Fejes-Tóth G, Chen W R, Rusvai E, Moser T, Náray-Fejes-Tóth A
Department of Physiology, Dartmouth Medical School, Lebanon, New Hampshire 03756.
J Biol Chem. 1994 Oct 28;269(43):26717-21.
The cortical collecting duct of the kidney contains two types of intercalated cells that transport HCO3 in opposite directions. HCO3 reabsorption takes place in the alpha-type intercalated cells, which express a Cl/HCO3 exchanger on the basolateral membrane. This exchanger is the product of the anion exchanger 1 (AE1) or band 3 gene. HCO3 secretion occurs in the beta-intercalated cells, which have a Cl/HCO3 exchanger on the apical membrane. Based on studies in an immortalized cell line, recently it was proposed that the apical anion exchanger of beta-intercalated cells is also AE1 (van Adelsberg, J. S., Edwards, J. C., and Al-Awqati, Q. (1993) J. Biol. Chem. 268, 11283-11289). In the present study we reinvestigated this issue by determining the distribution of AE1 mRNA and protein in the two intercalated cell types using cells freshly isolated from the native epithelium. Using quantitative reverse transcriptase polymerase chain reaction, we found that alpha-intercalated cells, isolated from rabbit kidney by fluorescence-activated cell sorting, have high levels of AE1 mRNA, whereas beta-intercalated cells express very low levels. The ratio of AE1 mRNA levels in alpha- versus beta-intercalated cells averaged 10.1 +/- 2.6. In addition, metabolic acidosis increased the levels of AE1 mRNA by 3-5-fold in cortical collecting duct cells. This difference was confirmed by Northern blotting. Western blotting using an antibody against rabbit AE1 revealed a major immunoreactive product with a molecular weight of approximately 110 kDa in cortical collecting duct cells. Deglycosylation reduced the size of the immunoreactive product to approximately 90 kDa, which is compatible with the presence of a truncated form of AE1. Metabolic acidosis increased the intensity of the AE1 immunoreactive band. The level of AE1-immunoreactive protein was significantly higher in alpha-intercalated cells than in beta-intercalated cells. In aggregate, these data provide evidence for the differential expression of AE1 in HCO3-reabsorbing versus HCO3-secreting renal intercalated cells both at the mRNA and at the protein level. These results give no support to the concept that AE1 functions both as a basolateral and an apical anion exchanger in cortical collecting duct cells.
肾皮质集合管包含两种类型的闰细胞,它们以相反方向转运HCO3。HCO3重吸收发生在α型闰细胞中,这些细胞在基底外侧膜上表达一种Cl/HCO3交换体。这种交换体是阴离子交换体1(AE1)或带3基因的产物。HCO3分泌发生在β闰细胞中,这些细胞在顶端膜上有一个Cl/HCO3交换体。基于对一种永生化细胞系的研究,最近有人提出β闰细胞的顶端阴离子交换体也是AE1(van Adelsberg, J. S., Edwards, J. C., and Al-Awqati, Q. (1993) J. Biol. Chem. 268, 11283 - 11289)。在本研究中,我们通过使用从天然上皮组织新鲜分离的细胞来确定AE1 mRNA和蛋白在两种闰细胞类型中的分布,从而重新研究了这个问题。使用定量逆转录聚合酶链反应,我们发现通过荧光激活细胞分选从兔肾中分离出的α闰细胞具有高水平的AE1 mRNA,而β闰细胞表达的水平非常低。α闰细胞与β闰细胞中AE1 mRNA水平的平均比值为10.1±2.6。此外,代谢性酸中毒使皮质集合管细胞中AE1 mRNA水平增加了3至5倍。Northern印迹法证实了这种差异。使用抗兔AE1抗体的Western印迹法显示,在皮质集合管细胞中有一个主要的免疫反应产物,其分子量约为110 kDa。去糖基化使免疫反应产物的大小减小到约90 kDa,这与截短形式的AE1的存在相符。代谢性酸中毒增加了AE1免疫反应条带的强度。α闰细胞中AE1免疫反应蛋白的水平明显高于β闰细胞。总的来说,这些数据为AE1在重吸收HCO3与分泌HCO3的肾闰细胞中的差异表达提供了mRNA和蛋白水平的证据。这些结果不支持AE1在皮质集合管细胞中既作为基底外侧阴离子交换体又作为顶端阴离子交换体发挥作用的概念。