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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS
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
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