McCann J D, Welsh M J
Howard Hughes Medical Institute, Department of Physiology, University of Iowa College of Medicine, Iowa City 52242.
Am J Physiol. 1990 Jun;258(6 Pt 1):L343-8. doi: 10.1152/ajplung.1990.258.6.L343.
We previously described a Ca2(+)-activated K+ channel (KCLIC) in airway epithelial cells [J. D. McCann, J. Matsuda, M. Garcia, G. Kaczorowski, and M. J. Welsh. Am. J. Physiol 258 (Lung Cell. Mol. Physiol. 2): L334-L342, 1990]. To determine whether the KCLIC channel is a basolateral membrane channel and to understand its role in Cl- secretion, we studied airway epithelial cells grown on permeable supports. When cells were stimulated with A23187, charybdotoxin (ChTX) inhibited Cl- secretion and 86Rb efflux at the same concentrations, indicating that the KCLIC channel is required for Ca2(+)-stimulated Cl- secretion. We also investigated the function of K+ channels in adenosine 3',5'-cyclic monophosphate-stimulated secretion. Addition of isoproterenol caused a biphasic increase in Cl- secretion; the time course of the transient component correlated with the time course of the isoproterenol-induced increase in Ca2+ concentration [( Ca2+]c). ChTX inhibited the transient component, but not the prolonged component of secretion; Ba2+ inhibited the sustained component. These results suggest that when cells are grown on permeable supports isoproterenol-induced secretion depends on activation of two types of K+ channel: the KCLIC channel that is stimulated initially and a ChTX-insensitive K+ channel that is stimulated during sustained secretion. This conclusion was supported by measurement of 86Rb efflux from cell monolayers.
我们之前曾描述过气道上皮细胞中的一种钙激活钾通道(KCLIC)[J.D. 麦肯、J. 松田、M. 加西亚、G. 卡佐罗夫斯基和M.J. 威尔士。《美国生理学杂志》258(肺细胞与分子生理学2):L334 - L342,1990年]。为了确定KCLIC通道是否为基底外侧膜通道,并了解其在氯离子分泌中的作用,我们研究了在可渗透支持物上生长的气道上皮细胞。当用A23187刺激细胞时,章鱼毒素(ChTX)在相同浓度下抑制氯离子分泌和86Rb外流,表明KCLIC通道是钙刺激氯离子分泌所必需的。我们还研究了钾通道在腺苷3',5'-环磷酸单酯刺激分泌中的功能。加入异丙肾上腺素导致氯离子分泌出现双相增加;瞬态成分的时间进程与异丙肾上腺素诱导的细胞内钙浓度([Ca2+]c)增加的时间进程相关。ChTX抑制瞬态成分,但不抑制分泌的持续成分;Ba2+抑制持续成分。这些结果表明,当细胞在可渗透支持物上生长时,异丙肾上腺素诱导的分泌取决于两种类型钾通道的激活:最初被刺激的KCLIC通道和在持续分泌过程中被刺激的ChTX不敏感钾通道。细胞单层86Rb外流的测量结果支持了这一结论。