Although earlier studies with phorbol esters indicate that protein kinase C (PKC) may be an important regulator of Cl- current (Icl) in cardiac cells, there is a need for additional quantitative data and investigation of conflicting findings. Our objectives were to measure the magnitude, time course, and concentration-dependence of Icl activated in guinea-pig ventricular myocytes by phorbol 12-myristate 13-acetate (PMA), evaluate its PKC dependence, and examine its modification by external and internal ions. 2. The whole-cell patch clamp technique was used to apply short depolarizing and hyperpolarizing pulses to myocytes superfused with Na(+)-, K(+)-, Ca(2+)-free solution (36 degrees C) and dialysed with Cs+ solution. Stimulation of membrane currents by PMA (threshold < or = 1nM, EC50 approximately equal to 14 nM, maximal 40% increase with > or = 100 nM) plateaued within 6-10 min. 3. PMA-activated current was time-independent, and suppressed by l mM 9-anthracenecarboxylic acid (9-AC). Its reversal potential (Erev) was sensitive to changes in the Cl- gradient, and outward rectification of the current-voltage (I-V) relationship was more pronounced with 30 mM than 140 mM Cl- dialysate. 4. The relative permeability of PMA-activated channels estimated from Erev measurements was I- > Cl- > > aspartate. Channel activation was independent of external Na+. 5. PMA failed to activate Icl in myocytes pretreated with 1-(5-isoquinolinesulfonyl)-2-methylpiperazine (H-7) or dialysed with pCa 10.5 solution. Lack of response to 4 alpha-phorbol 12, 13-didecanoate (alpha PDD) was a further indication of mediation by PKC. 6. Icl induced by 2 microM forskolin was far larger than that induced by PMA, suggesting that endogenous protein kinase A is a much stronger Cl- channel activator than endogenous PKC in these myocytes. 7. The macroscopic properties of PMA-induced Icl appear to be indistinguishable from those of PKA-activated Icl. We discount stimulation of PKA by PMA as an explanation, and conclude that endogenous PKC may activate PKA-regulated Cl- channels in these myocytes.
摘要
尽管早期使用佛波酯的研究表明蛋白激酶C(PKC)可能是心脏细胞中氯离子电流(Icl)的重要调节因子,但仍需要更多定量数据并对相互矛盾的研究结果进行调查。我们的目标是测量12-肉豆蔻酸佛波醇13-乙酸酯(PMA)激活豚鼠心室肌细胞中Icl的幅度、时间进程和浓度依赖性,评估其对PKC的依赖性,并研究外部和内部离子对其的修饰作用。2. 采用全细胞膜片钳技术,向用无Na⁺、K⁺、Ca²⁺溶液(36℃)灌流并用Cs⁺溶液透析的心肌细胞施加短暂的去极化和超极化脉冲。PMA对膜电流的刺激(阈值≤1 nM,EC50约等于14 nM,≥100 nM时最大增加40%)在6 - 10分钟内达到平稳。3. PMA激活的电流与时间无关,并被1 mM 9-蒽甲酸(9-AC)抑制。其反转电位(Erev)对Cl⁻梯度的变化敏感,与140 mM Cl⁻透析液相比,30 mM Cl⁻透析液时电流-电压(I-V)关系的外向整流更明显。4. 根据Erev测量估算,PMA激活通道的相对通透性为I⁻>Cl⁻>>天冬氨酸。通道激活与外部Na⁺无关。5. PMA在用1-(5-异喹啉磺酰基)-2-甲基哌嗪(H-7)预处理或用pCa 10.5溶液透析的心肌细胞中未能激活Icl。对4α-佛波醇12,13-二癸酸酯(αPDD)无反应进一步表明是由PKC介导的。6. 2 μM福斯高林诱导的Icl远大于PMA诱导的Icl,表明在这些心肌细胞中内源性蛋白激酶A是比内源性PKC更强的Cl⁻通道激活剂。7. PMA诱导的Icl的宏观特性似乎与PKA激活的Icl无法区分。我们排除PMA刺激PKA作为解释,并得出结论:内源性PKC可能在这些心肌细胞中激活PKA调节的Cl⁻通道。