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Expression of platelet-derived growth factor receptors is induced on connective tissue cells during chronic synovial inflammation.

Abstract
The tissue distribution of the receptor for platelet-derived growth factor (PDGF) was investigated by immunohistochemistry on frozen sections from normal and inflamed synovial tissue using monoclonal antibodies to the receptor. Non-inflamed synovial tissue showed no staining, indicating that PDGF receptor expression is low or absent in normal tissue. In contrast, tissue from synovitis with prominent neovascularization showed a strong staining in the tunica media of the proliferating blood vessels as well as on connective tissue cells in the stroma. Tissue from synovitis with prominent proliferation of synovial lining showed intense staining for PDGF receptors in fibroblast-like cells of the lining and a less intense staining on vascular and connective tissue cells deeper in the stroma. Staining for PDGF receptors was also intense in the pannus tissue close to infiltrated bone and cartilage. In all these forms of synovitis, PDGF receptor staining was associated with increased HLA-DR staining and infiltration of macrophages and T lymphocytes. The finding that PDGF receptor expression is induced in conjunction with the chronic synovial inflammation associated with rheumatoid arthritis and some other forms of arthritides suggests that PDGF may play a role in the stimulation of mesenchymal cell proliferation that often accompanies chronic inflammatory disease.
AuthorsK Rubin, L Terracio, L Rönnstrand, C H Heldin, L Klareskog
JournalScandinavian journal of immunology (Scand J Immunol) Vol. 27 Issue 3 Pg. 285-94 (Mar 1988) ISSN: 0300-9475 [Print] England
PMID2451272 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Platelet-Derived Growth Factor
  • Receptors, Cell Surface
  • Receptors, Platelet-Derived Growth Factor
Topics
  • Chronic Disease
  • Connective Tissue (metabolism, pathology)
  • Fluorescent Antibody Technique
  • Frozen Sections
  • Humans
  • Platelet-Derived Growth Factor (metabolism, physiology)
  • Receptors, Cell Surface (analysis, biosynthesis, immunology)
  • Receptors, Platelet-Derived Growth Factor
  • Staining and Labeling
  • Synovitis (metabolism, pathology)

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