Rousseau E, Michaud C, Lefebvre D, Proteau S, Decrouy A
Department of Physiology and Biophysics, University of Sherbrooke, Québec J1H 5N4, Canada.
Biophys J. 1996 Feb;70(2):703-14. doi: 10.1016/S0006-3495(96)79610-8.
Recent reports suggest that the nuclear envelope possesses specific ion transport mechanisms that regulate the electrolyte concentrations within the nucleoplasm and perinuclear space. In this work, intact nuclei were isolated from sheep cardiac cells. After chromatin digestion, the nuclear envelopes were sonicated and four nuclear vesicle populations were separated by sucrose step gradients (SF1-SF4). These fractions were compared by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and their protein content was analyzed by Western blot, using lamin and SEC 61 antibodies. The lamins, which are associated with the inner nuclear membrane, were present in three fractions, SF2, SF3, and SF4, with a lower amount in SF2. The SEC 61 protein, a marker of the rough endoplasmic reticulum, was detected in small amounts in SF1 and SF2. Upon fusion of vesicles into bilayers, the activities of nuclear ionic channels were recorded in 50 mM trans/250 mM cis KCl or CsCl, pH 7.2. Two types of Cl- selective channels were recorded: a large conducting 150-180-pS channel displaying substates, and a low conducting channel of 30 pS. They were both spontaneously active into bilayers, and their open probability was poorly voltage dependent at negative voltages. Retinoic acid (10(-8) M) increases the po of the large Cl- conducting channel, whereas ATP modifies the kinetics of the low conductance anion selective channel. Our data also suggest that this anionic channel is mainly present in the SF3 and SF4 population. The presence of a 181 +/- 10 pS cation-selective channel was consistently observed in the SF2 population. The behavior of this channel was voltage dependent in the voltage range -80 to +60 mV. Furthermore, we report for the first time the activity of a channel exclusively present in the SF3 and SF4 fractions, shown to contain mainly inner membrane vesicles. This cation selective channel displays a 75-pS conductance in 50 mM trans/250 mM cis K-gluconate. It is concluded that the bilayer reconstitution technique is an attractive approach to studying the electrophysiological properties of the inner and outer membranes of the nuclear envelope.
最近的报道表明,核膜拥有特定的离子转运机制,可调节核质和核周空间内的电解质浓度。在这项研究中,从绵羊心脏细胞中分离出完整的细胞核。染色质消化后,对核膜进行超声处理,并通过蔗糖阶梯梯度(SF1 - SF4)分离出四个核囊泡群体。通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳对这些组分进行比较,并使用核纤层蛋白和SEC 61抗体通过蛋白质印迹分析它们的蛋白质含量。与内核膜相关的核纤层蛋白存在于三个组分SF2、SF3和SF4中,SF2中的含量较低。粗糙内质网的标志物SEC 61蛋白在SF1和SF2中少量检测到。当囊泡融合成双层膜时,在50 mM反式/250 mM顺式KCl或CsCl、pH 7.2条件下记录核离子通道的活性。记录到两种类型的Cl-选择性通道:一种是具有亚状态的大电导150 - 180 pS通道,另一种是30 pS的低电导通道。它们在双层膜中都是自发活动的,并且在负电压下其开放概率对电压的依赖性较弱。视黄酸(10(-8) M)增加了大Cl-传导通道的开放概率,而ATP改变了低电导阴离子选择性通道的动力学。我们的数据还表明,这种阴离子通道主要存在于SF3和SF4群体中。在SF2群体中始终观察到一个181±10 pS的阳离子选择性通道。该通道的行为在-80至+60 mV的电压范围内依赖于电压。此外,我们首次报道了仅存在于SF3和SF4组分中的一种通道的活性,这些组分显示主要包含内膜囊泡。这种阳离子选择性通道在50 mM反式/250 mM顺式葡萄糖酸钾中显示出75 pS的电导。结论是,双层膜重建技术是研究核膜内膜和外膜电生理特性的一种有吸引力的方法。