Literature DB >> 7681715

Intercellular adhesion molecules in normal synovium.

K Fairburn1, M Kunaver, L S Wilkinson, G Cambridge, D Haskard, J C Edwards.   

Abstract

The vasculature of normal synovium and skin has been examined for the presence of molecules believed to be involved in intercellular adhesion and whose expression on endothelial cells in vitro is known to be upregulated by cytokines. Synovium was obtained from clinically and histologically normal joints removed during amputations for proximal sarcomata. Skin was obtained from healthy volunteers. Cryostat sections of tissues were assessed by immunohistochemistry and microdensitometry for the presence of E-selectin using monoclonal antibody 1.2B6, intercellular adhesion molecule-1 (ICAM-1) using monoclonal antibody 6.5B5 and vascular cell adhesion molecule (VCAM-1) using monoclonal antibody 1.4C3. Both E-selectin and ICAM-1 were present on a proportion of normal synovial venules but at a level comparable to or lower than that found on dermal vessels. (Staining intensities given as mean absorption indices: superficial synovium 1.2B6: 9.9 +/- 11.4, 6.5B5: 10.2 +/- 12.0, deep synovium 1.2B6: 6.6 +/- 9.9, 6.5B5: 24.6 +/- 15.7, skin 1.2B6: 13.1 +/- 16.6, 6.5B5: 36.4 +/- 12.9.) E-selectin expression was most prominent on small superficial venules in synovium and ICAM-1 most strongly expressed on larger, deep venules. VCAM-1 was found at low levels on cells associated with vessel walls but no significant endothelial staining was seen in either type of tissue. VCAM-1 was also present on cells of the synovial lining layer. Some of the findings in synovium could have been attributable to tumour related cytokine release, but the consistency of findings and comparability to skin suggest that this is relatively unlikely.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1993        PMID: 7681715     DOI: 10.1093/rheumatology/32.4.302

Source DB:  PubMed          Journal:  Br J Rheumatol        ISSN: 0263-7103


  4 in total

1.  Neovascularisation and the induction of cell adhesion molecules in response to degradation products from orthopaedic implants.

Authors:  N al-Saffar; J T Mah; Y Kadoya; P A Revell
Journal:  Ann Rheum Dis       Date:  1995-03       Impact factor: 19.103

2.  Adhesion molecule expression and complement activation in vessel walls in synovial tissue from patients with chronic inflammatory joint disease.

Authors:  O J Mellbye; Y Shen; K Høgåsen; T E Mollnes; O Førre
Journal:  Clin Rheumatol       Date:  1996-09       Impact factor: 2.980

3.  Microarchitecture and protective mechanisms in synovial tissue from clinically and arthroscopically normal knee joints.

Authors:  M D Smith; E Barg; H Weedon; V Papengelis; T Smeets; P P Tak; M Kraan; M Coleman; M J Ahern
Journal:  Ann Rheum Dis       Date:  2003-04       Impact factor: 19.103

4.  The formation of human synovial joint cavities: a possible role for hyaluronan and CD44 in altered interzone cohesion.

Authors:  J C Edwards; L S Wilkinson; H M Jones; P Soothill; K J Henderson; J G Worrall; A A Pitsillides
Journal:  J Anat       Date:  1994-10       Impact factor: 2.610

  4 in total

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