Differing patterns of transforming growth factor-beta expression in normal intestinal mucosa and in active celiac disease

J Pediatr Gastroenterol Nutr. 1999 Sep;29(3):308-13. doi: 10.1097/00005176-199909000-00013.

Abstract

Background: Growth-inhibitory autocrine polypeptides such as transforming growth factor (TGF)-beta may play a role in the control of normal epithelial cell proliferation and differentiation. In addition, TGF-beta has a central role in extracellular matrix homeostasis and regulates the immune response at the local level. In this study immunohistochemistry was used to examine the pattern of TGF-beta protein distribution and quantitative reverse transcription-polymerase chain reaction (RT-PCR) to determine levels of TGF-beta messenger RNA expression in normal intestinal mucosa and in the flat mucosa of children with celiac disease.

Methods: Small intestinal biopsies were performed in children with active celiac disease and in histologically normal control subjects. Frozen sections were single stained using an anti-TGF-beta monoclonal antibody and were double stained for TGF-beta and T cell, macrophages, and the activation marker CD25. Total RNA was extracted from frozen specimens and competitive quantitative RT-PCR performed for TGF-beta mRNA using internal synthetic standard RNA.

Results: In normal intestinal mucosa, by immunohistochemistry, TGF-beta expression was most prominent in the villous tip epithelium, whereas in the lamina propria, weak immunoreactivity was present. The celiac mucosa showed weak and patchy epithelial TGF-beta immunoreactivity. In contrast, an intense staining positivity was present in the lamina propria localized mostly in the subepithelial region where T cells, macrophages, and CD25+ cells were detected by double staining. By quantitative RT-PCR, levels of TGF-beta mRNA transcripts appeared to be increased in celiac intestinal mucosa compared with that in control subjects, although the difference did not reach statistical significance.

Conclusions: These observations suggest that TGF-beta expression is associated with differentiated enterocyte function. In celiac disease the lower TGF-beta epithelial cell expression could be a consequence of the preponderance of a less differentiated epithelial cell phenotype also present in the surface epithelium. In contrast, the prominent TGF-beta positivity of the subepithelial lamina propria suggests an association with the local immune and inflammatory response, as well as a potential role of these peptides in mesenchymal-epithelial cell interaction.

MeSH terms

  • Antigens, CD / analysis
  • Antigens, Differentiation, Myelomonocytic / analysis
  • Biopsy
  • CD3 Complex / analysis
  • Celiac Disease / metabolism*
  • Celiac Disease / pathology
  • Child
  • Child, Preschool
  • Female
  • Gene Expression*
  • Humans
  • Immunohistochemistry
  • Intestinal Mucosa / chemistry*
  • Intestinal Mucosa / pathology
  • Lymphocytes / immunology
  • Lymphocytes / pathology
  • Macrophages / immunology
  • Macrophages / pathology
  • Male
  • RNA, Messenger / analysis
  • Receptors, Interleukin-2 / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • T-Lymphocytes / immunology
  • T-Lymphocytes / pathology
  • Transforming Growth Factor beta / analysis
  • Transforming Growth Factor beta / genetics*

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD3 Complex
  • CD68 antigen, human
  • RNA, Messenger
  • Receptors, Interleukin-2
  • Transforming Growth Factor beta