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β2-adrenergic regulation of ciliary beat frequency in rat bronchiolar epithelium: potentiation by isosmotic cell shrinkage

机译:β2-肾上腺素调节大鼠细支气管上皮纤毛搏动频率:等渗细胞收缩增强

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摘要

Single bronchiolar ciliary cells were isolated from rat lungs. The β2-adrenergic regulation of ciliary beat frequency (CBF) was studied using video-optical microscopy. Terbutaline (a β2-adrenergic agonist) increased CBF in a dose-dependent manner, and it also decreased the volume of the ciliary cells. These terbutaline actions were inhibited by a PKA inhibitor (H-89) and mimicked by forskolin, IBMX and DBcAMP. Ion transport inhibitors were used to isosmotically manipulate the volume of the terbutaline-stimulated bronchiolar ciliary cells. Amiloride (1 μm) and bumetanide (20 μm) potentiated cell shrinkage and the CBF increase, and they shifted the terbutaline dose–response curve to the lower-concentration side. Quinidine (500 μm), in contrast, increased cell volume and suppressed the CBF increase. Moreover, a KCl solution containing amiloride (1 μm) and strophanthidin (100 μm) increased cell volume and suppressed the CBF increase, and then the subsequent removal of either amiloride or strophanthidin decreased cell volume and further increased CBF. NPPB (10 μm) or glybenclamide (200 μm) had no effect on the action of terbutaline. Thus, in terbutaline-stimulated ciliary cells, cell shrinkage enhances the CBF increase; in contrast, cell swelling suppresses it. However, the results of direct manupulation of cell volume by applying osmotic stresses (hyperosmotic shrinkage or hyposmotic swelling) were the opposite of the findings of the isosmotic experiments: hyposmotic cell swelling enhanced the CBF increase, while isosmotic swelling suppressed it. These results suggest that isosmotic and non-isosmotic volume changes in terbutaline-stimulated bronchiolar ciliary cells may trigger different signalling pathways. In conclusion, terbutaline increases CBF and decreases the volume of rat bronchiolar ciliary cells via cAMP accumulation under isosmotic conditions, and the isosmotic cell shrinkage enhances the CBF increase by increasing cAMP sensitivity.
机译:从大鼠肺中分离出单个支气管纤毛细胞。使用视频光学显微镜研究了β2-肾上腺素对纤毛搏动频率(CBF)的调节。特布他林(β2-肾上腺素能激动剂)以剂量依赖的方式增加脑血流量,也减少了睫状细胞的体积。这些特布他林的作用被PKA抑制剂(H-89)抑制,并被毛喉素,IBMX和DBcAMP模仿。离子转运抑制剂被用于等渗地调节特布他林刺激的细支气管纤毛细胞的体积。阿米洛利(1μm)和布美他尼(20μm)增强了细胞的收缩并增加了脑血流,并且它们将特布他林的剂量反应曲线移至较低浓度一侧。相反,奎尼丁(500μm)可增加细胞体积并抑制CBF的增加。此外,含有阿米洛利(1μm)和鸟嘌呤(100μm)的KCl溶液可增加细胞体积并抑制CBF的增加,然后随后去除阿米洛利或鸟嘌呤可降低细胞体积并进一步增加CBF。 NPPB(10μm)或格列苯脲(200μm)对特布他林的作用没有影响。因此,在特布他林刺激的睫状细胞中,细胞收缩促进了CBF的增加。相反,细胞肿胀会抑制它。然而,通过施加渗透压力(高渗性收缩或低渗性肿胀)直接调节细胞体积的结果与等渗实验的发现相反:低渗性细胞肿胀增强了CBF的增加,而等渗性肿胀则抑制了CBF的增加。这些结果表明,特布他林刺激的细支气管纤毛细胞的等渗和非等渗体积变化可能触发不同的信号通路。总之,特布他林在等渗条件下通过cAMP积累增加了CBF并减少了大鼠细支气管纤毛细胞的体积,等渗细胞的收缩通过增加cAMP敏感性提高了CBF的增加。

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