expedited article Expression and distribution of the Na 1 -HCO 3 cotransporter in human pancreas

Expression and distribution of the Na 1 -HCO 3 2 cotransporter in human pancreas. Am. J. Physiol. 277 ( Gastrointest. Liver Physiol. 40): G487– G494, 1999.—The cellular mechanisms of HCO 3 2 secretion in the human pancreas are unclear. Expression of a Na 1 -HCO 3 2 cotransporter (NBC) mRNA has been observed recently, but the distribution and physiological role of the NBC protein are not known. Here we examined the expression and localization of NBC in human pancreas by Northern blot, immunoblot, and immunofluorescence microscopy. Rat kidney NBC probes detected a single 9.5-kb band by Northern blot. On immunoblots, two polyclonal antisera directed against different epitopes of rat kidney NBC identified a single , 130-kDa protein. In cryosections of normal human pancreas, both antisera labeled basolateral membranes of large, morphologically identifiable ducts and produced a distinct labeling pattern in the remainder of the parenchyma. In double-labeling experiments, NBC immunoreactivity in the parenchyma colocalized with the Na 1 -K 1 pump, a basolateral marker. In contrast, NBC and cystic fibrosis transmembrane conductance regulator, an apical membrane marker, were detected within the same histological structures but at different subcellular local-izations. The NBC antisera did not label acinar or islet cells. Our observations suggest that secretion of HCO 3 2 by human pancreatic duct cells involves the basolateral uptake of Na 1 and HCO 3 2 via NBC, an electrogenic Na 1 -HCO 3 2 cotransporter.