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The Drosophila tweety family: molecular candidates for large-conductance Ca2+-activated Cl- channels.

机译:果蝇tweety家族:大电导Ca2 +激活的Cl-通道的分子候选物。

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Calcium-activated chloride currents (I(Cl(Ca))) can be recorded in almost all cells, but the molecular identity of the channels underlying this Cl- conductance is still incompletely understood. Here, I report that tweety, a gene located in Drosophila flightless, possesses five or six transmembrane segments, and that a human homologue of tweety (hTTYH3) is a novel large-conductance Ca2+-activated Cl- channel, while the related gene, hTTYH1, is a swelling-activated Cl- current. hTTYH3 is expressed in excitable tissues, including the heart, brain and skeletal muscle, whereas hTTYH1 is expressed mainly in the brain. Expression of hTTYH3 in CHO cells generated a unique Cl- current activated by an increase in the intracellular Ca2+ concentration. The hTTYH3-induced Cl- current had a linear current-voltage (I-V) relationship, a large single-channel conductance (260 pS) and the anion permeability sequence I- > Br- > Cl-. Like native Ca2+-activated Cl- channels, the hTTYH3 channel showed complex gating kineticsand voltage-dependent inactivation, and was dependent on micromolar intracellular Ca2+ concentration. Expression in CHO cells of an hTTYH1 splice variant that lacks the C-terminal glutamate-rich domain of hTTYH1 (hTTYH1sv) generated a swelling-activated Cl- current. I conclude that investigation of the tweety family will provide important information about large-conductance Cl- channel molecules.
机译:几乎在所有细胞中都可以记录钙激活的氯离子电流(I(Cl(Ca))),但仍无法完全了解这种Cl电导的通道的分子身份。在这里,我报道tweety,一个位于果蝇不飞行的基因,具有五个或六个跨膜区段,并且人类tweety的同源物(hTTYH3)是一种新型的大电导Ca2 +激活的Cl-通道,而相关基因hTTYH1 ,是溶胀激活的Cl电流。 hTTYH3在可兴奋的组织中表达,包括心脏,大脑和骨骼肌,而hTTYH1主要在大脑中表达。 hTTYH3在CHO细胞中的表达产生了独特的Cl-电流,该电流被细胞内Ca2 +浓度的增加激活。 hTTYH3诱导的Cl-电流具有线性电流-电压(I-V)关系,较大的单通道电导(260 pS)和阴离子渗透率序列I-> Br-> Cl-。像天然Ca2 +激活的Cl-通道一样,hTTYH3通道显示出复杂的门控动力学和电压依赖性失活,并且依赖于微摩尔细胞内Ca2 +浓度。缺少hTTYH1(hTTYH1sv)富含C端谷氨酸结构域的hTTYH1剪接变体在CHO细胞中的表达产生了溶胀激活的C1电流。我得出结论,对二十族的研究将提供有关大电导Cl通道分子的重要信息。

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