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Departments of Pathology and Medicine, Northwestern University Medical School, Chicago, Illinois 60611
Expression and role of sodium glucose cotransporter (SGLT-1) in
tubulogenesis were investigated during renal development. A mouse
SGLT-1 cDNA was cloned, and it had substantial homology with human and
rat forms. Four mRNA transcripts were detected, which differed in size
from other species. SGLT-1 transcripts were detected at day
13 of gestation, and their expression increased during later
stages extending into the postnatal period. A high mRNA and protein
expression of SGLT-1 was seen in tubular segments of the inner cortex
and outer medulla at day 16, and it was developmentally regulated. Treatment with SGLT-1 antisense selectively decreased the
population of tubules in the metanephric explants. Expression of
glomerular mRNA and WGA binding were unchanged. SGLT-1 activity, as
measured by [14C]methyl-
-D-glucopyranoside
uptake, increased during gestation in the tubular segments where it is
expressed. Glucose uptake was inhibited by the treatment with SGLT-1
antisense and D-galactose. The data suggest that SGLT-1
exhibits a restricted spatiotemporal expression with functional
activity confined to the corresponding tubular segments, and it
selectively maintains renal tubulogenesis during development.
renal development
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