Kettenmann H, Orkand R K, Lux H D
Pflugers Arch. 1984 Mar;400(3):215-21. doi: 10.1007/BF00581550.
K+ channels were studied in oligodendrocytes in cultures of mouse spinal cord. Single channel currents were measured using the gigaseal technique. The conductance of the channels varied greatly i.e. from 6 to 125 pS (38 +/- 28 SD, N = 21). In some patches there were up to three current levels of the same size. At -70 mV the open state probability was 0.51 +/- 0.17 and the average duration of an opening 70 +/- 20 ms for 4 channels with conductance from 16-57 pS. These analyses exclude brief flickering (less than 2 ms) or long closed periods (seconds to minutes). These times were not markedly affected by pulling the patch off the cell or by superfusing the isolated patch with media containing 10 mmol X 1(-1) TEA or EGTA without Ca2+. At membrane potentials between -90 and -30 mV there was a small but consistent effect of depolarization to increase the open state probability. Large positive or negative voltage steps decreased the open state probability. Current voltage measurements on intact cells showed a striking decrease in membrane conductance at these large membrane potentials. The leakage conductance of the patch also exhibited some K+ selectivity. The oligodendrocyte membrane appears to contain about one K+ channel per 5 micron 2. The known electrical properties of cultured oligodendrocytes can essentially be explained by the distribution and properties of these K+ channels.
在小鼠脊髓培养物中的少突胶质细胞中研究了钾离子通道。使用千兆封接技术测量单通道电流。通道的电导变化很大,即从6到125皮西门子(38±28标准差,N = 21)。在一些膜片中,存在多达三个相同大小的电流水平。在-70毫伏时,对于4个电导为16 - 57皮西门子的通道,开放状态概率为0.51±0.17,平均开放持续时间为70±20毫秒。这些分析排除了短暂闪烁(小于2毫秒)或长时间关闭期(数秒至数分钟)。将膜片从细胞上拉开或用含有10毫摩尔×1(-1)四乙铵或无钙离子的乙二醇双四乙酸的培养基灌流分离的膜片,这些时间没有明显受到影响。在-90至-30毫伏之间的膜电位下,去极化有一个小但一致的效应,可增加开放状态概率。大的正电压或负电压阶跃会降低开放状态概率。对完整细胞的电流 - 电压测量显示,在这些大膜电位下膜电导显著降低。膜片的漏电导也表现出一定的钾离子选择性。少突胶质细胞膜似乎每5微米2含有约一个钾离子通道。培养的少突胶质细胞的已知电特性基本上可以由这些钾离子通道的分布和特性来解释。