Analysis of T cells and major histocompatibility complex class I and class II mRNA and protein content and distribution in antiglomerular basement membrane disease in the rabbit

Am J Pathol. 1991 Nov;139(5):1021-35.

Abstract

The major interacting components of the immune system, major histocompatibility complex (MHC) class I and class II proteins and T cells were analyzed in a model of anti-GBM (glomerular basement membrane) disease in the rabbit that progresses to develop cellular crescents and glomerular and interstitial fibrosis. Class I and II mRNA and protein were measured in isolated glomeruli and whole renal cortex using cDNA probes and monoclonal antibodies. The distribution of T cells and class I and II proteins was assessed by immunofluorescence. Normal glomeruli contained no T cells and were class II negative. By day 4, glomeruli contained MHC class I and II mRNA and protein and class II positive T cells. Although some animals had T cells in the periglomerular area, these cells were class II negative. By day 7 periglomerular T cells were largely class II positive (activated) and there was increased MHC class I and II mRNA and protein in whole renal cortex. Later T cells accumulated in the tubulo-interstitial compartment, which became diffusely positive for MHC classes I and II, but to a variable extent in different animals. Those with high class II mRNA expression also had detectable T cell antigen receptor mRNA by Northern analysis. The authors conclude 1) in this model there was a close association between mRNA abundance and protein expression for both MHC classes I and II in glomeruli and renal cortex as a whole; 2) in this model of glomerular injury there are three phases of activation. The first phase takes place in the glomerulus and is associated with accumulation of activated T cells and MHC class I and II protein in the glomerulus. Phase 2 is associated with the accumulation of periglomerular T cells and their becoming class II positive. There is subsequent dissemination (phase 3) of activated T cells and accumulation of class I and II mRNA and protein throughout the interstitial compartment. This spacial progression of glomerulocentric inflammation is likely associated with degree of injury and permanent loss of renal function.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Blotting, Northern
  • Blotting, Western
  • DNA / genetics
  • DNA Probes
  • Disease Models, Animal
  • Fluorescent Antibody Technique
  • Gene Expression / genetics
  • Glomerulonephritis, Membranous / genetics
  • Glomerulonephritis, Membranous / immunology
  • Glomerulonephritis, Membranous / pathology*
  • Histocompatibility Antigens Class I / analysis*
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class II / analysis
  • Histocompatibility Antigens Class II / genetics*
  • Kidney Cortex / chemistry
  • Kidney Cortex / pathology
  • Kidney Glomerulus / chemistry
  • Kidney Glomerulus / pathology
  • Lymphocyte Activation / immunology
  • Nucleic Acid Hybridization
  • RNA, Messenger / analysis*
  • RNA, Messenger / genetics
  • Rabbits
  • Receptors, Antigen, T-Cell / analysis
  • Receptors, Antigen, T-Cell / genetics
  • T-Lymphocytes / chemistry
  • T-Lymphocytes / pathology*

Substances

  • Antibodies, Monoclonal
  • DNA Probes
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • RNA, Messenger
  • Receptors, Antigen, T-Cell
  • DNA