首页> 外文期刊>The Journal of Membrane Biology: An International Journal for Studies on the Structure, Function & Genesis of Biomembranes >Comparison of voltage-activated Cl- channels in rat parotid acinar cells with ClC-2 in a mammalian expression system.
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Comparison of voltage-activated Cl- channels in rat parotid acinar cells with ClC-2 in a mammalian expression system.

机译:在哺乳动物表达系统中,大鼠腮腺腺泡细胞中的电压激活的Cl-通道与ClC-2的比较。

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Rat parotid acinar cells express Cl- currents that are activated in a time-dependent manner by hyperpolarized potentials. ClC-2, a member of the ClC gene family, codes for a voltage-gated, inward rectifying anion channel when expressed in Xenopus oocytes. In the present study, we found that cDNA derived from individual parotid acinar cells contained sequence identical to that reported for ClC-2 in rat brain and heart. A polyclonal antibody generated against the N-terminal cytoplasmic domain of ClC-2 recognized an approximately 100 kD protein on western blots of both brain and parotid gland. ClC-2 expressed in oocytes has different kinetics from the currents found in parotid acinar cells. Since the ClC-2 channel was cloned from and its transcripts are expressed in mammalian tissue, we compared the channel properties of acinar cells to a mammalian expression system. We expressed ClC-2 channels in human embryonic kidney cells, HEK 293, using recombinant ClC-2 DNA and ClC-2 DNA fused with DNA coding for jellyfish green fluorescent protein (GFP). Confocal microscopy revealed that the expressed ClC-2-GFP chimera protein localized to the plasma membrane. Whole cell Cl- currents from HEK 293 cells expressing ClC-2-GFP were similar, if not identical, to the Cl- currents recorded from cells transfected with ClC-2 cDNA (no GFP). The voltage-dependence and kinetics of ClC-2 channels expressed in HEK 293 cells were quite similar to those in acinar cells. Channels in parotid acinar and HEK 293 cells activated at more positive membrane potentials and with a faster time course than the channels expressed in Xenopus oocytes. In summary, we found that ClC-2 message and protein are expressed in salivary cells and that the properties of voltage-activated, inward rectifying Cl- channels in acinar cells are similar to those generated by the ClC-2-GFP construct expressed in HEK 293 cells. The properties of the ClC-2 anion channel seem to be dependent on the type of cell background in which it is expressed.
机译:大鼠腮腺腺泡细胞表达Cl-电流,Cl-电流通过时间被超极化电位激活。 ClC-2是ClC基因家族的成员,当在非洲爪蟾卵母细胞中表达时,编码一个电压门控,向内整流的阴离子通道。在本研究中,我们发现源自单个腮腺腺泡细胞的cDNA含有与大鼠脑和心脏中ClC-2报道的序列相同的序列。针对ClC-2的N端胞质结构域产生的多克隆抗体在大脑和腮腺的Western印迹上识别了大约100 kD的蛋白质。在卵母细胞中表达的ClC-2与腮腺腺泡细胞中的电流具有不同的动力学。由于从中克隆了ClC-2通道并在哺乳动物组织中表达了其转录本,因此我们比较了腺泡细胞与哺乳动物表达系统的通道特性。我们使用与编码水母绿色荧光蛋白(GFP)的DNA融合的重组ClC-2 DNA和ClC-2 DNA在人类胚胎肾细胞HEK 293中表达了ClC-2通道。共聚焦显微镜显示,表达的ClC-2-GFP嵌合蛋白定位于质膜。来自表达ClC-2-GFP的HEK 293细胞的全细胞Cl-电流与从ClC-2 cDNA(无GFP)转染的细胞记录的Cl-电流相似,如果不是相同的话。 HEK 293细胞中表达的ClC-2通道的电压依赖性和动力学与腺泡细胞中的相似。与爪蟾卵母细胞中表达的通道相比,腮腺腺泡和HEK 293细胞中的通道以更高的阳性膜电位和更快的时程激活。总之,我们发现ClC-2信息和蛋白质在唾液细胞中表达,并且腺泡细胞中电压激活的,向内整流的Cl-通道的性质与HEK中表达的ClC-2-GFP构建物相似293个细胞。 ClC-2阴离子通道的性质似乎取决于表达它的细胞背景的类型。

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