The Water Channel Aquaporin-8 Is Mainly Intracellular in Rat Hepatocytes, and Its Plasma Membrane Insertion Is Stimulated by Cyclic AMP

• Published in: The Journal of biological chemistry Vol. 276; no. 15; pp. 12147 - 12152
• Main Authors: Garcı́a, Fabiana, Kierbel, Arlinet, Larocca, M.Cecilia, Gradilone, Sergio A., Splinter, Patrick, LaRusso, Nicholas F., Marinelli, Raúl A.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 13.04.2001; American Society for Biochemistry and Molecular Biology
• Subjects: Animals; Aquaporins - metabolism; Bucladesine - pharmacology; Cell Membrane - metabolism; Cells, Cultured; Colchicine - pharmacology; Hepatocytes - drug effects; Hepatocytes - metabolism; Ion Channels; Male; Rats; Rats, Wistar; Subcellular Fractions - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M009403200

We previously found that water transport across hepatocyte plasma membranes occurs mainly via a non-channel mediated pathway. Recently, it has been reported that mRNA for the water channel, aquaporin-8 (AQP8), is present in hepatocytes. To further explore this issue, we studied protein expression, subcellular localization, and regulation of AQP8 in rat hepatocytes. By subcellular fractionation and immunoblot analysis, we detected anN-glycosylated band of ∼34 kDa corresponding to AQP8 in hepatocyte plasma and intracellular microsomal membranes. Confocal immunofluorescence microscopy for AQP8 in cultured hepatocytes showed a predominant intracellular vesicular localization. Dibutyryl cAMP (Bt2cAMP) stimulated the redistribution of AQP8 to plasma membranes. Bt2cAMP also significantly increased hepatocyte membrane water permeability, an effect that was prevented by the water channel blocker dimethyl sulfoxide. The microtubule blocker colchicine but not its inactive analog lumicolchicine inhibited the Bt2cAMP effect on both AQP8 redistribution to cell surface and hepatocyte membrane water permeability. Our data suggest that in rat hepatocytes AQP8 is localized largely in intracellular vesicles and can be redistributed to plasma membranes via a microtubule-depending, cAMP-stimulated mechanism. These studies also suggest that aquaporins contribute to water transport in cAMP-stimulated hepatocytes, a process that could be relevant to regulated hepatocyte bile secretion.