Tumor necrosis factor-alpha induction of major histocompatibility complex class II antigen expression is inhibited by interferon-gamma in a monocytic cell line

Eur J Immunol. 1995 Nov;25(11):3202-6. doi: 10.1002/eji.1830251134.

Abstract

Regulation of major histocompatibility complex (MHC) class II antigen expression by cytokines has been suggested to play a major role in the initiation and propagation of immune and autoimmune processes. The analysis of class II gene regulation benefits greatly from the existence of mutants with defects in regulatory factors. We report the establishment of a subclone of the human monocytic cell line U937, termed C119/9, with unusual cytokine regulation of MHC class II expression. In contrast to the parental U937 cell line, only tumor necrosis factor (TNF)-alpha, and not interferon (IFN)-gamma induces the expression of MHC class II antigens on C119/9 cells, and paradoxically, this induction was inhibited almost completely by IFN-gamma. The HLA-DR induction is controlled at the transcriptional level by the first 150 bp of the class II promoter which contains all the class II consensus elements. Both HLA-DR and -DQ mRNA are induced by TNF-alpha treatment, and both are diminished upon co-treatment with TNF-alpha and IFN-gamma. This antagonism between TNF-alpha and IFN-gamma seem to be restricted to MHC class II genes. This subline of U937 cells may be useful in further studies of MHC class II regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Northern
  • Chloramphenicol O-Acetyltransferase / analysis
  • Clone Cells
  • Down-Regulation / drug effects
  • HLA-DR Antigens / biosynthesis*
  • HLA-DR Antigens / genetics
  • Humans
  • Interferon-gamma / pharmacology*
  • Leukemia, Promyelocytic, Acute
  • RNA, Messenger / analysis
  • Receptors, IgG / biosynthesis
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors*

Substances

  • HLA-DR Antigens
  • RNA, Messenger
  • Receptors, IgG
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Chloramphenicol O-Acetyltransferase