首页> 美国卫生研究院文献>The Journal of General Physiology >L-type Ca2+ channels access multiple open states to produce two components of Bay K 8644-dependent current in GH3 cells
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L-type Ca2+ channels access multiple open states to produce two components of Bay K 8644-dependent current in GH3 cells

机译:L型Ca2 +通道访问多个打开状态以在GH3细胞中产生依赖Bay K 8644的电流的两个分量

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摘要

To determine the number of L-channel populations responsible for producing the two components of whole-cell L-type Ca2+ channel current revealed by Bay K 8644 (Fass, D.M., and E.S. Levitan. 1996. J. Gen. Physiol. 108:1-11), L-type Ca2+ channel activity was recorded in cell- attached patches. Ensemble tail currents from most (six out of nine) single-channel patches had double-exponential time courses, with time constants that were similar to whole-cell tail current decay values. Also, in single-channel patches subjected to two different levels of depolarization, ensemble tail currents exactly reproduced the voltage dependence of activation of the two whole-cell components: The slow component is activated at more negative potentials than the fast component. In addition, deactivation of Bay K 8644-modified whole-cell L-current was slower after long (100-ms) depolarizations than after short (20-ms) depolarizations, and this phenomenon was also evident in ensemble tail currents from single L-channels. Thus, a single population of L-channels can produce the two components of macroscopic L-current deactivation. To determine how individual L-channels produce multiple macroscopic tail current components, we constructed ensemble tail currents from traces that contained a single opening upon repolarization and no reopenings. These ensemble tails were biexponential. This type of analysis also revealed that reopenings do not contribute to the slowing of tail current deactivation after long depolarizations. Thus, individual L-channels must have access to several open states to produce multiple macroscopic current components. We also obtained evidence that access to these open states can vary over time. Use of several open states may give L-channels the flexibility to participate in many cell functions.
机译:要确定负责产生全细胞L型Ca2 +通道电流的两个分量的L通道种群的数量,Bay K 8644(Fass,DM和ES Levitan。1996. J. Gen. Physiol。108:1 -11),在细胞贴片中记录了L型Ca2 +通道活性。来自大多数(九个中的六个)单通道贴片的集合尾电流具有双指数的时程,其时间常数类似于全细胞尾电流的衰减值。同样,在经受两个不同级别的去极化作用的单通道贴片中,合奏尾电流精确地再现了两个全细胞成分激活的电压依赖性:慢成分在比快成分更多的负电势下被激活。另外,长时间(100-ms)去极化后,Bay K 8644修饰的全细胞L-电流的钝化比短(20-ms)去极化后的钝化慢,这种现象在单个L-电极的整体尾电流中也很明显。渠道。因此,单个L通道种群可以产生宏观L电流失活的两个分量。为了确定各个L通道如何产生多个宏观尾电流分量,我们从包含迹线的迹线构建了集合尾电流,迹线在重新极化时包含一个开口,而没有重新开口。这些合奏的尾巴是双指数的。这种类型的分析还显示,重新开放并不会导致长时间去极化后尾电流失活的放缓。因此,各个L通道必须具有几种打开状态,才能产生多个宏观电流分量。我们还获得了证据,表明对这些开放状态的访问可能会随时间变化。几个打开状态的使用可以使L通道灵活地参与许多单元功能。

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