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Am J Physiol Cell Physiol 285: C737-C749, 2003. First published May 28, 2003; doi:10.1152/ajpcell.00041.2003
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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

More than apical: distribution of SGLT1 in Caco-2 cells

Helmut Kipp, Saeed Khoursandi, Daniel Scharlau, and Rolf K. H. Kinne

Abteilung Epithelphysiologie, Max-Planck-Institut für molekulare Physiologie, 44227 Dortmund, Germany

Submitted 28 January 2003 ; accepted in final form 27 May 2003

We investigated the distribution of the endogenous sodium-D-glucose cotransporter (SGLT1) in polarized Caco-2 cells, a model for enterocytes. A cellular organelle fraction was separated by free-flow electrophoresis and subjected to the analysis of endogenous and exogenous marker enzymes for various membrane vesicle components. Furthermore, the presence of SGLT1 was tested by an ELISA assay employing newly developed epitope specific antibodies. Thereby it was found that the major amount of SGLT1 resided in intracellular compartments and only a minor amount in apical plasma membranes. The distribution ratio between intracellular SGLT1 and apical membrane-associated SGLT1 was ~2:1. Further immunocytochemical investigation of SGLT1 distribution in fixed Caco-2 cells by epifluorescence and confocal microscopy revealed that the intracellular compartments containing SGLT1 were associated with microtubules. Elimination of SGLT1 synthesis by incubation of cells with cycloheximide did not significantly reduce the size of the intracellular SGLT1 pool. Furthermore, the half-life of SGLT1 in Caco-2 cells was determined to be 2.5 days by metabolic labeling followed by immunoprecipitation. Our data suggest that most of the intracellular SGLT1 are not transporters en route from biosynthesis to their cellular destination but represent an intracellular reserve pool. We therefore propose that intracellular compartments containing SGLT1 are involved in the regulation of SGLT1 abundance at the apical cell surface.

endosome; microtubules; enterocyte; D-glucose transport; antibodies



Address for reprint requests and other correspondence: H. Kipp, Max-Planck-Institut für molekulare Physiologie, Postfach 50 02 47, 44202 Dortmund, Germany (E-mail: helmut.kipp{at}mpi-dortmund.mpg.de).




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