IL-1 mRNA expression detected by in situ hybridization and polymerase chain reaction in human thymus and thymoma. Correlation with late T-cell maturation in normal versus neoplastic thymus

Thymus. 1993 Aug;22(1):45-54.

Abstract

Interleukin-1 has long been suggested to participate in the development of T-cells in the thymus. To determine whether IL-1 was produced in the human thymus, we used the technique of in situ hybridization and PCR amplification of mRNA. High levels of IL-1 mRNA were detected in cells at the cortico-medullary border, which separates immature from mature T-cells, suggesting a role for IL-1 in a late stage in T-cell maturation. IL-1 transcripts were detectable by a single step PCR reaction in these samples. We examined a series thymomas (human thymic epithelial tumors) that induce partial T-cell maturation: In this group of thymomas T-cells develop to the cortical stage but not beyond. We failed to detect high levels of IL-1 mRNA expression in these tumors by in-situ hybridization, IL-1 mRNA was detected only in one of these samples by a single step PCR amplification. However, all of the samples were positive, when analyzed with a more sensitive, two step amplification of IL-1 mRNA by the use of nested primers. These results are consistent with the hypothesis that higher level of IL-1 expression is either the consequence of, or required for late T-cell maturation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Base Sequence
  • Cell Differentiation
  • Child, Preschool
  • Gene Expression Regulation*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • In Situ Hybridization
  • Infant
  • Interleukin-1 / biosynthesis
  • Interleukin-1 / genetics*
  • Middle Aged
  • Molecular Sequence Data
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Proteins / genetics
  • Polymerase Chain Reaction
  • RNA, Messenger / biosynthesis*
  • RNA, Neoplasm / biosynthesis*
  • T-Lymphocytes / cytology*
  • Thymoma / metabolism*
  • Thymus Gland / metabolism*
  • Thymus Neoplasms / metabolism*

Substances

  • Interleukin-1
  • Neoplasm Proteins
  • RNA, Messenger
  • RNA, Neoplasm