Abstract

In turtle urinary bladder H<sup>+</sup>- and HCO<sup>-</sup><sub>3</sub> secreting cells, thought to be equipped with either a serosal SITS-sensitive or a luminal anion exchanger, were identified by their Br<sup>-</sup> uptake using electron microprobe analysis. Under all experimental conditions carbonic-anhydrase-rich (CA) cells exhibited a large variation in Cl<sup>–</sup> or anion (sum of Cl<sup>–</sup> and Br<sup>-</sup>) concentrations, ranging between 2 and 55 mmol/kg wet weight (w.w.). From their location within the epithelium and their Br<sup>–</sup> uptake characteristics, CA cells could be divided into three subpopulations: (1) Surface CA cells with a high anion concentration (Σ[C1<sup>-</sup> + Br<sup>-</sup>] ≧ 20 mmol/kg w.w.) were regarded as H<sup>+</sup>-secreting cells since the high serosal Br<sup>–</sup> uptake within 7 min was similar to that expected from current models of H<sup>+</sup> secretion, and could be reduced by serosal SITS or a luminal pH of 4.5. (2) Surface CA cells with a low anion concentration and low serosal, but substantial luminal, Br<sup>–</sup> uptake were considered to be HCO<sup>-</sup><sub>3</sub>-secreting cells. (3) CA cells without visible contact with the luminal surface and an intermediate Br<sup>–</sup> uptake seem to represent surface CA cell precursors. The SITS inhibitable serosal Br<sup>–</sup> uptake into granular and basal cells indicates the presence of a serosal anion exchanger, possibly involved in acid-base regulation of these cells.

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