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乙醇通过降低 Kv7.2 亚基对 PI(4,5)P2 的敏感性来抑制 Kv7.2/7.3 通道的开放概率。

Ethanol inhibits Kv7.2/7.3 channel open probability by reducing the PI(4,5)P2 sensitivity of Kv7.2 subunit.

机构信息

Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea.

出版信息

BMB Rep. 2021 Jun;54(6):311-316. doi: 10.5483/BMBRep.2021.54.6.231.

DOI:10.5483/BMBRep.2021.54.6.231
PMID:33408002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8249878/
Abstract

Ethanol often causes critical health problems by altering the neuronal activities of the central and peripheral nerve systems. One of the cellular targets of ethanol is the plasma membrane proteins including ion channels and receptors. Recently, we reported that ethanol elevates membrane excitability in sympathetic neurons by inhibiting Kv7.2/7.3 channels in a cell type-specific manner. Even though our studies revealed that the inhibitory effects of ethanol on the Kv7.2/7.3 channel was diminished by the increase of plasma membrane phosphatidylinositol 4,5-bisphosphate (PI (4,5)P2), the molecular mechanism of ethanol on Kv7.2/7.3 channel inhibition remains unclear. By investigating the kinetics of Kv7.2/7.3 current in high K+ solution, we found that ethanol inhibited Kv7.2/7.3 channels through a mechanism distinct from that of tetraethylammonium (TEA) which enters into the pore and blocks the gate of the channels. Using a non-stationary noise analysis (NSNA), we demonstrated that the inhibitory effect of ethanol is the result of reduction of open probability (PO) of the Kv7.2/7.3 channel, but not of a single channel current (i) or channel number (N). Finally, ethanol selectively facilitated the kinetics of Kv7.2 current suppression by voltage-sensing phosphatase (VSP)-induced PI(4,5)P2 depletion, while it slowed down Kv7.2 current recovery from the VSP-induced inhibition. Together our results suggest that ethanol regulates neuronal activity through the reduction of open probability and PI(4,5)P2 sensitivity of Kv7.2/7.3 channels. [BMB Reports 2021; 54(6): 311-316].

摘要

乙醇通过改变中枢和外周神经系统的神经元活动经常引起严重的健康问题。乙醇的细胞靶点之一是包括离子通道和受体在内的质膜蛋白。最近,我们报道乙醇通过以细胞类型特异性的方式抑制 Kv7.2/7.3 通道来提高交感神经元的膜兴奋性。尽管我们的研究表明,乙醇对 Kv7.2/7.3 通道的抑制作用随着质膜磷脂酰肌醇 4,5-二磷酸(PI(4,5)P2)的增加而减弱,但乙醇对 Kv7.2/7.3 通道抑制的分子机制仍不清楚。通过研究高 K+溶液中 Kv7.2/7.3 电流的动力学,我们发现乙醇通过不同于四乙铵(TEA)的机制抑制 Kv7.2/7.3 通道,TEA 进入孔并阻断通道的门。使用非稳态噪声分析(NSNA),我们证明乙醇的抑制作用是 Kv7.2/7.3 通道开放概率(PO)降低的结果,而不是单个通道电流(i)或通道数(N)的降低。最后,乙醇选择性地促进了电压感应磷酸酶(VSP)诱导的 PI(4,5)P2 耗竭对 Kv7.2 电流抑制的动力学,而减缓了 Kv7.2 电流从 VSP 诱导的抑制中的恢复。总之,我们的结果表明,乙醇通过降低 Kv7.2/7.3 通道的开放概率和 PI(4,5)P2 敏感性来调节神经元活性。[BMB 报告 2021;54(6): 311-316]。

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本文引用的文献

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2
Phosphatidylinositol 4,5-bisphosphate (PIP) regulates KCNQ3 K channels by interacting with four cytoplasmic channel domains.磷脂酰肌醇 4,5-二磷酸(PIP)通过与四个细胞质通道域相互作用来调节 KCNQ3 K 通道。
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细胞内锌通过降低 KCNQ 通道对磷脂酰肌醇 4,5-二磷酸的依赖性来激活它们。
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Effects of acute alcohol on excitability in the CNS.急性酒精对中枢神经系统兴奋性的影响。
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