Department of Medicine, University of Toronto and University Health Network, Toronto, Ontario M5S 1A8, Canada.
J Biol Chem. 2011 Feb 18;286(7):5876-83. doi: 10.1074/jbc.M109.089607. Epub 2010 Dec 20.
ATP-sensitive potassium (K(ATP)) channels are regulated by a variety of cytosolic factors (adenine nucleotides, Mg(2+), phospholipids, and pH). We previously reported that K(ATP) channels are also regulated by endogenous membrane-bound SNARE protein syntaxin-1A (Syn-1A), which binds both nucleotide-binding folds of sulfonylurea receptor (SUR)1 and 2A, causing inhibition of K(ATP) channel activity in pancreatic islet β-cells and cardiac myocytes, respectively. In this study, we show that ATP dose-dependently inhibits Syn-1A binding to SUR1 at physiological concentrations, with the addition of Mg(2+) causing a decrease in the ATP-induced inhibitory effect. This ATP disruption of Syn-1A binding to SUR1 was confirmed by FRET analysis in living HEK293 cells. Electrophysiological studies in pancreatic β-cells demonstrated that reduced ATP concentrations increased K(ATP) channel sensitivity to Syn-1A inhibition. Depletion of endogenous Syn-1A in insulinoma cells by botulinum neurotoxin C1 proteolysis followed by rescue with exogenous Syn-1A showed that Syn-1A modulates K(ATP) channel sensitivity to ATP. Thus, our data indicate that although both ATP and Syn-1A independently inhibit β-cell K(ATP) channel gating, they could also influence the sensitivity of K(ATP) channels to each other. These findings provide new insight into an alternate mechanism by which ATP regulates pancreatic β-cell K(ATP) channel activity, not only by its direct actions on Kir6.2 pore subunit, but also via ATP modulation of Syn-1A binding to SUR1.
三磷酸腺苷(ATP)敏感性钾(K(ATP))通道受多种胞质因子(腺嘌呤核苷酸、Mg(2+)、磷脂和 pH 值)调节。我们之前的研究报告表明,K(ATP)通道还受内源性膜结合 SNARE 蛋白突触融合蛋白-1A(Syn-1A)的调节,该蛋白与磺酰脲受体(SUR)1 和 2A 的核苷酸结合折叠都结合,分别导致胰腺β细胞和心肌细胞中 K(ATP)通道活性的抑制。在这项研究中,我们表明 ATP 以生理浓度依赖性方式抑制 Syn-1A 与 SUR1 的结合,加入 Mg(2+)会降低 ATP 诱导的抑制作用。这一 ATP 对 Syn-1A 与 SUR1 结合的破坏通过活 HEK293 细胞中的 FRET 分析得到证实。在胰腺β细胞中的电生理学研究表明,降低的 ATP 浓度增加了 K(ATP)通道对 Syn-1A 抑制的敏感性。用肉毒杆菌神经毒素 C1 蛋白水解作用耗尽胰岛素瘤细胞中的内源性 Syn-1A,然后用外源性 Syn-1A 进行挽救,结果表明 Syn-1A 调节 K(ATP)通道对 ATP 的敏感性。因此,我们的数据表明,尽管 ATP 和 Syn-1A 都独立地抑制β细胞 K(ATP)通道的门控,但它们也可能影响 K(ATP)通道对彼此的敏感性。这些发现为 ATP 调节胰腺β细胞 K(ATP)通道活性的另一种机制提供了新的见解,不仅通过其对 Kir6.2 孔亚基的直接作用,还通过 ATP 对 Syn-1A 与 SUR1 结合的调节。