Doi T, Fakler B, Schultz J H, Schulte U, Brändle U, Weidemann S, Zenner H P, Lang F, Ruppersberg J P
Department of Sensory Biophysics, Ear-Nose-and-Throat Hospital of the University of Tübingen, Germany.
J Biol Chem. 1996 Jul 19;271(29):17261-6. doi: 10.1074/jbc.271.29.17261.
The channels that control K+ homeostasis by mediating K+ secretion across the apical membrane of renal tubular cells have recently been cloned and designated ROMK1, -2, and -3. Native apical K+ channels are indirectly regulated by the K+ concentration at the basolateral membrane through a cascade of intracellular second messengers. It is shown here that ROMK1 (Kir1.1) channels are also directly regulated by the extracellular (apical) K+ concentration, and that this K+ regulation is coupled to intracellular pH. The K+ regulation and its coupling to pH were assigned to different structural parts of the channel protein. K+ regulation is determined by the core region, which comprises the two hydrophobic segments M1 and M2 and the P region. Decoupling from pH was achieved by exchanging the N terminus of ROMK1 by that of the pH-insensitive channel IRK1 (Kir2.1). These results suggest an allosteric regulation of ROMK1 channels by extracellular K+ and intracellular pH, which may represent a novel link between K+ homeostasis and pH control.
最近,通过介导肾小管细胞顶端膜钾离子分泌来控制钾离子稳态的通道已被克隆,并命名为ROMK1、ROMK2和ROMK3。天然顶端钾离子通道通过一系列细胞内第二信使间接受基底外侧膜钾离子浓度调节。本文表明,ROMK1(Kir1.1)通道也直接受细胞外(顶端)钾离子浓度调节,且这种钾离子调节与细胞内pH值相关。钾离子调节及其与pH值的关联被归因于通道蛋白的不同结构部分。钾离子调节由核心区域决定,该区域包括两个疏水片段M1和M2以及P区域。通过用pH不敏感通道IRK1(Kir2.1)的N末端替换ROMK1的N末端,实现了与pH值的解偶联。这些结果表明,细胞外钾离子和细胞内pH值对ROMK1通道存在变构调节,这可能代表了钾离子稳态与pH值控制之间的一种新联系。