Kunzelmann K, Koslowsky T, Hug T, Gruenert D C, Greger R
Physiologisches Institut, Albert-Ludwigs-Universität Freiburg, Germany.
Pflugers Arch. 1994 Oct;428(5-6):590-6. doi: 10.1007/BF00374582.
The cAMP-dependent activation of Cl- channels was studied in a bronchial epithelial cell line (16HBE14o-) in fast and slow whole-cell, and cell-attached patch-clamp experiments. The cells are known to express high levels of cystic fibrosis transmembrane conductance regulator mRNA and protein. Isoproterenol, forskolin and histamine (all 10 mumol/l) reversibly and significantly depolarized the membrane voltage (Vm) and increased the whole-cell Cl- conductance significantly by 34.0 +/- 0.9 (n = 3), 18.1 +/- 2.7 (n = 50), and 25 +/- 4.5 (n = 37) nS respectively. The effect of histamine was blocked by cimetidine (10 mumol, n = 5) but not by diphenhydramine (10 mumol/l, n = 4), which suggests binding of histamine to H2 receptors. The forskolin-induced current was not inhibited significantly by 4,4'-diisothiocyanatostilbene-2,2'-disulphonic acid (0.5 mmol/l, n = 9) nor glibenclamide (10 mumol/l, n = 3) and had an anion-permeability sequence of Cl = Br- > I- (n = 9). In cell-attached recordings forskolin (10 mumol/l) increased the conductance of the patched membrane from 65.5 +/- 13.6 pS to 150.8 +/- 33.2 pS (n = 30). Although the conductance was increased significantly, clear ion channel events occurring in parallel with the current activation were not detected in the cell-attached membrane. In 4 out of 30 cell-attached recordings single-channel currents were observed. These channels, with a single-channel conductance of about 6 pS, were already active before forskolin was added. No effect of forskolin on the channel amplitude, open probability or kinetics of these channels was observed.(ABSTRACT TRUNCATED AT 250 WORDS)
在快速和慢速全细胞以及细胞贴附式膜片钳实验中,对支气管上皮细胞系(16HBE14o-)中依赖环磷酸腺苷(cAMP)的氯离子通道激活进行了研究。已知这些细胞表达高水平的囊性纤维化跨膜传导调节因子mRNA和蛋白质。异丙肾上腺素、福斯高林和组胺(均为10μmol/L)可使膜电压(Vm)可逆性地显著去极化,并分别使全细胞氯离子传导率显著增加34.0±0.9(n = 3)、18.1±2.7(n = 50)和25±4.5(n = 37)nS。组胺的作用可被西咪替丁(10μmol,n = 5)阻断,但不能被苯海拉明(10μmol/L,n = 4)阻断,这表明组胺与H2受体结合。福斯高林诱导的电流不受4,4'-二异硫氰基芪-2,2'-二磺酸(0.5mmol/L,n = 9)或格列本脲(10μmol/L,n = 3)的显著抑制,其阴离子通透性顺序为Cl = Br- > I-(n = 9)。在细胞贴附式记录中,福斯高林(10μmol/L)使膜片膜电导从65.5±13.6pS增加到150.8±33.2pS(n = 30)。尽管电导显著增加,但在细胞贴附膜中未检测到与电流激活同时发生的明显离子通道事件。在30次细胞贴附式记录中的4次中观察到了单通道电流。这些通道的单通道电导约为6pS,在添加福斯高林之前就已经处于激活状态。未观察到福斯高林对这些通道的幅度、开放概率或动力学有影响。(摘要截断于250字)