Retinol enhances differentiation of the gastric parietal cell lineage in developing rabbits

Cell Physiol Biochem. 2004;14(4-6):333-42. doi: 10.1159/000080343.

Abstract

In the gastric glands, parietal cells are the targets for anti-ulcer drugs because they contain the proton pump or HK-ATPase responsible for acid secretion. Little is known about factors influencing developmental expression and activity of HK-ATPase. In this study, the parietal cell lineage was investigated in rabbits at post-natal days 0 (P0) to P60 by using morphological and biochemical methods. Immunohistochemical and ultrastructural studies show that the HK-ATPase-expressing cells that appear at P0 and P3 are pre-parietal cells. However, terminally differentiated, mature parietal cells make their appearance at P7. These data correlate with the activity of HK-ATPase, measured as K(+)-dependent hydrolysis of p-nitrophenyl phosphate. Three-day-retinol treatment of P3-P30 rabbits induced an increase in the (i) production of parietal cells, (ii) intensity of the HK-ATPase immunostaining per cell, (iii) activity of HK-ATPase and (iv) amount of HK-ATPase protein measured by Western blotting. In conclusion, retinol upregulates the development of HK-ATPase in rabbits, perhaps due to precocious acceleration of the differentiation program of parietal cell lineage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Ulcer Agents / pharmacology
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cell Lineage / drug effects
  • Cell Lineage / physiology
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / growth & development*
  • Gastric Mucosa / immunology
  • H(+)-K(+)-Exchanging ATPase / analysis
  • H(+)-K(+)-Exchanging ATPase / metabolism*
  • Parietal Cells, Gastric / cytology*
  • Parietal Cells, Gastric / drug effects
  • Parietal Cells, Gastric / ultrastructure
  • Rabbits
  • Vitamin A / pharmacology*

Substances

  • Anti-Ulcer Agents
  • Vitamin A
  • H(+)-K(+)-Exchanging ATPase