Hurnák O, Zachar J
Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava.
Gen Physiol Biophys. 1994 Jun;13(3):171-92.
Large-conductance chloride channels (maxi-Cl channels) were studied in cultured myoblasts (L6 rat muscle cell line); in excised (inside-out) and in cell attached membrane patches using a conventional patch clamp method. The incidence of maxi-Cl channels was substantially higher in proliferating myoballs, then in quiescent (bottom-attached) myoblasts (90% and 50% percent of examined cells, respectively). The maxi-Cl channels in myoballs were present both in cell attached and excised patches. The channel conductance at symmetric [Cl] = 150 mmol/l was 359 +/- 42 pS (n = 74) in quiescent cells and 439 +/- 10 pS (n = 6) in proliferating myoballs respectively. The conductance of the channel in quiescent cells increased with chloride concentration in symmetric NaCl rich solutions according to Michaelis-Menten curve with the saturation limiting conductance of about 640 pS (gmax) and Km = 112 mmol/l. The shift of the reversal potential upon increasing the pipette concentration of NaCl from 150 to 250 mmol/l was consistent with PNa/PCl = 0.1. Neither the conductance nor the activation of the channel were dependent on the presence of calcium ions. The bell-shaped steady state channel conductance-voltage relationship is asymmetric and can be fitted by two Boltzmann equations with different Vh and k constants; -25.6 mV and -6.8 mV, respectively, for the negative side and +49.6 mV and +13.7 mV for the positive side in quiescent cells. The corresponding values in proliferating myoballs were as follows: -15.5 mV and -2.4 mV, respectively, for the negative side and +31.4 mV and +6.8 mV for the positive side. From the maximum slopes of the Popen versus V curves an estimate was made of the charges for the gates that close at negative (3.5) or positive (1.7) potentials, respectively, in quiescent cells. The corresponding values in myoballs were 10.6 and 3.7, respectively. The probability of one gate to be open was dependent on the state of activation of the opposite gate as determined by prepulses of the opposite polarity. The channel showed multiple (up to six) conductance levels that may develop in a step-like manner. The onset of the full-grown maxi-Cl channel is fairly abrupt; it might, however, be preceded by a small conductance unit activity. It is supposed that the differences between the quiescent myoblasts and proliferating myoballs might reflect increased expression of maxi-Cl channels in myoballs to perform as yet unknown role in the cell cycle and/or proliferation of the myoblasts.
在培养的成肌细胞(L6大鼠肌肉细胞系)中,采用传统的膜片钳方法,对大电导氯离子通道(maxi-Cl通道)进行了研究,研究对象包括切除膜片(内面向外)和细胞贴附膜片。maxi-Cl通道在增殖的肌球中的发生率显著高于静止(底部附着)的成肌细胞(分别为所检测细胞的90%和50%)。肌球中的maxi-Cl通道在细胞贴附膜片和切除膜片中均有存在。在对称[Cl] = 150 mmol/L时,静止细胞中的通道电导为359 +/- 42 pS(n = 74),增殖肌球中的通道电导为439 +/- 10 pS(n = 6)。在富含对称NaCl的溶液中,静止细胞中通道的电导随氯离子浓度的增加而根据米氏曲线增加,饱和极限电导约为640 pS(gmax),Km = 112 mmol/L。当移液器中NaCl浓度从150 mmol/L增加到250 mmol/L时,反转电位的变化与PNa/PCl = 0.1一致。通道的电导和激活均不依赖于钙离子的存在。钟形的稳态通道电导-电压关系是不对称的,可以用两个具有不同Vh和k常数的玻尔兹曼方程拟合;在静止细胞中,负侧分别为-25.6 mV和-6.8 mV,正侧分别为+49.6 mV和+13.7 mV。增殖肌球中的相应值如下:负侧分别为-15.5 mV和-2.4 mV,正侧分别为+31.4 mV和+6.8 mV。根据Popen与V曲线的最大斜率,估计了在静止细胞中分别在负(3.5)或正(1.7)电位关闭的门的电荷量。肌球中的相应值分别为10.6和3.7。一个门打开的概率取决于相反极性预脉冲所确定的相反门的激活状态。该通道显示出多个(多达六个)电导水平,可能以阶梯状方式发展。成熟的maxi-Cl通道的起始相当突然;然而,在此之前可能有一个小电导单位的活动。据推测,静止成肌细胞和增殖肌球之间的差异可能反映了肌球中maxi-Cl通道表达的增加,以在成肌细胞的细胞周期和/或增殖中发挥尚未明确的作用。