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LRRC26是动脉平滑肌细胞中一种功能性BK通道辅助γ亚基。

LRRC26 is a functional BK channel auxiliary γ subunit in arterial smooth muscle cells.

作者信息

Evanson Kirk W, Bannister John P, Leo M Dennis, Jaggar Jonathan H

机构信息

From the Department of Physiology, University of Tennessee Health Science Center, Memphis.

出版信息

Circ Res. 2014 Aug 1;115(4):423-31. doi: 10.1161/CIRCRESAHA.115.303407. Epub 2014 Jun 6.

Abstract

RATIONALE

Smooth muscle cell (myocyte) large-conductance calcium (Ca)(2+)-activated potassium (BK) channels are functionally significant modulators of arterial contractility. Arterial myocytes express both pore-forming BKα and auxiliary β1 subunits, which increase channel Ca(2+) sensitivity. Recently, several leucine-rich repeat containing (LRRC) proteins have been identified as auxiliary γ subunits that elevate the voltage sensitivity of recombinant and prostate adenocarcinoma BK channels. LRRC expression and physiological functions in native cell types are unclear.

OBJECTIVE

Investigate the expression and physiological functions of leucine-rich repeat containing protein 26 (LRRC26) in arterial myocytes.

METHODS AND RESULTS

Reverse transcription polymerase chain reaction and Western blotting detected LRRC26 mRNA and protein in cerebral artery myocytes. Biotinylation, immunofluorescence resonance energy transfer microscopy, and coimmunoprecipitation indicated that LRRC26 was located in close spatial proximity to, and associated with, plasma membrane BKα subunits. LRRC26 knockdown (RNAi) reduced total and surface LRRC26, but did not alter BKα or β1, proteins in arteries. LRRC26 knockdown did not alter Ca(2+) sparks but reduced BK channel voltage sensitivity, which decreased channel apparent Ca(2+) sensitivity and transient BK current frequency and amplitude in myocytes. LRRC26 knockdown also increased myogenic tone over a range (40-100 mm Hg) of intravascular pressures, and reduced vasoconstriction to iberiotoxin and vasodilation to NS1619, BK channel inhibitors and activators, respectively. In contrast, LRRC26 knockdown did not alter depolarization (60 mmol/L K(+))-induced vasoconstriction.

CONCLUSIONS

LRRC26 is expressed, associates with BKα subunits, and elevates channel voltage- and apparent Ca(2+) sensitivity in arterial myocytes to induce vasodilation. This study indicates that arterial myocytes express a functional BK channel γ subunit.

摘要

原理

平滑肌细胞(肌细胞)大电导钙(Ca)(2 +)激活钾(BK)通道是动脉收缩功能的重要调节因子。动脉肌细胞同时表达形成孔道的BKα和辅助β1亚基,这会增加通道对Ca(2 +)的敏感性。最近,几种富含亮氨酸重复序列(LRRC)的蛋白质已被鉴定为辅助γ亚基,可提高重组和前列腺腺癌BK通道的电压敏感性。LRRC在天然细胞类型中的表达及生理功能尚不清楚。

目的

研究富含亮氨酸重复序列蛋白26(LRRC26)在动脉肌细胞中的表达及生理功能。

方法与结果

逆转录聚合酶链反应和蛋白质印迹法检测到脑动脉肌细胞中有LRRC26 mRNA和蛋白质。生物素化、免疫荧光共振能量转移显微镜和免疫共沉淀表明,LRRC26在空间上与质膜BKα亚基紧密相邻并相关联。LRRC26基因敲低(RNA干扰)减少了动脉中总的和表面的LRRC26,但未改变BKα或β1蛋白。LRRC26基因敲低未改变Ca(2 +)火花,但降低了BK通道电压敏感性,这降低了肌细胞中通道的表观Ca(2 +)敏感性以及瞬时BK电流频率和幅度。LRRC26基因敲低还在一定范围(40 - 100 mmHg)的血管内压力下增加了肌源性张力,并分别降低了对iberiotoxin的血管收缩反应和对NS1619的血管舒张反应,iberiotoxin和NS1619分别为BK通道抑制剂和激活剂。相反,LRRC26基因敲低未改变去极化(60 mmol/L K(+))诱导的血管收缩。

结论

LRRC26在动脉肌细胞中表达,与BKα亚基相关联,并提高通道电压和表观Ca(2 +)敏感性以诱导血管舒张。本研究表明动脉肌细胞表达一种功能性BK通道γ亚基。

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本文引用的文献

1
Functional regulation of BK potassium channels by γ1 auxiliary subunits.γ1 辅助亚基对 BK 钾通道功能的调节。
Proc Natl Acad Sci U S A. 2014 Apr 1;111(13):4868-73. doi: 10.1073/pnas.1322123111. Epub 2014 Mar 17.
2
Dynamic regulation of β1 subunit trafficking controls vascular contractility.β1 亚基转运的动态调节控制血管收缩性。
Proc Natl Acad Sci U S A. 2014 Feb 11;111(6):2361-6. doi: 10.1073/pnas.1317527111. Epub 2014 Jan 24.
6
BK potassium channel modulation by leucine-rich repeat-containing proteins.富含亮氨酸重复蛋白对 BK 钾通道的调节。
Proc Natl Acad Sci U S A. 2012 May 15;109(20):7917-22. doi: 10.1073/pnas.1205435109. Epub 2012 Apr 30.

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