Stimers J R, Shigeto N, Lieberman M
Department of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710.
J Gen Physiol. 1990 Jan;95(1):61-76. doi: 10.1085/jgp.95.1.61.
Spontaneously beating aggregates of cultured embryonic chick cardiac myocytes, maintained at 37 degrees C, were voltage clamped using a single microelectrode switching clamp to measure the current generated by the Na/K pump (Ip). In resting, steady-state preparations an ouabain-sensitive current of 0.46 +/- 0.03 microA/cm2 (n = 22) was identified. This current was not affected by 1 mM Ba, which was used to reduce inward rectifier current (IK1) and linearize the current-voltage relationship. When K-free solution was used to block Ip, subsequent addition of Ko reactivated the Na/K pump, generating an outward reactivation current that was also ouabain sensitive. The reactivation current magnitude was a saturating function of Ko with a Hill coefficient of 1.7 and K0.5 of 1.9 mM in the presence of 144 mM Nao. The reactivation current was increased in magnitude when Nai was increased by lengthening the period of time that the preparation was exposed to K-free solution prior to reactivation. When Nai was raised by 3 microM monensin, steady-state Ip was increased more than threefold above the resting value to 1.74 +/- 0.09 microA/cm2 (n = 11). From these measurements and other published data we calculate that in a resting myocyte: (a) the steady-state Ip should hyperpolarize the membrane by 6.5 mV, (b) the turnover rate of the Na/K pump is 29 s-1, and (c) the Na influx is 14.3 pmol/cm2.s. We conclude that in cultured embryonic chick cardiac myocytes, the Na/K pump generates a measurable current which, under certain conditions, can be isolated from other membrane currents and has properties similar to those reported for adult cardiac cells.
将培养的鸡胚心肌细胞聚集体维持在37℃,这些聚集体能自发搏动,使用单微电极切换钳对其进行电压钳制,以测量钠钾泵产生的电流(Ip)。在静息、稳态制剂中,鉴定出哇巴因敏感电流为0.46±0.03微安/平方厘米(n = 22)。该电流不受1毫摩尔/升钡的影响,钡用于降低内向整流电流(IK1)并使电流-电压关系线性化。当使用无钾溶液阻断Ip时,随后添加钾可重新激活钠钾泵,产生外向再激活电流,该电流也对哇巴因敏感。在144毫摩尔/升钠离子存在的情况下,再激活电流大小是钾离子的饱和函数,希尔系数为1.7,半最大激活浓度(K0.5)为1.9毫摩尔/升。当在再激活前通过延长制剂暴露于无钾溶液的时间来增加细胞内钠离子(Nai)时,再激活电流大小增加。当通过3微摩尔莫能菌素使Nai升高时,稳态Ip比静息值增加三倍以上,达到1.74±0.09微安/平方厘米(n = 11)。根据这些测量结果和其他已发表的数据,我们计算出在静息心肌细胞中:(a)稳态Ip应使膜超极化6.5毫伏,(b)钠钾泵的周转速率为29次/秒,(c)钠内流为14.3皮摩尔/平方厘米·秒。我们得出结论,在培养的鸡胚心肌细胞中,钠钾泵产生可测量的电流,在某些条件下,该电流可与其他膜电流分离,并且具有与成年心脏细胞报道的特性相似的性质。