Ismailov I I, Benos D J
Department of Physiology and Biophysics, University of Alabama at Birmingham, USA.
Kidney Int. 1995 Oct;48(4):1167-79. doi: 10.1038/ki.1995.400.
A fundamental property of ion channels is their ability to be modulated by intracellular second messenger systems acting via covalent modifications of the channel protein itself. One such important biochemical reaction is phosphorylation on serine, threonine, and tyrosine residues. Ion channels in the kidney are no exception. Moreover, many ion channels, including many amiloride-sensitive epithelial Na+ channels, are subject to modulation by a multiplicity of inputs. For example, renal Na+ channels are not gated by voltage in their unphosphorylated state. However, upon phosphorylation by PKA plus ATP, these channels become voltage-dependent as well as having their open probability increased. Phosphorylation by PKC inhibits channel activity regardless of whether the channel was previously phosphorylated by PKA. Likewise, Na+ channel ADP-ribosylation by PTX overrides the actions of cAMP-dependent phosphorylation. Consistent with this idea is the fact that the phosphorylation sites for PKA and PKC and the ADP-ribosylation sites occur on different polypeptides comprising the channel complex. Epithelial Na+ channel activity is also regulated by methylation, arachidonic acid metabolites, and by interactions with cytoskeletal components. An exciting new age in understanding renal Na+ channel function has begun. Canessa and collaborators [103, 104] and Lingueglia et al [105] have, for the first time, identified by expression cloning an amiloride-sensitive Na+ channel from rat distal colon. The messenger RNA encoding the subunits comprising this channel are expressed in the distal tubule and cortical collecting tubule of the kidney (Rossier, unpublished observations). In addition, our laboratory has successfully cloned a mammalian homologue of this same channel from bovine renal papillary collecting ducts [106].(ABSTRACT TRUNCATED AT 250 WORDS)
离子通道的一个基本特性是它们能够被细胞内第二信使系统所调节,这些系统通过对通道蛋白本身进行共价修饰来发挥作用。一种这样重要的生化反应是丝氨酸、苏氨酸和酪氨酸残基的磷酸化。肾脏中的离子通道也不例外。此外,许多离子通道,包括许多对阿米洛利敏感的上皮钠通道,会受到多种输入信号的调节。例如,肾钠通道在未磷酸化状态下不受电压门控。然而,在被蛋白激酶A(PKA)加ATP磷酸化后,这些通道变得依赖电压,并且开放概率增加。蛋白激酶C(PKC)的磷酸化会抑制通道活性,无论该通道之前是否被PKA磷酸化。同样,百日咳毒素(PTX)介导的钠通道ADP核糖基化会推翻cAMP依赖性磷酸化的作用。与此观点一致的是,PKA和PKC的磷酸化位点以及ADP核糖基化位点位于构成通道复合体的不同多肽上。上皮钠通道活性还受甲基化、花生四烯酸代谢产物以及与细胞骨架成分相互作用的调节。理解肾钠通道功能的一个激动人心的新时代已经开启。卡内萨及其合作者[103, 104]以及林格利亚等人[105]首次通过表达克隆从大鼠远端结肠中鉴定出一种对阿米洛利敏感的钠通道。编码构成该通道亚基的信使核糖核酸在肾脏的远端小管和皮质集合小管中表达(罗西耶,未发表的观察结果)。此外,我们实验室已成功从牛肾乳头集合管中克隆出该通道的一个哺乳动物同源物[106]。(摘要截选至250词)