Wang W H, Schwab A, Giebisch G
Department of Cellular and Molecular Physiology, Yale University Medical School, New Haven, Connecticut 06510.
Am J Physiol. 1990 Sep;259(3 Pt 2):F494-502. doi: 10.1152/ajprenal.1990.259.3.F494.
We used the patch-clamp technique to study the activity and regulation of single potassium channels in the apical membrane of isolated cortical collecting tubules (CCT) of rat kidney. With 140 mM K+ in the pipette the inward conductance of the channel in cell-attached patches at 37 degrees C was 35 pS (n = 106, NaCl-Ringer or 70 mM KCl and 70 mM NaCl in the bath), and the outward conductance was 15 pS (n = 15, 70 mM NaCl + 70 mM KCl in the bath). Mean open probability (Po) of the channel is voltage independent and 0.96 (n = 106). The channel displayed one open state with a mean lifetime of 18.6 ms and one closed state with a mean lifetime of 0.7 ms (n = 20). Selectivity ratio between K+ and Na+ is 20 (n = 5). High-potassium diet increased channel incidence from control 32% (53 patches with channel from 165 patches) to 64% (53 patches with channels from 83 patches). The channel could be blocked by 1 mM Ba2+ (n = 7, Ba2+ in the pipette); however, 5 mM tetraethylammonium (n = 9, TEA in the pipette) did not block the channel activity. The channel was very sensitive to intracellular pH (n = 6). Changing bath pH facing cytoplasmic side of inside-out patches from 7.4 to 6.9 reversibly reduced Po from 0.9 to 0.1. Addition of 1 mM ATP (n = 7) to bath almost completely inhibited channel activity in inside-out patches. This ATP-induced inhibition was fully reversible and was found to be dependent on the ratio of ATP to ADP, since adding 0.5 mM ADP to bath solution relieved the ATP-induced blockade. Results indicate that intracellular pH, concentration of ATP, and ratio of ATP to ADP are important regulators of potassium channel activity in the apical membrane of rat CCT, and the properties of the channel make it a strong candidate for K+ secretion in this nephron segment.
我们运用膜片钳技术研究大鼠肾皮质集合管(CCT)顶端膜中单个钾通道的活性及调节机制。移液管内钾离子浓度为140 mM时,在37℃下,细胞贴附式膜片中通道的内向电导为35 pS(n = 106,浴槽中为NaCl - 林格液或70 mM KCl和70 mM NaCl),外向电导为15 pS(n = 15,浴槽中为70 mM NaCl + 70 mM KCl)。通道的平均开放概率(Po)与电压无关,为0.96(n = 106)。该通道呈现一个平均寿命为18.6 ms的开放状态和一个平均寿命为0.7 ms的关闭状态(n = 20)。钾离子与钠离子的选择性比率为20(n = 5)。高钾饮食使通道出现率从对照组的32%(165个膜片中53个有通道)增至64%(83个膜片中53个有通道)。该通道可被移液管内的1 mM Ba2+阻断(n = 7);然而,移液管内的5 mM四乙铵(n = 9,TEA)并未阻断通道活性。该通道对细胞内pH非常敏感(n = 6)。将内面向外膜片面向细胞质一侧的浴槽pH从7.4变为6.9,可使Po从0.9可逆性降至0.1。向浴槽中添加1 mM ATP(n = 7)几乎完全抑制内面向外膜片中的通道活性。这种ATP诱导的抑制作用完全可逆,且发现其依赖于ATP与ADP的比率,因为向浴槽溶液中添加0.5 mM ADP可解除ATP诱导的阻断。结果表明,细胞内pH、ATP浓度以及ATP与ADP的比率是大鼠CCT顶端膜中钾通道活性的重要调节因子,且该通道的特性使其成为此肾单位段钾分泌的有力候选者。