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Effects of unsaturated fatty acids on the kinetics of voltage-gated proton channels heterologously expressed in cultured cells

机译:不饱和脂肪酸对培养细胞中异源表达的电压门控质子通道动力学的影响

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摘要

Unsaturated fatty acids are key components of the biological membranes of all cells, and precursors of mediators for cell signalling. Arachidonic acid (AA) is an unsaturated fatty acid known to modulate the activities of various ion channels, including the voltage-gated proton (Hv) channel, which supports the rapid production of reactive oxygen species (ROS) in phagocytes through regulation of pH and membrane potential. However, the molecular mechanisms and physiological functions of the effects of AA on Hv channels remain unclear. In the present study, we report an electrophysiological analysis of the effects of AA on the mouse Hv channel (mHv1) heterologously expressed in HEK293T cells. Application of AA to excised inside-out patch membranes rapidly induced a robust increase in the amplitude of the proton current through mHv1. The current increase was accompanied by accelerated activation kinetics and a small leftward shift of the current-voltage relationship. In monomeric channels lacking the coiled-coil region of the channel protein, the shift in the current-voltage relationship was diminished but activation and deactivation remained accelerated. Studies with several AA derivatives showed that double bonds and hydrophilic head groups are essential for the effect of AA, although charge was not important. The application of phospholipase A(2) (PLA(2)), which generates AA from cell membrane phospholipids, stimulated mHv1 activity to a similar extent as direct application of approximate to 20m AA, suggesting that endogenous AA may regulate Hv channel activity.
机译:不饱和脂肪酸是所有细胞生物膜的关键成分,也是细胞信号传导介质的前体。花生四烯酸(AA)是一种不饱和脂肪酸,已知可调节各种离子通道(包括电压门控质子(Hv)通道)的活性,该通道可通过调节pH和pH来支持吞噬细胞中活性氧(ROS)的快速产生。膜电位。然而,AA对Hv通道的影响的分子机制和生理功能仍不清楚。在本研究中,我们报告了AA对HEK293T细胞中异源表达的小鼠Hv通道(mHv1)的影响的电生理分析。将AA应用于从内而外切下的贴膜可迅速引起通过mHv1的质子电流幅度的强劲增长。电流增加伴随着加速的活化动力学和电流-电压关系的小左移。在缺少通道蛋白的卷曲螺旋区域的单体通道中,电流-电压关系的偏移减小了,但活化和失活仍在加速。对几种AA衍生物的研究表明,双键和亲水性头基对于AA的作用至关重要,尽管电荷并不重要。从细胞膜磷脂产生AA的磷脂酶A(2)(PLA(2))的应用刺激mHv1活性达到与直接应用约20m AA相似的程度,表明内源性AA可能调节Hv通道活性。

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