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Acidic pH of the lateral intercellular spaces of MDCK cells cultured on permeable supports
Authors:J. -Y. Chatton  K. R. Spring
Affiliation:(1) Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Building 10, Room 6N307, 20892 Bethesda, Maryland
Abstract:The pH of the lateral intercellular space (LIS) of Madin-Darby canine kidney (MDCK) cell monolayers grown on permeable supports was investigated by microspectrofluorimetry using BCECF (2prime,7prime-bis(carboxyethyl)-5,6-carboxyfluorescein). The permeability of the support was selectively reduced by growing ZnAl-silicate crystals inside its pores. The diffusion of BCECF across the filter was sufficiently retarded to allow measurements of fluorescence in the LIS. The LIS pH and intracellular pH of the cells surrounding them were determined in HEPES-buffered solutions. When the perfusate pH was 7.4, the LIS pH was more acidic (7.06±0.02) and equaled the cytoplasmic pH (7.08±0.05). When perfusate was changed to pH 7.0 or 7.8, the LIS changed linearly by about half the magnitude of the perfusate pH. Intracellular pH followed LIS pH variations between perfusate pH 7.0 and 7.4 but was significantly higher when perfusate pH was 7.8. Tight junctional H+ permeability was undetectably low. The low steady-state pH in the LIS was not altered by inhibitors of acid transport or low temperature. Rapid perturbations of pH in the LIS showed that protons were not immobilized in the LIS. The acidic microenvironment within the LIS may be the result of buffering by the cell surface proteins.We are indebted to Dr. M.V. King (Wadsworth Center for Laboratories and Research, Albany, NY) for introducing us to the chemistry of silicates. J.-Y.C. is supported in part by the Ciba-Geigy Jubiläums Stiftung (Basel, Switzerland) and the Fondation Académique Vaudoise (Lausanne, Switzerland).
Keywords:Epithelia  Fluid transport  Fluorescence microscopy  Tissue culture
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