Boron Walter F
Department of Cellular and Molecular Physiology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520-8026, USA.
J Am Soc Nephrol. 2006 Sep;17(9):2368-82. doi: 10.1681/ASN.2006060620. Epub 2006 Aug 16.
One of the major tasks of the renal proximal tubule is to secrete acid into the tubule lumen, thereby reabsorbing approximately 80% of the filtered HCO3- as well as generating new HCO3- for regulating blood pH. This review summarizes the cellular and molecular events that underlie four major processes in HCO3- reabsorption. The first is CO2 entry across the apical membrane, which in large part occurs via a gas channel (aquaporin 1) and acidifies the cell. The second process is apical H+ secretion via Na-H exchange and H+ pumping, processes that can be studied using the NH4+ prepulse technique. The third process is the basolateral exit of HCO3- via the electrogenic Na/HCO3 co-transporter, which is the subject of at least 10 mutations that cause severe proximal renal tubule acidosis in humans. The final process is the regulation of overall HCO3- reabsorption by CO2 and HCO3- sensors at the basolateral membrane. Together, these processes ensure that the proximal tubule responds appropriately to acute acid-base disturbances and thereby contributes to the regulation of blood pH.
肾近端小管的主要任务之一是向小管管腔分泌酸,从而重吸收约80%的滤过HCO3-,并生成新的HCO3-以调节血液pH值。本综述总结了HCO3-重吸收过程中四个主要过程的细胞和分子事件。第一个是CO2通过顶膜进入,这在很大程度上是通过气体通道(水通道蛋白1)发生的,并使细胞酸化。第二个过程是通过Na-H交换和H+泵出进行顶膜H+分泌,这些过程可以使用NH4+预脉冲技术进行研究。第三个过程是HCO3-通过电中性Na/HCO3共转运体从基底外侧排出,这是至少10种导致人类严重近端肾小管酸中毒的突变的研究对象。最后一个过程是基底外侧膜上的CO2和HCO3-传感器对整体HCO3-重吸收的调节。这些过程共同确保近端小管对急性酸碱紊乱做出适当反应,从而有助于调节血液pH值。