Chen Y H, DeHaan R L
Department of Anatomy and Cell Biology, Emory University Health Science Center, Atlanta, Georgia 30322.
J Membr Biol. 1992 Apr;127(2):95-111. doi: 10.1007/BF00233282.
We used the double whole-cell voltage-clamp technique on ventricle cell pairs isolated from 7-day chick heart to measure the conductance of their gap junctions (Gj) and junctional channels (gamma j) with a steady-state voltage difference (Vj) applied across the junction. Currents were recorded from single gap junction channels (ij) as symmetrical rectangular signals of equal size and opposite sign in the two cells, and gamma j was measured from ij/Vj. We observed channel openings at six reproducible conductance levels with means of 42.6, 80.7, 119.6, 157.7, 200.4 and 240.3 pS. More than half of all openings were to the 80- and 160-pS conductance levels. The probability that a high conductance event (e.g., 160 or 240 pS) results from the random simultaneous opening of several 40-pS channels is small, based on their frequency of occurrence and on the prevalence of shifts between small and large conductance states with no intervening 40-pS steps. Our results are consistent with three models of embryonic cardiac gap junction channel configuration: a homogeneous population of 40-pS channels that can open cooperatively in groups of up to six; a single population of large channels with a maximal conductance near 240 pS and five smaller substates; or several different channel types, each with its own conductance. Gj was determined from the junctional current (Ij) elicited by rectangular pulses of applied transjunctional voltage as Ij/Vj. It was highest near 0 Vj and was progressively reduced by application of Vj between 20 and 80 mV or -20 and -80 mV. In response to increases in Vj, Gj decayed in a voltage- and time-dependent fashion. After a 6-sec holding period at 0 Vj, the initial conductance (G(init) measured immediately after the onset of an 80-mV step in Vj was nearly the same as that measured by a 10-mV prepulse. However, during 6-sec pulses of Vj greater than +/- 20 mV, Gj declined over several seconds from G(init)to a steady-state value (Gss). At potentials greater than +/- 20 mV the current decay could be fit with biexponential curves with the slow decay time constant (tau 2) 5-20 times longer than tau 1. For the response to a step to 80 mV Vj, for example, tau 1 = 127 msec and tau 2 = 2.6 sec. The rate of current decay in response to smaller positive or negative steps in Vj was slower, the magnitude of the decline was smaller, and the ratio tau 2/tau 1 decreased.(ABSTRACT TRUNCATED AT 400 WORDS)
我们采用双全细胞膜电压钳技术,对从7日龄鸡心脏分离的心室细胞对进行研究,通过在连接处施加稳态电压差(Vj)来测量其缝隙连接(Gj)和连接通道(γj)的电导。从单个缝隙连接通道记录电流(ij),其在两个细胞中表现为大小相等、方向相反的对称矩形信号,γj通过ij/Vj来测量。我们观察到通道开口处于六个可重复的电导水平,平均值分别为42.6、80.7、119.6、157.7、200.4和240.3 pS。超过一半的开口处于80 - 160 pS的电导水平。基于高电导事件(例如160或240 pS)的发生频率以及大小电导状态之间不存在中间40 - pS步长的转换情况,由几个40 - pS通道随机同时打开导致高电导事件的可能性很小。我们的结果与胚胎心脏缝隙连接通道构型的三种模型一致:由多达六个可协同打开的40 - pS通道组成的同质群体;最大电导接近240 pS且有五个较小亚状态的单个大通道群体;或几种不同的通道类型,每种具有其自身的电导。Gj通过施加跨连接电压的矩形脉冲引发的连接电流(Ij),按照Ij/Vj来确定。它在Vj接近0时最高,当在20至80 mV或 - 20至 - 80 mV之间施加Vj时逐渐降低。响应Vj的增加,Gj以电压和时间依赖性方式衰减。在0 Vj下保持6秒后,Vj阶跃80 mV开始后立即测量的初始电导(G(init))与通过10 mV预脉冲测量的初始电导几乎相同。然而,在Vj大于+/- 20 mV的6秒脉冲期间,Gj在几秒钟内从G(init)下降到稳态值(Gss)。在大于+/- 20 mV的电位下,电流衰减可用双指数曲线拟合,慢衰减时间常数(tau 2)比tau 1长5 - 20倍。例如,对于80 mV Vj的阶跃响应,tau 1 = 127毫秒,tau 2 = 2.6秒。响应Vj较小的正向或负向阶跃时电流衰减速率较慢,下降幅度较小,且tau 2/tau 1比值减小。(摘要截断于400字)