Sachs George, Shin Jai Moo, Vagin Olga, Lambrecht Nils, Yakubov Iskandar, Munson Keith
Department of Physiology, David Geffen School of Medicine, University of California at Los Angeles, CA, USA.
J Clin Gastroenterol. 2007 Jul;41 Suppl 2(Suppl 2):S226-42. doi: 10.1097/MCG.0b013e31803233b7.
The recent progress in therapy if acid disease has relied heavily on the performance of drugs targeted against the H,K ATPase of the stomach and the H2 receptor antagonists. It has become apparent in the last decade that the proton pump is the target that has the likelihood of being the most sustainable area of therapeutic application in the regulation of acid suppression. The process of activation of acid secretion requires a change in location of the ATPase from cytoplasmic tubules into the microvilli of the secretory canaliculus of the parietal cell. Stimulation of the resting parietal cell, with involvement of F-actin and ezrin does not use significant numbers of SNARE proteins, because their message is depleted in the pure parietal cell transcriptome. The cell morphology and gene expression suggest a tubule fusion-eversion event. As the active H,K ATPase requires efflux of KCl for activity we have, using the transcriptome derived from 99% pure parietal cells and immunocytochemistry, provided evidence that the KCl pathway is mediated by a KCQ1/KCNE2 complex for supplying K and CLIC6 for supplying the accompanying Cl. The pump has been modeled on the basis of the structures of different conformations of the sr Ca ATPase related to the catalytic cycle. These models use the effects of site directed mutations and identification of the binding domain of the K competitive acid pump antagonists or the defined site of binding for the covalent class of proton pump inhibitors. The pump undergoes conformational changes associated with phosphorylation to allow the ion binding site to change exposure from cytoplasmic to luminal exposure. We have been able to postulate that the very low gastric pH is achieved by lysine 791 motion extruding the hydronium ion bound to carboxylates in the middle of the membrane domain. These models also allow description of the K entry to form the K liganded form of the enzyme and the reformation of the ion site inward conformation thus relating the catalytic cycle of the pump to conformational models. The mechanism of action of the proton pump inhibitor class of drug is discussed along with the cysteines covalently bound with these inhibitors. The review concludes with a discussion of the mechanism of action and binding regions of a possible new class of drug for acid control, the K competitive acid pump antagonists.
酸相关疾病治疗的最新进展在很大程度上依赖于针对胃H⁺,K⁺ -ATP酶的药物以及H₂受体拮抗剂的性能。在过去十年中,质子泵已成为在胃酸抑制调节中最具可持续治疗应用潜力的靶点。胃酸分泌的激活过程需要ATP酶从细胞质小管转移至壁细胞分泌小管的微绒毛中。静息壁细胞的刺激,涉及F -肌动蛋白和埃兹蛋白,并不大量使用SNARE蛋白,因为它们的信息在纯壁细胞转录组中已耗尽。细胞形态和基因表达提示了小管融合 - 外翻事件。由于活性H⁺,K⁺ -ATP酶需要KCl外流来发挥活性,我们利用来自99%纯壁细胞的转录组和免疫细胞化学方法,证明KCl途径由用于供应K⁺的KCQ1/KCNE2复合物和用于供应伴随Cl⁻的CLIC6介导。该泵已基于与催化循环相关的肌浆网Ca²⁺ -ATP酶不同构象的结构进行建模。这些模型利用定点突变的效应以及K⁺竞争性酸泵拮抗剂结合域的鉴定或质子泵抑制剂共价类别的确定结合位点。该泵经历与磷酸化相关的构象变化,以使离子结合位点的暴露从细胞质侧转变为腔侧。我们已经能够推测,极低的胃内pH值是通过赖氨酸791的移动挤出结合在膜结构域中部羧酸盐上的水合氢离子来实现的。这些模型还允许描述K⁺进入以形成酶的K⁺配位形式以及离子位点向内构象的重新形成,从而将泵的催化循环与构象模型联系起来。本文还讨论了质子泵抑制剂类药物的作用机制以及与这些抑制剂共价结合的半胱氨酸。综述最后讨论了一种可能用于胃酸控制的新型药物——K⁺竞争性酸泵拮抗剂的作用机制和结合区域。