Suppr超能文献

BK-VEDEC 剪接变异体形成的线粒体大电导钾通道的单通道特性。

Single channel properties of mitochondrial large conductance potassium channel formed by BK-VEDEC splice variant.

机构信息

Laboratory of Intracellular Ion Channels, Nencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur St., 02-093, Warsaw, Poland.

Department of Physics and Biophysics, Institute of Biology, Warsaw, University of Life Sciences-SGGW, Nowoursynowska 166, 02-787, Warsaw, Poland.

出版信息

Sci Rep. 2021 May 25;11(1):10925. doi: 10.1038/s41598-021-90465-3.

Abstract

The activation of mitochondrial large conductance calcium-activated potassium (mitoBK) channels increases cell survival during ischemia/reperfusion injury of cardiac cells. The basic biophysical and pharmacological properties of mitoBK correspond to the properties of the BK channels from the plasma membrane. It has been suggested that the VEDEC splice variant of the KCNMA1 gene product encoding plasma membrane BK is targeted toward mitochondria. However there has been no direct evidence that this protein forms a functional channel in mitochondria. In our study, we used HEK293T cells to express the VEDEC splice variant and observed channel activity in mitochondria using the mitoplast patch-clamp technique. For the first time, we found that transient expression with the VEDEC isoform resulted in channel activity with the conductance of 290 ± 3 pS. The channel was voltage-dependent and activated by calcium ions. Moreover, the activity of the channel was stimulated by the potassium channel opener NS11021 and inhibited by hemin and paxilline, which are known BK channel blockers. Immunofluorescence experiments confirmed the partial colocalization of the channel within the mitochondria. From these results, we conclude that the VEDEC isoform of the BK channel forms a functional channel in the inner mitochondrial membrane. Additionally, our data show that HEK293T cells are a promising experimental model for expression and electrophysiological studies of mitochondrial potassium channels.

摘要

线粒体大电导钙激活钾(mitoBK)通道的激活可增加心肌细胞缺血/再灌注损伤期间的细胞存活率。mitoBK 的基本生物物理和药理学特性与质膜 BK 通道的特性相对应。有人提出,编码质膜 BK 的 KCNMA1 基因产物的 VEDEC 剪接变体被靶向线粒体。然而,尚无直接证据表明该蛋白在线粒体中形成功能性通道。在我们的研究中,我们使用 HEK293T 细胞表达 VEDEC 剪接变体,并使用线粒体Mitoplast 膜片钳技术观察线粒体中的通道活性。我们首次发现,瞬时表达 VEDEC 同工型可导致具有 290 ± 3 pS 电导的通道活性。该通道对电压具有依赖性,并被钙离子激活。此外,钾通道 opener NS11021 可刺激通道活性,血红素和 paxilline 抑制通道活性,血红素和 paxilline 是已知的 BK 通道阻断剂。免疫荧光实验证实了通道在线粒体内部的部分共定位。根据这些结果,我们得出结论,BK 通道的 VEDEC 同工型在内线粒体膜中形成功能性通道。此外,我们的数据表明,HEK293T 细胞是表达和研究线粒体钾通道的电生理学的有前途的实验模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d4b/8149700/c89a0063c596/41598_2021_90465_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验