Regulation of lactase and sucrase-isomaltase gene expression in the duodenum during childhood

J Pediatr Gastroenterol Nutr. 1998 Jul;27(1):37-46. doi: 10.1097/00005176-199807000-00007.

Abstract

Background: In children, lactase and sucrase-isomaltase are essential intestinal glycohydrolases, and insufficiency of either enzyme causes diarrhea and malnutrition. Little is known about the regulation of lactase and sucrase-isomaltase expression in the duodenum during childhood. In this study, the mechanisms of regulation of duodenal expression of both enzymes were examined in a study population with ages ranging from 1 to 18 years.

Methods: Duodenal biopsy specimens from 60 white children were used to analyze tissue morphology and to quantify lactase and sucrase-isomaltase mRNA and protein.

Results: Among healthy subjects, high interindividual variability was noted in both mRNA and protein levels for lactase and sucrase-isomaltase. Lactase mRNA level per subject did not correlate with sucrase-isomaltase mRNA level and thus appeared independent. Both lactase and sucrase-isomaltase protein levels correlated significantly with their respective mRNA levels. For each enzyme, a significant inverse correlation was observed between the degree of villus atrophy and mRNA levels. Aging from 1 to 18 years did not result in significant changes in mRNA or protein levels of either enzyme. Immunostaining patterns within the duodenal epithelium for lactase differed from sucrase-isomaltase in adjacent sections, illustrating independent regulation at the cellular level.

Conclusions: In the duodenum of white children, lactase and sucrase-isomaltase seem primarily regulated at the transcriptional level. The expression of each enzyme in the intestinal epithelium is regulated by an independent mechanism. Lactase and sucrase-isomaltase exhibit stable mRNA and protein levels in healthy children as they grow to adulthood. Mucosal damage affected levels of both enzymes negatively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Aging
  • Antibodies, Monoclonal
  • Atrophy
  • Biopsy
  • Child
  • Child, Preschool
  • Duodenum / enzymology*
  • Gene Expression Regulation, Enzymologic*
  • Humans
  • Immunohistochemistry
  • Infant
  • Intestinal Mucosa / enzymology
  • Intestinal Mucosa / pathology
  • Lactase
  • Prospective Studies
  • RNA, Messenger / metabolism
  • Sucrase-Isomaltase Complex / genetics*
  • beta-Galactosidase / genetics*

Substances

  • Antibodies, Monoclonal
  • RNA, Messenger
  • Sucrase-Isomaltase Complex
  • Lactase
  • beta-Galactosidase