Laghmani K, Borensztein P, Ambühl P, Froissart M, Bichara M, Moe O W, Alpern R J, Paillard M
Institut National de la Santé et de la Recherche Médicale U.356, Université Pierre et Marie Curie, Centre Hospitalo-Universitaire Broussais, Paris, France.
J Clin Invest. 1997 Jan 1;99(1):24-30. doi: 10.1172/JCI119128.
Chronic metabolic acidosis (CMA) is associated with an adaptive increase in the bicarbonate absorptive capacity of the rat medullary thick ascending limb (MTAL). To specify whether NHE-3, the apical MTAL Na/H exchanger, is involved in this adaptation, NHE-3 mRNA was quantified by a competitive RT-PCR using an internal standard which differed from the wild-type NHE-3 mRNA by an 80-bp deletion. CMA increased NHE-3 mRNA from 0.025+/-0.003 to 0.042+/-0.009 amol/ng total RNA (P < 0.005). NHE-3 transport activity was measured as the initial proton flux rate calculated from the Na-dependent cell pH recovery of Na-depleted acidified MTAL cells in the presence of 50 microM HOE694 which specifically blocks NHE-1, the basolateral MTAL NHE isoform. CMA caused a 68% increase in NHE-3 transport activity (P < 0.001). In addition, CMA was associated with a 71% increase in NHE-3 protein abundance (P < 0.05) as determined by Western blot analysis on MTAL membranes using a polyclonal antiserum directed against a cytoplasmic epitope of rat NHE-3. Thus, NHE-3 adapts to CMA in the rat MTAL via an increase in the mRNA transcript that enhances NHE-3 protein abundance and transport activity.
慢性代谢性酸中毒(CMA)与大鼠髓袢升支粗段(MTAL)重碳酸盐吸收能力的适应性增加有关。为明确顶端MTAL钠/氢交换体NHE-3是否参与这种适应性变化,采用竞争性逆转录聚合酶链反应(RT-PCR)对NHE-3信使核糖核酸(mRNA)进行定量分析,所用内标与野生型NHE-3 mRNA相比有80个碱基对的缺失。CMA使NHE-3 mRNA从0.025±0.003增加至0.042±0.009 amol/ng总RNA(P<0.005)。NHE-3转运活性通过在存在特异性阻断基底外侧MTAL钠/氢交换异构体NHE-1的50μM HOE694时,根据钠缺失酸化MTAL细胞的钠依赖性细胞内pH恢复情况计算出的初始质子通量率来测定。CMA使NHE-3转运活性增加68%(P<0.001)。此外,通过使用针对大鼠NHE-3胞质表位的多克隆抗血清对MTAL膜进行蛋白质印迹分析确定,CMA与NHE-3蛋白丰度增加71%相关(P<0.05)。因此,在大鼠MTAL中,NHE-3通过增加mRNA转录本适应CMA,从而提高NHE-3蛋白丰度和转运活性。