Stewart A K, Yamamoto A, Nakakuki M, Kondo T, Alper S L, Ishiguro H
Renal Division, Molecular and Vascular Medicine Unit, Beth Israel Deaconess Med. Ctr., 330 Brookline Ave., Boston, MA 02215, USA.
Am J Physiol Gastrointest Liver Physiol. 2009 Jun;296(6):G1307-17. doi: 10.1152/ajpgi.90697.2008. Epub 2009 Apr 2.
Pancreatic ductal epithelium produces a HCO(3)(-)-rich fluid. HCO(3)(-) transport across ductal apical membranes has been proposed to be mediated by both SLC26-mediated Cl(-)/HCO(3)(-) exchange and CFTR-mediated HCO(3)(-) conductance, with proportional contributions determined in part by axial changes in gene expression and luminal anion composition. In this study we investigated the characteristics of apical Cl(-)/HCO(3)(-) exchange and its functional interaction with Cftr activity in isolated interlobular ducts of guinea pig pancreas. BCECF-loaded epithelial cells of luminally microperfused ducts were alkalinized by acetate prepulse or by luminal Cl(-) removal in the presence of HCO(3)(-)-CO(2). Intracellular pH recovery upon luminal Cl(-) restoration (nominal Cl(-)/HCO(3)(-) exchange) in cAMP-stimulated ducts was largely inhibited by luminal dihydro-DIDS (H(2)DIDS), accelerated by luminal CFTR inhibitor inh-172 (CFTRinh-172), and was insensitive to elevated bath K(+) concentration. Luminal introduction of CFTRinh-172 into sealed duct lumens containing BCECF-dextran in HCO(3)(-)-free, Cl(-)-rich solution enhanced cAMP-stimulated HCO(3)(-) secretion, as calculated from changes in luminal pH and volume. Luminal Cl(-) removal produced, after a transient small depolarization, sustained cell hyperpolarization of approximately 15 mV consistent with electrogenic Cl(-)/HCO(3)(-) exchange. The hyperpolarization was inhibited by H(2)DIDS and potentiated by CFTRinh-172. Interlobular ducts expressed mRNAs encoding CFTR, Slc26a6, and Slc26a3, as detected by RT-PCR. Thus Cl(-)-dependent apical HCO(3)(-) secretion in pancreatic duct is mediated predominantly by an Slc26a6-like Cl(-)/HCO(3)(-) exchanger and is accelerated by inhibition of CFTR. This study demonstrates functional coupling between Cftr and Slc26a6-like Cl(-)/HCO(3)(-) exchange activity in apical membrane of guinea pig pancreatic interlobular duct.
胰腺导管上皮细胞产生富含HCO₃⁻的液体。有人提出,HCO₃⁻跨导管顶端膜的转运是由SLC26介导的Cl⁻/HCO₃⁻交换和CFTR介导的HCO₃⁻电导共同介导的,其比例贡献部分由基因表达的轴向变化和管腔阴离子组成决定。在本研究中,我们研究了豚鼠胰腺小叶间导管中顶端Cl⁻/HCO₃⁻交换的特征及其与Cftr活性的功能相互作用。在HCO₃⁻-CO₂存在的情况下,通过醋酸盐预脉冲或管腔Cl⁻去除,使经微灌注管腔的BCECF负载的上皮细胞碱化。在cAMP刺激的导管中,管腔Cl⁻恢复时(名义上的Cl⁻/HCO₃⁻交换)细胞内pH的恢复在很大程度上受到管腔二氢-DIDS(H₂DIDS)的抑制,受到管腔CFTR抑制剂inh-172(CFTRinh-172)的加速,并且对升高的浴液K⁺浓度不敏感。将CFTRinh-172管腔引入含有BCECF-葡聚糖的密封导管管腔中,在无HCO₃⁻、富含Cl⁻的溶液中,根据管腔pH和体积的变化计算,增强了cAMP刺激的HCO₃⁻分泌。管腔Cl⁻去除在短暂的小去极化后,产生了约15 mV的持续细胞超极化,这与电中性Cl⁻/HCO₃⁻交换一致。超极化受到H₂DIDS的抑制,并被CFTRinh-172增强。通过RT-PCR检测,小叶间导管表达编码CFTR、Slc26a6和Slc26a3的mRNA。因此,胰腺导管中依赖Cl⁻的顶端HCO₃⁻分泌主要由一种类似Slc26a6的Cl⁻/HCO₃⁻交换体介导,并通过抑制CFTR而加速。本研究证明了豚鼠胰腺小叶间导管顶端膜中Cftr与类似Slc26a6的Cl⁻/HCO₃⁻交换活性之间的功能偶联。