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在经fura-2负载的豚鼠心室肌细胞中,细胞内钙离子浓度([Ca2+]i)对单一L型钙离子通道电流的双重调制

Dual modulation of unitary L-type Ca2+ channel currents by [Ca2+]i in fura-2-loaded guinea-pig ventricular myocytes.

作者信息

Hirano Y, Hiraoka M

机构信息

Department of Cardiovascular Diseases, Tokyo Medical and Dental University, Japan.

出版信息

J Physiol. 1994 Nov 1;480 ( Pt 3)(Pt 3):449-63. doi: 10.1113/jphysiol.1994.sp020374.

Abstract
  1. Single-channel studies were performed to clarify how tonic changes in intracellular Ca2+ concentrations ([Ca2+]i) modulate cardiac L-type Ca2+ channels. Currents were recorded from fura-2-loaded guinea-pig ventricular myocytes in the cell-attached configuration. Fura-2 fluorescence signals were recorded simultaneously during pulses to elicit channel activity. 2. The myocyte [Ca2+]i was altered through changes in bath Ca2+ concentration during K+ depolarization. When [Ca2+]i exceeded approximately 2 times the resting level (estimated [Ca2+]i around 180-400 nM), the activity of Ca2+ channels was reversibly potentiated without changes in unitary current amplitudes. 3. Increased channel open probability during Ca(2+)-dependent potentiation resulted from increased availability and increased open probability during non-blank sweeps. Closed time analysis revealed a distribution best fitted with two exponentials. Increased [Ca2+]i reduced the longer time constant, but had no effect on the shorter time constant. The open time constant was unchanged in most cases. Current records occasionally included sweeps with long openings (approximately 10 ms or more), whose appearance increased during potentiation. 4. When [Ca2+]i was increased after cAMP-dependent upregulation of Ca2+ channels, the change in channel activity was diminished. Similar results were observed when Ca(2+)-dependent potentiation was examined in myocytes exposed to a membrane-permeant protein kinase inhibitor, H-89. This suggests that channel phosphorylation may be responsible for Ca(2+)-dependent potentiation. 5. When [Ca2+]i was further increased, but remained below the threshold for contraction (estimated [Ca2+]i above 600 nM), Ca2+ channel activity was suppressed. 6. Our results demonstrate directly at the single-channel level that [Ca2+]i modulates the activity of cardiac L-type Ca2+ channels, enhancing it with modest [Ca2+]i increases and decreasing it with greater [Ca2+]i increases.
摘要
  1. 进行了单通道研究,以阐明细胞内Ca2+浓度([Ca2+]i)的强直变化如何调节心脏L型Ca2+通道。在细胞贴附模式下,从负载fura-2的豚鼠心室肌细胞记录电流。在引发通道活性的脉冲期间,同时记录fura-2荧光信号。2. 在K+去极化期间,通过改变浴液Ca2+浓度来改变心肌细胞的[Ca2+]i。当[Ca2+]i超过静息水平的约2倍(估计[Ca2+]i约为180 - 400 nM)时,Ca2+通道的活性可逆增强,而单通道电流幅度无变化。3. Ca(2+)依赖性增强期间通道开放概率的增加是由于非空白扫描期间可用性增加和开放概率增加。关闭时间分析显示,分布最适合两个指数函数。[Ca2+]i增加会降低较长的时间常数,但对较短的时间常数没有影响。在大多数情况下,开放时间常数不变。电流记录偶尔包括长开放(约10 ms或更长)的扫描,其出现次数在增强期间增加。4. 当在cAMP依赖性上调Ca2+通道后增加[Ca2+]i时,通道活性的变化减弱。当在暴露于膜通透性蛋白激酶抑制剂H-89的心肌细胞中检查Ca(2+)依赖性增强时,观察到类似结果。这表明通道磷酸化可能是Ca(2+)依赖性增强的原因。5. 当[Ca2+]i进一步增加,但仍低于收缩阈值(估计[Ca2+]i高于600 nM)时,Ca2+通道活性受到抑制。6. 我们的结果在单通道水平直接证明,[Ca2+]i调节心脏L型Ca2+通道的活性,适度增加[Ca2+]i时增强其活性,而更大程度增加[Ca2+]i时降低其活性。

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