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气道上皮细胞氯离子通道的钙离子依赖性激活不依赖于磷酸化的证据。

Evidence that Ca2(+)-dependent activation of airway epithelia Cl- channels is not dependent on phosphorylation.

作者信息

Clancy J P, McCann J D, Welsh M J

机构信息

Howard Hughes Medical Institute, Department of Internal Medicine, University of Iowa College of Medicine, Iowa City 52242.

出版信息

Am J Physiol. 1990 Dec;259(6 Pt 1):L410-4. doi: 10.1152/ajplung.1990.259.6.L410.

Abstract

Previous studies have shown that an increase in the cytosolic Ca2+ concentration [( Ca2+]c) activates Cl- channels in airway epithelia but that the effect is indirect. Because adenosine 3',5'-cyclic monophosphate (cAMP) and phorbol myristate acetate (PMA) activate Cl- channels via phosphorylation by cAMP-dependent protein kinase and protein kinase C, respectively, we asked whether Ca2(+)-dependent Cl- channel activation is phosphorylation dependent. We measured 125I- efflux as an assay of Cl- channel activation in the intact cell. We found that depletion of cellular ATP prevented cAMP- and PMA-induced activation but did not alter activation produced by the Ca2+ ionophore A23187. Moreover, addition of high concentrations of staurosporine (5 microM), to nonspecifically inhibit kinase activity, blocked cAMP- and PMA-stimulated 125I- efflux but had no effect on A23187-induced efflux. These results suggest that elevation of [Ca2+]c does not activate Cl- channels via phosphorylation.

摘要

以往的研究表明,胞质Ca2+浓度([Ca2+]c)的升高会激活气道上皮细胞中的Cl-通道,但这种作用是间接的。由于3',5'-环磷酸腺苷(cAMP)和佛波醇肉豆蔻酸酯乙酸盐(PMA)分别通过cAMP依赖性蛋白激酶和蛋白激酶C的磷酸化作用来激活Cl-通道,因此我们探讨了Ca2+依赖性Cl-通道激活是否依赖于磷酸化。我们通过测量完整细胞中125I的外流来检测Cl-通道的激活情况。我们发现,细胞内ATP的耗竭会阻止cAMP和PMA诱导的激活,但不会改变Ca2+离子载体A23187所产生的激活作用。此外,加入高浓度的星形孢菌素(5μM)以非特异性抑制激酶活性,可阻断cAMP和PMA刺激的125I外流,但对A23187诱导的外流没有影响。这些结果表明,[Ca2+]c的升高不会通过磷酸化作用来激活Cl-通道。

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