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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Membrane trafficking of large conductance Ca2+- and voltage-activated K+ (BK) channels is regulated by Rab4 GTPase
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Membrane trafficking of large conductance Ca2+- and voltage-activated K+ (BK) channels is regulated by Rab4 GTPase

机译:通过Rab4 GTP酶调节大电导Ca2 +和电压激活的K +(BK)通道的膜运输

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摘要

The large conductance voltage- and Ca2+ activated K+ (BK) channel is a major ionic determinant of vascular tone, vasodilation, and blood pressure. The activity of BK channels is regulated in part by membrane presentation. Rab GTPase (Rab) regulates important cellular processes, including ion channel membrane trafficking. We hypothesize that Rab4a participates in the regulation of BK channel alpha-subunit (BK-alpha) membrane trafficking. We found that vascular BK-alpha interacts physically with Rab4a. Co-expression of dominant-negative Rab4a reduced BK-alpha surface expression, whereas that of constitutively-active Rab4a augmented BK-alpha surface presentation. These novel findings suggest that vascular BK channel membrane expression is regulated by Rab4a through channel membrane trafficking.
机译:大电导电压和Ca2 +活化的K +(BK)通道是血管间调,血管血管和血压的主要离子决定簇。 BK通道的活性部分地通过膜呈现来调节。 Rab GTPase(RAB)调节重要的细胞过程,包括离子通道膜贩运。 我们假设RAB4A参与BK通道α-亚基(BK-α)膜运输的调节。 我们发现血管BK-alpha与Rab4a合作。 显性阴性Rab4a的共同表达降低了BK-α表面表达,而组成型活性Rab4a增强BK-α表面呈列的表达。 这些新发现表明,血管BK沟道膜表达通过兔子通过沟道膜运输来调节。

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