Glucocorticoid regulation and glycosylation of mouse intestinal type IIb Na-P(i) cotransporter during ontogeny

Am J Physiol Gastrointest Liver Physiol. 2002 Aug;283(2):G426-34. doi: 10.1152/ajpgi.00319.2001.

Abstract

We sought to characterize expression of an apically expressed intestinal Na-P(i) cotransporter (Na-P(i)-IIb) during mouse ontogeny and to assess the effects of methylprednisolone (MP) treatment. In control mice, Na-P(i) uptake by intestinal brush-border membrane vesicles was highest at 14 days of age, lower at 21 days, and further reduced at 8 wk and 8-9 mo of age. Na-P(i)-IIb mRNA and immunoreactive protein levels in 14-day-old animals were markedly higher than in older groups. MP treatment significantly decreased Na-P(i) uptake and Na-P(i)-IIb mRNA and protein expression in 14-day-old mice. Additionally, the size of the protein was smaller in 14-day-old mice. Deglycosylation of protein from 14-day-old and 8-wk-old animals with peptide N-glycosidase reduced the molecular weight to the predicted size. We conclude that intestinal Na-P(i) uptake and Na-P(i)-IIb expression are highest at 14 days and decrease with age. Furthermore, MP treatment reduced intestinal Na-P(i) uptake approximately threefold in 14-day-old mice and this reduction correlates with reduced Na-P(i)-IIb mRNA and protein expression. We also demonstrate that Na-P(i)-IIb is an N-linked glycoprotein and that glycosylation is age dependent.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aging / physiology*
  • Amino Acid Sequence / genetics
  • Animals
  • Animals, Newborn / growth & development
  • Animals, Newborn / physiology*
  • Animals, Suckling / physiology
  • Blotting, Northern
  • Glycoside Hydrolases / pharmacology
  • Glycosylation
  • Immune Sera / immunology
  • Intestinal Mucosa / metabolism*
  • Male
  • Methylprednisolone / pharmacology*
  • Mice
  • Mice, Inbred C57BL
  • Microvilli / metabolism
  • Molecular Sequence Data
  • Protein Isoforms / immunology
  • Protein Isoforms / metabolism
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Phosphate Cotransporter Proteins, Type IIb
  • Symporters / genetics
  • Symporters / immunology
  • Symporters / metabolism*
  • Weaning

Substances

  • Immune Sera
  • Protein Isoforms
  • Slc34a2 protein, mouse
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Phosphate Cotransporter Proteins, Type IIb
  • Symporters
  • Glycoside Hydrolases
  • Methylprednisolone