García-Díaz J F
Department of Physiology, Boston University School of Medicine, Massachusetts 02118.
J Gen Physiol. 1991 Jul;98(1):131-61. doi: 10.1085/jgp.98.1.131.
Whole-cell and single channel currents were studied in cells from frog (R. pipiens and R. catesbiana) skin epithelium, isolated by collagenase and trypsin treatment, and kept in primary cultures up to three days. Whole-cell currents did not exhibit any significant time-dependent kinetics under any ionic conditions used. With an external K gluconate Ringer solution the currents showed slight inward rectification with a reversal potential near zero and an average conductance of 5 nS at reversal. Ionic substitution of the external medium showed that most of the cell conductance was due to K and that very little, if any, Na conductance was present. This confirmed that most cells originate from inner epithelial layers and contain membranes with basolateral properties. At voltages more positive than 20 mV outward currents were larger with K in the medium than with Na or N-methyl-D-glucamine. Such behavior is indicative of a multi-ion transport mechanism. Whole-cell K current was inhibited by external Ba and quinidine. Blockade by Ba was strongly voltage dependent, while that by quinidine was not. In the presence of high external Cl, a component of outward current that was inhibited by the anion channel blocker diphenylamine-2-carboxylate (DPC) appeared in 70% of the cells. This component was strongly outwardly rectifying and reversed at a potential expected for a Cl current. At the single channel level the event most frequently observed in the cell-attached configuration was a K channel with the following characteristics: inward-rectifying I-V relation with a conductance (with 112.5 mM K in the pipette) of 44 pS at the reversal potential, one open and at least two closed states, and open probability that increased with depolarization. Quinidine blocked by binding in the open state and decreasing mean open time. Several observations suggest that this channel is responsible for most of the whole-cell current observed in high external K, and for the K conductance of the basolateral membrane of the intact epithelium. On a few occasions a Cl channel was observed that activated upon excision and brief strong depolarization. The I-V relation exhibited strong outward rectification with a single channel conductance of 48 pS at 0 mV in symmetrical 112 mM Cl solutions. Kinetic analysis showed the presence of two open and at least two closed states. Open time constants and open probability increased markedly with depolarization.(ABSTRACT TRUNCATED AT 400 WORDS)
对经胶原酶和胰蛋白酶处理后分离出来的牛蛙(R. pipiens和R. catesbiana)皮肤上皮细胞进行全细胞和单通道电流研究,并将其原代培养长达三天。在所使用的任何离子条件下,全细胞电流均未表现出任何明显的时间依赖性动力学。在外部为葡萄糖酸钾林格溶液时,电流显示出轻微的内向整流,反转电位接近零,反转时平均电导为5 nS。外部介质的离子替代表明,细胞的大部分电导归因于钾,几乎不存在钠电导(如果有,也极少)。这证实了大多数细胞起源于内上皮层,且含有具有基底外侧特性的膜。在电压高于20 mV时,介质中含钾时的外向电流大于含钠或N-甲基-D-葡萄糖胺时的外向电流。这种行为表明存在多离子转运机制。全细胞钾电流受到外部钡和奎尼丁的抑制。钡的阻断强烈依赖电压,而奎尼丁的阻断则不依赖电压。在外部高氯存在的情况下,70%的细胞中出现了一种被阴离子通道阻滞剂二苯胺-2-羧酸盐(DPC)抑制的外向电流成分。该成分具有强烈的外向整流特性,且在预期的氯离子电流电位处反转。在单通道水平上,在细胞贴附模式下最常观察到的事件是一个具有以下特征的钾通道:内向整流的电流-电压关系,在反转电位下(移液管中含112.5 mM钾)电导为44 pS,一个开放状态和至少两个关闭状态,开放概率随去极化增加。奎尼丁通过在开放状态下结合并缩短平均开放时间来阻断。一些观察结果表明,该通道负责在外部高钾时观察到的大部分全细胞电流,以及完整上皮基底外侧膜的钾电导。有几次观察到一个氯离子通道,在切除和短暂强烈去极化后被激活。在对称的112 mM氯溶液中,电流-电压关系表现出强烈的外向整流,在0 mV时单通道电导为48 pS。动力学分析表明存在两个开放状态和至少两个关闭状态。开放时间常数和开放概率随去极化显著增加。(摘要截断于400字)