首页> 美国卫生研究院文献>The Journal of General Physiology >Soluble Mediators Not Cilia Determine Airway Surface Liquid Volume in Normal and Cystic Fibrosis Superficial Airway Epithelia
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Soluble Mediators Not Cilia Determine Airway Surface Liquid Volume in Normal and Cystic Fibrosis Superficial Airway Epithelia

机译:可溶性调解员而非纤毛确定正常和囊性纤维化浅表气道上皮中的气道表面液量

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摘要

A key aspect of the lung's innate defense system is the ability of the superficial epithelium to regulate airway surface liquid (ASL) volume to maintain a 7-μm periciliary liquid layer (PCL), which is required for cilia to beat and produce mucus flow. The mechanisms whereby airway epithelia regulate ASL height to ≥7 μm are poorly understood. Using bumetanide as an inhibitor of Cl secretion, and nystatin as an activator of Na+ absorption, we found that a coordinated “blending” of both Cl secretion and Na+ absorption must occur to effect ASL volume homeostasis. We then investigated how ASL volume status is regulated by the underlying epithelia. Cilia were not critical to this process as (a) ASL volume was normal in cultures from patients with primary ciliary dyskinesia with immotile cilia, and (b) in normal cultures that had not yet undergone ciliogenesis. However, we found that maneuvers that mimic deposition of excess ASL onto the proximal airways, which occurs during mucociliary clearance and after glandular secretion, acutely stimulated Na+ absorption, suggesting that volume regulation was sensitive to changes in concentrations of soluble mediators in the ASL rather than alterations in ciliary beating. To investigate this hypothesis further, we added potential “soluble mediators” to the ASL. ASL volume regulation was sensitive to a channel-activating protein (CAP; trypsin) and a CAP inhibitor (aprotinin), which regulated Na+ absorption via changes in epithelial Na+ channel (ENaC) activity in both normal and cystic fibrosis cultures. ATP was also found to acutely regulate ASL volume by inducing secretion in normal and cystic fibrosis (CF) cultures, while its metabolite adenosine (ADO) evoked secretion in normal cultures but stimulated absorption in CF cultures. Interestingly, the amount of ASL/Cl secretion elicited by ATP/ADO was influenced by the level of CAP-induced Na+ absorption, suggesting that there are important interactions between the soluble regulators which finely tune ASL volume.
机译:肺的先天防御系统的一个关键方面是浅表上皮调节气道表面液(ASL)体积以维持7μm睫状液周层(PCL)的能力,这是纤毛敲打并产生粘液流动所必需的。气道上皮将ASL高度调节至≥7μm的机制了解甚少。使用布美他尼作为Cl -分泌的抑制剂,而制霉菌素作为抑制Na + 吸收的活化剂,我们发现Cl -必须发生/ sup>分泌和Na + 吸收,才能实现ASL体积稳态。然后,我们研究了基础上皮细胞如何调节ASL的体积状态。纤毛对这一过程并不重要,因为(a)原发性纤毛运动障碍伴有运动性纤毛的患者的ASL量正常,以及(b)尚未经历纤毛发生的正常培养物中。然而,我们发现,这种模拟在粘膜纤毛清除过程中和腺体分泌后发生的过量ASL沉积在近端气道上的动作,会急剧刺激Na + 吸收,这表明体积调节对浓度变化敏感。在ASL中的可溶性介体,而不是睫状跳动的改变。为了进一步研究该假设,我们向ASL添加了潜在的“可溶性介体”。 ASL的体积调节对通道激活蛋白(CAP;胰蛋白酶)和CAP抑制剂(抑肽酶)敏感,后者通过改变上皮Na + 通道来调节Na + 的吸收。 (ENaC)在正常和囊性纤维化培养物中的活性。还发现ATP通过诱导正常和囊性纤维化(CF)培养物中的分泌来急性调节ASL量,而其代谢腺苷(ADO)引起正常培养物中的分泌,但刺激CF培养物中的吸收。有趣的是,由ATP / ADO引起的ASL / Cl -分泌量受CAP诱导的Na + 吸收水平的影响,表明两者之间存在重要的相互作用。可溶性调节剂,可微调ASL的体积。

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