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cGMP modulation of ACh-stimulated exocytosis in guinea pig antral mucous cells.

机译:cGMP调节豚鼠肛门粘膜细胞中ACh刺激的胞吐作用。

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In guinea pig antral mucous cells, ACh stimulates the Ca(2+)-regulated exocytosis, which has a characteristics feature: an initial transient phase followed by a sustained phase. The effects of cGMP on ACh-stimulated exocytosis were studied in guinea pig antral mucous cells using video microscopy. cGMP enhanced the frequency of ACh-stimulated exocytotic events, whereas cGMP alone did not induce any exocytotic events under the ACh-unstimulated condition. cGMP did not stimulate either Ca(2+) mobilization or cAMP accumulation. The Ca(2+) dose-response studies demonstrated that cGMP shifted the dose-response curve upward with no shift to the lower concentration. This indicates that cGMP increased maximal responsiveness of the Ca(2+)-regulated exocytosis, but not the Ca(2+) sensitivity. Moreover, under a condition of ATP depletion by dinitrophenol (DNP) or anoxia (N(2) bubbling), ACh evoked only a sustained phase in exocytotic events with no initial transient phase. However, ACh evoked an initial transient phase followed by a sustained phase with addition of cGMP before ATP depletion, whereas only a sustained phase was evoked in a case of cGMP addition after ATP depletion. Thus cGMP-induced enhancement in ACh-stimulated exocytotic events requires ATP, suggesting that cGMP modulates ATP-dependent priming of Ca(2+)-regulated exocytosis in antral mucous cells. In conclusion, cGMP increases the number of primed granules via acceleration of the ATP-dependent priming, which enhances the Ca(2+)-regulated exocytosis stimulated by ACh.
机译:在豚鼠肛门黏液细胞中,ACh刺激Ca(2+)调控的胞吐作用,该胞吐作用具有以下特征:最初的过渡期,然后是持续期。使用视频显微镜研究了豚鼠肛门粘膜细胞中cGMP对ACh刺激的胞吐作用的影响。 cGMP增加了ACh刺激的胞吐事件的频率,而单独的cGMP在ACh不受刺激的条件下不诱导任何胞吐事件。 cGMP不会刺激Ca(2+)动员或cAMP积累。 Ca(2+)剂量反应研究表明,cGMP将剂量反应曲线向上移动,而没有向较低浓度移动。这表明cGMP增加了Ca(2+)调节的胞吐作用的最大反应能力,但没有Ca(2+)敏感性。此外,在二硝基苯酚(DNP)或缺氧(N(2)鼓泡)消耗ATP的条件下,乙酰胆碱酯酶仅在胞吐事件中诱发持续阶段,而没有初始过渡阶段。但是,ACh诱发了一个初始过渡阶段,随后是一个持续阶段,在ATP耗尽之前添加了cGMP,而在ATP耗尽之后添加cGMP的情况下,仅诱发了一个持续阶段。因此,cGMP诱导的ACh刺激的胞吐事件的增强需要ATP,表明cGMP调节胃黏膜细胞中Ca(2+)调节的胞吐作用的ATP依赖性启动。总之,cGMP通过加速ATP依赖的引发作用而增加了引发剂颗粒的数量,从而增强了由ACh刺激的Ca(2+)调控的胞吐作用。

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