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-2,6-sialyltransferase during
normal and cortisone-induced maturation in mouse intestine
1 Shanghai Institute for Pediatric Research, Xinhua Hospital and Shanghai Second Medical University, Shanghai, People's Republic of China 200092; 2 Developmental Gastroenterology Laboratory, Combined Program in Pediatric Gastroenterology and Nutrition, Massachusetts General Hospital and Harvard Medical School, Charlestown 02129; and 3 Program in Glycobiology, Shriver Center for Mental Retardation, Waltham, Massachusetts 02452
Regional differences in the
ontogeny of mouse intestinal
-2,6-sialyltransferase activities
(
-2,6-ST) and the influence of cortisone acetate (CA) on this
expression were determined. High ST activity and
-2,6-ST
mRNA levels were detected in immature small and large intestine, with
activity increasing distally from the duodenum. As the mice matured, ST
activity (predominantly
-2,6-ST) in the small intestine decreased
rapidly to adult levels by the fourth postnatal week. CA precociously
accelerated this region-specific ontogenic decline. A similar decline
of ST mRNA levels reflected ST activity in the small, but not the
large, intestine. Small intestinal sialyl
-2,6-linked
glycoconjugates displayed similar developmental and CA
induced-precocious declines when probed using Sambucus nigra
agglutinin (SNA) lectin. SNA labeling demonstrated age-dependent
diminished sialyl
2,6 glycoconjugate expression in goblet cells in
the small (but not large) intestine, but no such regional specificity
was apparent in microvillus membrane. This suggests differential
regulation of sialyl
-2,6 glycoconjugates in absorptive vs. globlet
cells. These age-dependent and region-specific differences in sialyl
-2,6 glycoconjugates may be mediated in part by altered
-2,6-ST
gene expression regulated by trophic factors such as glucocorticoids.
sialyl
-2,6 glycoconjugates; hormonal regulation; ontogeny of
the gut; lectin
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