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气道上皮黏液颗粒中包含一系列腺嘌呤核苷酸的受体促进的胞吐作用。

Receptor-promoted exocytosis of airway epithelial mucin granules containing a spectrum of adenine nucleotides.

机构信息

Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina at Chapel Hill, 4029A Thurston Bowles Building, Chapel Hill, NC 27599-7248, USA.

出版信息

J Physiol. 2010 Jun 15;588(Pt 12):2255-67. doi: 10.1113/jphysiol.2009.186643. Epub 2010 Apr 26.

Abstract

Purinergic regulation of airway innate defence activities is in part achieved by the release of nucleotides from epithelial cells. However, the mechanisms of airway epithelial nucleotide release are poorly understood. We have previously demonstrated that ATP is released from ionomycin-stimulated airway epithelial goblet cells coordinately with mucin exocytosis, suggesting that ATP is released as a co-cargo molecule from mucin-containing granules. We now demonstrate that protease-activated-receptor (PAR) agonists also stimulate the simultaneous release of mucins and ATP from airway epithelial cells. PAR-mediated mucin and ATP release were dependent on intracellular Ca(2+) and actin cytoskeleton reorganization since BAPTA AM, cytochalasin D, and inhibitors of Rho and myosin light chain kinases blocked both responses. To test the hypothesis that ATP is co-released with mucin from mucin granules, we measured the nucleotide composition of isolated mucin granules purified based on their MUC5AC and VAMP-8 content by density gradients. Mucin granules contained ATP, but the levels of ADP and AMP within granules exceeded by nearly 10-fold that of ATP. Consistent with this finding, apical secretions from PAR-stimulated cells contained relatively high levels of ADP/AMP, which could not be accounted for solely based on ATP release and hydrolysis. Thus, mucin granules contribute to ATP release and also are a source of extracellular ADP and AMP. Direct release of ADP/AMP from mucin granules is likely to provide a major source of airway surface adenosine to signal in a paracrine faction ciliated cell A(2b) receptors to activate ion/water secretion and appropriately hydrate goblet cell-released mucins.

摘要

嘌呤能调节气道先天防御活动的部分机制是通过上皮细胞释放核苷酸来实现的。然而,气道上皮细胞核苷酸释放的机制还不清楚。我们之前已经证明,在离子霉素刺激的气道上皮杯状细胞中,ATP 与粘蛋白分泌一起释放,这表明 ATP 作为粘蛋白颗粒中的共同载体分子释放。我们现在证明,蛋白酶激活受体 (PAR) 激动剂也能刺激气道上皮细胞同时释放粘蛋白和 ATP。PAR 介导的粘蛋白和 ATP 释放依赖于细胞内 Ca(2+)和肌动蛋白细胞骨架的重组,因为 BAPTA AM、细胞松弛素 D 和 Rho 和肌球蛋白轻链激酶的抑制剂阻断了这两种反应。为了验证 ATP 是与粘蛋白从粘蛋白颗粒中共释放的假设,我们测量了通过密度梯度根据其 MUC5AC 和 VAMP-8 含量纯化的分离粘蛋白颗粒中的核苷酸组成。粘蛋白颗粒含有 ATP,但颗粒内 ADP 和 AMP 的水平比 ATP 高出近 10 倍。与这一发现一致的是,PAR 刺激细胞的顶端分泌物中含有相对较高水平的 ADP/AMP,这不能仅根据 ATP 释放和水解来解释。因此,粘蛋白颗粒有助于 ATP 的释放,也是细胞外 ADP 和 AMP 的来源。粘蛋白颗粒的直接释放可能为气道表面腺苷提供主要来源,以旁分泌方式激活纤毛细胞 A(2b)受体,从而激活离子/水分泌并适当水合杯状细胞释放的粘蛋白。

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