Crosstalk between cholesterol and PIP2 in the regulation of Kv7.2/Kv7.3 channels.

IF 2.9 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biological Chemistry Pub Date : 2023-08-08 Print Date: 2024-03-25 DOI:10.1515/hsz-2023-0204
Mayra Delgado-Ramírez, Ana Laura López-Serrano, Sergio Sánchez-Armass, Ulises Meza, Aldo A Rodríguez-Menchaca
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Abstract

The activity of neuronal Kv7.2/Kv7.3 channels is critically dependent on PIP2 and finely modulated by cholesterol. Here, we report the crosstalk between cholesterol and PIP2 in the regulation of Kv7.2/Kv7.3 channels. Our results show that currents passing through Kv7.2/Kv7.3 channels in cholesterol-depleted cells, by acute application of methyl-β-cyclodextrin (MβCD), were less sensitive to PIP2 dephosphorylation strategies than those of control cells, suggesting that cholesterol depletion enhances the Kv7.2/Kv7.3-PIP2 interaction. In contrast, the sensitivity of Kv7.2/Kv7.3 channels to acute membrane cholesterol depletion by MβCD was not altered in mutant channels with different apparent affinities for PIP2.

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胆固醇和 PIP2 在调控 Kv7.2/Kv7.3 通道中的相互作用
神经元 Kv7.2/Kv7.3 通道的活性严重依赖于 PIP2,并受胆固醇的精细调节。在这里,我们报告了胆固醇和 PIP2 在调控 Kv7.2/Kv7.3 通道过程中的相互影响。我们的研究结果表明,通过急性应用甲基-β-环糊精(MβCD),胆固醇耗竭细胞中通过 Kv7.2/Kv7.3 通道的电流对 PIP2 去磷酸化策略的敏感性低于对照细胞,这表明胆固醇耗竭增强了 Kv7.2/Kv7.3-PIP2 的相互作用。与此相反,在对 PIP2 有不同表观亲和力的突变通道中,Kv7.2/Kv7.3 通道对通过 MβCD 进行急性膜胆固醇耗竭的敏感性没有改变。
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来源期刊
Biological Chemistry
Biological Chemistry 生物-生化与分子生物学
CiteScore
7.20
自引率
0.00%
发文量
63
审稿时长
4-8 weeks
期刊介绍: Biological Chemistry keeps you up-to-date with all new developments in the molecular life sciences. In addition to original research reports, authoritative reviews written by leading researchers in the field keep you informed about the latest advances in the molecular life sciences. Rapid, yet rigorous reviewing ensures fast access to recent research results of exceptional significance in the biological sciences. Papers are published in a "Just Accepted" format within approx.72 hours of acceptance.
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