Literature DB >> 1951625

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.

C Eldredge1, S Merritt, M Goyal, H Kulaga, T J Kindt, R Wiggins.   

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.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1951625      PMCID: PMC1886351     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  59 in total

1.  The significance of extracapillary proliferation. Clinicopathological review of 60 patients.

Authors:  J A Whitworth; L Morel-Maroger; F Mignon; G Richet
Journal:  Nephron       Date:  1976       Impact factor: 2.847

2.  Goodpasture's syndrome: an analysis of 29 cases.

Authors:  C A Teague; P B Doak; I J Simpson; S P Rainer; P B Herdson
Journal:  Kidney Int       Date:  1978-06       Impact factor: 10.612

3.  Cellular aspects of rabbit Masugi nephritis. II. Progressive glomerular injuries with crescent formation.

Authors:  Y Kondo; H Shigematsu; Y Kobayashi
Journal:  Lab Invest       Date:  1972-12       Impact factor: 5.662

4.  Rapidly progressive glomerulonephritis with antibodies against glomerular basement membranes in serum and kidneys.

Authors:  R Berg; A Bergstrand; J Bergström; R Cunningham; C Tagesson; J Wasserman
Journal:  Clin Nephrol       Date:  1976-01       Impact factor: 0.975

5.  Analysis of alpha 1 (I) procollagen alpha 1 (IV) collagen, and beta-actin mRNA in glomerulus and cortex of rabbits with experimental anti-glomerular basement membrane disease. Evidence for early extraglomerular collagen biosynthesis.

Authors:  S E Merritt; P D Killen; S H Phan; R C Wiggins
Journal:  Lab Invest       Date:  1990-12       Impact factor: 5.662

6.  Histology of human tubulo-interstitial nephritis associated with antibodies to renal basement membranes.

Authors:  G Andres; J Brentjens; R Kohli; R Anthone; S Anthone; T Baliah; M Montes; B K Mookerjee; A Prezyna; M Sepulveda; R Venuto; C Elwood
Journal:  Kidney Int       Date:  1978-06       Impact factor: 10.612

7.  The origin of glomerular crescents in experimental nephrotoxic serum nephritis in the rabbit.

Authors:  V Cattell; S W Jamieson
Journal:  Lab Invest       Date:  1978-12       Impact factor: 5.662

8.  Intraglomerular T cells and monocytes in nephritis: study with monoclonal antibodies.

Authors:  F E Nolasco; J S Cameron; B Hartley; A Coelho; G Hildreth; R Reuben
Journal:  Kidney Int       Date:  1987-05       Impact factor: 10.612

9.  The role of the interstitium of the renal cortex in renal disease.

Authors:  A Bohle; H Christ; K E Grund; S Mackensen
Journal:  Contrib Nephrol       Date:  1979       Impact factor: 1.580

10.  Evidence for a pathogenic role of a cell-mediated immune mechanism in experimental glomerulonephritis.

Authors:  A K Bhan; E E Schneeberger; A B Collins; R T McCluskey
Journal:  J Exp Med       Date:  1978-07-01       Impact factor: 14.307

View more
  2 in total

1.  Tissue factor initiates glomerular fibrin deposition and promotes major histocompatibility complex class II expression in crescentic glomerulonephritis.

Authors:  J H Erlich; S R Holdsworth; P G Tipping
Journal:  Am J Pathol       Date:  1997-03       Impact factor: 4.307

Review 2.  The inflammatory function of renal glomerular mesangial cells and their interaction with the cellular immune system.

Authors:  H H Radeke; K Resch
Journal:  Clin Investig       Date:  1992-09
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.