Féraille E, Doucet A
Division of Nephrology, Geneva University Hospital, Geneva, Switzerland.
Physiol Rev. 2001 Jan;81(1):345-418. doi: 10.1152/physrev.2001.81.1.345.
Tubular reabsorption of filtered sodium is quantitatively the main contribution of kidneys to salt and water homeostasis. The transcellular reabsorption of sodium proceeds by a two-step mechanism: Na(+)-K(+)-ATPase-energized basolateral active extrusion of sodium permits passive apical entry through various sodium transport systems. In the past 15 years, most of the renal sodium transport systems (Na(+)-K(+)-ATPase, channels, cotransporters, and exchangers) have been characterized at a molecular level. Coupled to the methods developed during the 1965-1985 decades to circumvent kidney heterogeneity and analyze sodium transport at the level of single nephron segments, cloning of the transporters allowed us to move our understanding of hormone regulation of sodium transport from a cellular to a molecular level. The main purpose of this review is to analyze how molecular events at the transporter level account for the physiological changes in tubular handling of sodium promoted by hormones. In recent years, it also became obvious that intracellular signaling pathways interacted with each other, leading to synergisms or antagonisms. A second aim of this review is therefore to analyze the integrated network of signaling pathways underlying hormone action. Given the central role of Na(+)-K(+)-ATPase in sodium reabsorption, the first part of this review focuses on its structural and functional properties, with a special mention of the specificity of Na(+)-K(+)-ATPase expressed in renal tubule. In a second part, the general mechanisms of hormone signaling are briefly introduced before a more detailed discussion of the nephron segment-specific expression of hormone receptors and signaling pathways. The three following parts integrate the molecular and physiological aspects of the hormonal regulation of sodium transport processes in three nephron segments: the proximal tubule, the thick ascending limb of Henle's loop, and the collecting duct.
滤过钠的肾小管重吸收在数量上是肾脏对盐和水平衡的主要贡献。钠的跨细胞重吸收通过两步机制进行:钠钾ATP酶驱动的基底外侧主动排钠允许钠通过各种钠转运系统被动地从顶端进入。在过去15年里,大多数肾钠转运系统(钠钾ATP酶、通道、协同转运体和交换体)已在分子水平上得到表征。结合20世纪60年代至80年代开发的用于规避肾脏异质性并在单个肾单位节段水平分析钠转运的方法,转运体的克隆使我们对钠转运激素调节的理解从细胞水平提升到分子水平。本综述的主要目的是分析转运体水平的分子事件如何解释激素促进的肾小管钠处理的生理变化。近年来,细胞内信号通路之间相互作用导致协同或拮抗也变得明显。因此,本综述的第二个目的是分析激素作用背后的信号通路整合网络。鉴于钠钾ATP酶在钠重吸收中的核心作用,本综述的第一部分重点关注其结构和功能特性,特别提及肾小管中表达的钠钾ATP酶的特异性。在第二部分中,在更详细讨论激素受体和信号通路的肾单位节段特异性表达之前,简要介绍激素信号传导的一般机制。接下来的三个部分整合了三个肾单位节段(近端小管、亨氏袢厚升支和集合管)中钠转运过程激素调节的分子和生理方面。