Cook D I, Poronnik P, Young J A
Department of Physiology, University of Sydney, NSW, Australia.
J Membr Biol. 1990 Mar;114(1):37-52. doi: 10.1007/BF01869383.
We have studied a 25-pS nonselective cation channel from the apical membranes of cell line ST885, derived from neonatal mouse mandibular glands. Its Cl- permeability was not significantly different from zero. The permeabilities (relative to Na+) for inorganic cations were NH4+ (1.87) greater than K+ (1.12) greater than Li+ (1.02) greater than Na+ (1) greater than Rb+ (0.81) greater than Mg2+ (0.07) greater than Ca2+ (0.002), and for organic cations, guanidinium (1.61) greater than ethanolamine (0.70) greater than 4-aminopyridine (0.66) greater than diethylamine (0.54) greater than piperazine (0.25) greater than Tris (0.18) greater than N-methylglucamine (0.12). The Tris and N-methylglucamine permeabilities differed significantly from zero. Fitting the Renkin equation indicated that the channel had an equivalent pore radius of 0.49 nm. The channel was activated by Ca2+ on the cytosolic surface (greater than 0.1 mmol/liter) with a Hill coefficient of 1.2; it was also activated by depolarization. Open- and closed-time histograms indicated that it had at least two open and two closed states. The channel was blocked by cytosolic AMP or ATP (0.1 mmol/liter). It was also blocked by the Cl- channel blocker, diphenylamine-2-carboxylate (DPC; 0.1 mmol/liter), applied to the extracellular but not the cytosolic surface. 4-Amino-pyridine, which permeated the channel when applied to the extracellular surface, blocked it when applied in low concentrations (5 mmol/liter) to the cytosolic surface. Quinine (0.1 mmol/liter) blocked from both the extracellular and cytosolic surfaces, blockade from either side being enhanced by depolarization. The channel was held open by application of SITS (0.1 mmol/liter) to the cytosolic surface. The channel shows striking similarities to the nicotinic acetylcholine receptor channel, viz., both channel types are abnormally permeable to 4-aminopyridine applied externally, and their selectivity sequences for inorganic ions are similar and for organic cations are identical.
我们研究了一种来自新生小鼠下颌腺细胞系ST885顶端膜的25皮秒非选择性阳离子通道。其氯离子通透性与零无显著差异。无机阳离子的通透性(相对于钠离子)顺序为:铵离子(1.87)大于钾离子(1.12)大于锂离子(1.02)大于钠离子(1)大于铷离子(0.81)大于镁离子(0.07)大于钙离子(0.002);有机阳离子的通透性顺序为:胍离子(1.61)大于乙醇胺(0.70)大于4-氨基吡啶(0.66)大于二乙胺(0.54)大于哌嗪(0.25)大于三羟甲基氨基甲烷(0.18)大于N-甲基葡糖胺(0.12)。三羟甲基氨基甲烷和N-甲基葡糖胺的通透性与零有显著差异。对伦金方程进行拟合表明该通道的等效孔径为0.49纳米。该通道在胞质表面被钙离子(大于0.1毫摩尔/升)激活,希尔系数为1.2;它也可被去极化激活。开放时间和关闭时间直方图表明它至少有两种开放状态和两种关闭状态。该通道被胞质中的AMP或ATP(0.1毫摩尔/升)阻断。它也被氯离子通道阻断剂二苯胺-2-羧酸盐(DPC;0.1毫摩尔/升)阻断,该阻断剂施加于细胞外表面而非胞质表面。4-氨基吡啶,当施加于细胞外表面时可通透该通道,而当以低浓度(5毫摩尔/升)施加于胞质表面时则阻断该通道。奎宁(0.1毫摩尔/升)从细胞外和胞质表面均可阻断该通道,去极化会增强从任一侧的阻断作用。通过向胞质表面施加SITS(0.1毫摩尔/升)可使该通道保持开放。该通道与烟碱型乙酰胆碱受体通道有显著相似之处,即两种通道类型对外源性施加的4-氨基吡啶均有异常通透性,并且它们对无机离子的选择性顺序相似,对有机阳离子的选择性顺序相同。