Kozak J A, Logothetis D E
Department of Physiology and Biophysics, Mount Sinai School of Medicine, C.U.N.Y., NY 10029-6574, USA.
Pflugers Arch. 1997 Apr;433(6):679-90. doi: 10.1007/s004240050332.
Ca(2+)-dependent conductances have been hypothesized to play a role in the bursting pattern of electrical activity of insulin-secreting beta cells in response to high plasma glucose. A Maxi K+ channel has received the most attention, while a low-conductance Ca(2+)-activated K+ current has also been identified. We used an increasingly popular beta cell model system, the beta TC-3 cell line, and the perforated-patch technique to describe the properties of a novel Ca(2+)-dependent Cl- current [ICl(Ca)] in insulin-secreting pancreatic beta cells. The reported ICl(Ca) could be activated under physiological Ca2+ concentrations and is the first of its kind to be described in pancreatic insulin-secreting cells. We found that long depolarizing steps above -20 mV elicited an outward current which showed slow inward relaxation upon repolarization to negative membrane potentials. Both the outward currents and the inward tails showed dependence on Ca2+ influx: their current/voltage (I/V) relations followed that of the "L-like" Ca2+ current (ICa) present in these cells; they were blocked completely by the removal of external Ca2+ or application of Cd2+ at concentrations sufficient for complete block of ICa; and their magnitude increased with the depolarizing step duration. Moreover, the inward tail decayed monoexponentially with a time constant which at voltages negative to activation of ICa showed a weak linear voltage dependence, while at voltages positive to activation of ICa it followed the voltage dependence of ICa. This Ca(2+)-dependent current reversed at -21.5 mV and when the external Cl- concentration was reduced from 159 mM to 62 mM the reversal potential shifted by approximately +20 mV as predicted by the Nernst relation for a Cl(-)-selective current. Cl- channel blockers such as DIDS (100 microM) and niflumic acid (100 microM) blocked this current. We concluded that this current was a Ca(2+)-dependent Cl- current [ICl(Ca)]. From substitution of the external Cl- with various monovalent anions and from the reversal potentials we obtained the following permeability sequence for ICl(Ca): I- > NO3- > Br- > Cl- > Acetate.
钙依赖电导被认为在胰岛素分泌β细胞对高血糖的电活动爆发模式中起作用。大电导钾通道受到了最多关注,同时也鉴定出了一种低电导钙激活钾电流。我们使用了一种越来越受欢迎的β细胞模型系统——βTC - 3细胞系,并采用穿孔膜片钳技术来描述胰岛素分泌胰腺β细胞中一种新型钙依赖氯电流[ICl(Ca)]的特性。所报道的ICl(Ca)可在生理钙浓度下被激活,且是首次在胰腺胰岛素分泌细胞中被描述。我们发现,高于 - 20 mV的长时间去极化步骤会引发外向电流,该电流在复极化至负膜电位时表现出缓慢的内向松弛。外向电流和内向尾电流均显示出对钙内流的依赖性:它们的电流 - 电压(I/V)关系遵循这些细胞中存在的“L型”钙电流(ICa)的关系;通过去除外部钙或应用足以完全阻断ICa的浓度的镉,它们会被完全阻断;并且它们的幅度随去极化步骤持续时间增加。此外,内向尾电流以单指数形式衰减,其时间常数在低于ICa激活电压时表现出较弱的线性电压依赖性,而在高于ICa激活电压时则遵循ICa的电压依赖性。这种钙依赖电流在 - 21.5 mV时反转,当外部氯浓度从159 mM降至62 mM时,反转电位如氯离子选择性电流的能斯特关系所预测的那样大约偏移了 + 20 mV。氯通道阻滞剂如DIDS(100 μM)和氟尼酸(100 μM)可阻断此电流。我们得出结论,该电流是一种钙依赖氯电流[ICl(Ca)]。通过用各种单价阴离子替代外部氯并根据反转电位,我们得到了ICl(Ca)的以下通透性序列:I - > NO3 - > Br - > Cl - > 醋酸根。