毛蛋白类似,抗ASGM1抗体也能抑制ENaC。尽管未观察到重组或纯化的鞭毛蛋白或完整鞭毛使细胞内Ca2+浓度升高,但嘌呤能信号通路的阻滞剂可减弱鞭毛蛋白对ENaC的抑制作用。由于丝裂原活化蛋白激酶(MAPK)通路的抑制剂也减弱了鞭毛蛋白对Na+吸收的影响,我们得出结论,鞭毛蛋白专门抑制ENaC,可能是由于ATP的释放和P2Y亚型嘌呤能受体的激活。这些受体的刺激激活了MAPK通路,从而导致ENaC受到抑制。因此,铜绿假单胞菌会减少Na+吸收,这可能会增强局部黏液纤毛清除功能,而在CF中这种机制似乎会减弱。