Division of Nephrology, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
Curr Opin Nephrol Hypertens. 2013 Sep;22(5):572-83. doi: 10.1097/MNH.0b013e328363ff43.
There has been significant progress in our understanding of the structural and functional properties and regulation of the electrogenic sodium bicarbonate cotansporter NBCe1, a membrane transporter that plays a key role in renal acid-base physiology. The NBCe1 variant NBCe1-A mediates basolateral electrogenic sodium-base transport in the proximal tubule and is critically required for transepithelial bicarbonate absorption. Mutations in NBCe1 cause autosomal recessive proximal renal tubular acidosis (pRTA). The review summarizes recent advances in this area.
A topological model of NBCe1 has been established that provides a foundation for future structure-functional studies of the transporter. Critical residues and regions have been identified in NBCe1 that play key roles in its structure, function (substrate transport, electrogenicity) and regulation. The mechanisms of how NBCe1 mutations cause pRTA have also recently been elucidated.
Given the important role of proximal tubule transepithelial bicarbonate absorption in systemic acid-base balance, a clear understanding of the structure-functional properties of NBCe1 is a prerequisite for elucidating the mechanisms of defective transepithelial bicarbonate transport in pRTA.
人们对电中性碳酸氢根共转运体 NBCe1 的结构和功能特性及其调控的理解取得了重大进展。NBCe1 是一种膜转运蛋白,在肾脏酸碱生理学中起着关键作用。NBCe1 变体 NBCe1-A 介导近端肾小管基底外侧的电中性钠-碱基转运,对于跨上皮碳酸氢盐吸收至关重要。NBCe1 的突变导致常染色体隐性近端肾小管酸中毒(pRTA)。本综述总结了该领域的最新进展。
已经建立了 NBCe1 的拓扑模型,为该转运蛋白的未来结构-功能研究奠定了基础。已经确定了 NBCe1 中的关键残基和区域,这些残基和区域在其结构、功能(底物转运、电中性)和调控中起着关键作用。最近还阐明了 NBCe1 突变导致 pRTA 的机制。
鉴于近端肾小管跨上皮碳酸氢盐吸收在全身酸碱平衡中的重要作用,明确 NBCe1 的结构-功能特性是阐明 pRTA 中跨上皮碳酸氢盐转运缺陷的机制的前提。