Differential expression of electrogenic NBC1 (SLC4A4) variants in rat kidney and pancreas.

Biochem Biophys Res Commun

Department of Neuroanatomy, Center for Anatomy, Georg-August-University Göttingen, D-37075 Göttingen, Germany.

Published: February 2004

AI Article Synopsis

  • The study aimed to investigate the expression and localization of two variants of the electrogenic Na(+)-HCO(3)(-) co-transporter NBC1 in rat kidney and pancreas.
  • Two specific antibodies were produced to identify these variants, kNBC1 (in the kidney) and pNBC1 (in the pancreas), with kNBC1 being more prominent in the kidney and pNBC1 in the pancreas.
  • Immunohistochemistry showed that while kNBC1 localized primarily in the kidney's proximal tubules, pNBC1 was present in both pancreas acinar and duct cells, suggesting both variants play a role in bicarbonate transport and pH regulation in these organs.

Article Abstract

The purpose of this study was to determine expression and localization of NH(2)-terminal variants of the electrogenic Na(+)-HCO(3)(-) co-transporter NBC1 (SLC4A4) in the rat kidney and pancreas. We generated two anti-peptide antibodies: alpha333 against the "mste" start (kidney; kNBC1) and alpha332 against the "mede" start (pancreas; pNBC1). Transcripts for both NBC1 variants were detected in kidney and pancreas by RT-PCR, though kNBC1 was more prominent in the kidney and pNBC1 was more prominent in the pancreas. Similar protein expression levels were detected by immunoblotting of plasma membranes (PM) from kidney cortex and pancreas. Immunohistochemistry with alpha333 recognized the "mste"-epitope in the basolateral plasma membrane (BLM) of renal proximal tubule. The "mede"-protein (alpha332) was similarly localized although staining was much less and more diffuse. In the pancreas, alpha332 stained BLM of acinar and duct cells. Some isolated duct cells were also stained at the apical PM. The "mste"-protein (alpha333) was absent in acinar cells but was located at the apical PM of duct cells. The data indicate that the two NH(2)-terminal NBC1 variants are co-expressed in kidney and pancreas, where they may contribute to HCO(3)(-) transport and pH regulation.

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http://dx.doi.org/10.1016/j.bbrc.2003.12.099DOI Listing

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