Rosenberg R L, Hess P, Tsien R W
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06510.
J Gen Physiol. 1988 Jul;92(1):27-54. doi: 10.1085/jgp.92.1.27.
Planar lipid bilayer recordings were used to study Ca channels from bovine cardiac sarcolemmal membranes. Ca channel activity was recorded in the absence of nucleotides or soluble enzymes, over a range of membrane potentials and ionic conditions that cannot be achieved in intact cells. The dihydropyridine-sensitive L-type Ca channel, studied in the presence of Bay K 8644, was identified by a detailed comparison of its properties in artificial membranes and in intact cells. L-type Ca channels in bilayers showed voltage dependence of channel activation and inactivation, open and closed times, and single-channel conductances in Ba2+ and Ca2+ very similar to those found in cell-attached patch recordings. Open channels were blocked by micromolar concentrations of external Cd2+. In this cell-free system, channel activity tended to decrease during the course of an experiment, reminiscent of Ca2+ channel "rundown" in whole-cell and excised-patch recordings. A purely voltage-dependent component of inactivation was observed in the absence of Ca2+ stores or changes in intracellular Ca2+. Millimolar internal Ca2+ reduced unitary Ba2+ influx but did not greatly increase the rate or extent of inactivation or the rate of channel rundown. In symmetrical Ba2+ solutions, unitary conductance saturated as the Ba2+ concentration was increased up to 500 mM. The bilayer recordings also revealed activity of a novel Ca2+-permeable channel, termed "B-type" because it may contribute a steady background current at negative membrane potentials, which is distinct from L-type or T-type Ca channels previously reported. Unlike L-type channels, B-type channels have a small unitary Ba2+ conductance (7 pS), but do not discriminate between Ba2+ and Ca2+, show no obvious sensitivity to Bay K 8644, and do not run down. Unlike either L- or T-type channels, B-type channels did not require a depolarization for activation and displayed mean open times of greater than 100 ms.
采用平面脂质双层记录法研究牛心肌肌膜上的钙通道。在不存在核苷酸或可溶性酶的情况下,于一系列完整细胞无法实现的膜电位和离子条件下记录钙通道活性。在存在Bay K 8644的情况下研究的二氢吡啶敏感性L型钙通道,通过详细比较其在人工膜和完整细胞中的特性得以鉴定。双层膜中的L型钙通道在通道激活和失活、开放和关闭时间以及Ba2+和Ca2+中的单通道电导方面表现出的电压依赖性,与在细胞贴附式膜片钳记录中发现的非常相似。开放通道被微摩尔浓度的外部Cd2+阻断。在这个无细胞系统中,通道活性在实验过程中往往会降低,这与全细胞和膜片切除记录中的钙通道“衰减”现象相似。在不存在钙库或细胞内钙变化的情况下,观察到了一种纯粹的电压依赖性失活成分。毫摩尔浓度的细胞内钙减少了单一Ba2+内流,但并没有显著增加失活的速率或程度,也没有增加通道衰减的速率。在对称的Ba2+溶液中,随着Ba2+浓度增加到500 mM,单通道电导达到饱和。双层记录还揭示了一种新型钙通透通道的活性,因其可能在负膜电位下贡献稳定的背景电流而被称为“B型”,它与先前报道的L型或T型钙通道不同。与L型通道不同,B型通道的单一Ba2+电导较小(7 pS),但对Ba2+和Ca2+没有选择性,对Bay K 8644没有明显敏感性,并且不会衰减。与L型或T型通道都不同,B型通道激活不需要去极化,平均开放时间大于100毫秒。