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过氧化氢通过蛋白激酶 C 刺激动脉平滑肌 L 型钙通道。

Stimulation of arterial smooth muscle L-type calcium channels by hydrogen peroxide requires protein kinase C.

机构信息

Vascular Physiology Research Group, Department of Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.

出版信息

Channels (Austin). 2012 Sep-Oct;6(5):385-9. doi: 10.4161/chan.21708. Epub 2012 Aug 21.

Abstract

Changes in intracellular calcium regulate countless biological processes. In arterial smooth muscle, voltage-dependent L-type calcium channels are major conduits for calcium entry with the primary function being determination of arterial diameter. Similarly, changes in intracellular redox status, either discrete controlled changes or global pathological perturbations, are also critical determinants of cell function. We recently reported that in arterial smooth muscle cells, local generation of hydrogen peroxide leads to colocalized calcium entry through L-type calcium channels. Here we extend our investigation into mechanisms linking hydrogen peroxide to calcium influx through L-type calcium channels by focusing on the role of protein kinase C (PKC). Our data indicate that stimulation of L-type calcium channels by hydrogen peroxide requires oxidant-dependent increases in PKC catalytic activity. This effect is independent of classical cofactor-dependent activation of PKC by diacylglycerol. These data provide additional experimental evidence supporting the concept of oxidative stimulation of L-type calcium channels.

摘要

细胞内钙离子的变化调节着无数的生物过程。在动脉平滑肌中,电压依赖性 L 型钙通道是钙离子内流的主要途径,其主要功能是决定动脉直径。同样,细胞内氧化还原状态的变化,无论是离散的控制变化还是全局的病理扰动,也是细胞功能的关键决定因素。我们最近报道,在动脉平滑肌细胞中,局部产生的过氧化氢导致通过 L 型钙通道的局部钙内流。在这里,我们通过关注蛋白激酶 C(PKC)的作用,将我们的研究扩展到将过氧化氢与通过 L 型钙通道的钙内流联系起来的机制。我们的数据表明,过氧化氢刺激 L 型钙通道需要氧化还原依赖的 PKC 催化活性增加。这种作用独立于二酰基甘油经典的辅助因子依赖性 PKC 激活。这些数据提供了额外的实验证据,支持 L 型钙通道的氧化刺激概念。

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