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Urokinase, a constitutive component of the inflamed synovial fluid, induces arthritis.

Journal article
Authors Tao Jin
Andrej Tarkowski
Peter Carmeliet
Maria Bokarewa
Published in Arthritis research & therapy
Volume 5
Issue 1
Pages R9-R17
ISSN 1478-6362
Publication year 2003
Published at Institute of Internal Medicine, Dept of Rheumatology and Inflammation Research
Pages R9-R17
Language en
Links www.ncbi.nlm.nih.gov/entrez/query.f...
Keywords Adult, Aged, Animals, Arthritis, chemically induced, immunology, pathology, Arthritis, Rheumatoid, enzymology, Cells, Cultured, Cytokines, biosynthesis, Female, Humans, Injections, Intra-Articular, Lymphocytes, immunology, Mice, Mice, SCID, Middle Aged, Monocytes, immunology, Synovial Fluid, enzymology, Urokinase-Type Plasminogen Activator, administration & dosage, metabolism, toxicity
Subject categories Rheumatology and Autoimmunity

Abstract

Urokinase plasminogen activator (uPA) is an important regulator of fibrinolysis in synovial fluid. An increase of uPA activity and expression of its receptor have been reported in joints of patients with rheumatoid arthritis (RA). The aim of the present study was to assess the arthritogenic capacity of uPA and the mechanisms by which this effect is mediated. uPA was injected into the knee joints of healthy mice, and morphological signs of arthritis were assessed 4 days after the injection. The prerequisite of different leukocyte populations for the development of uPA-triggered arthritis was assessed by selective cell depletion. The inflammatory capacity of uPA was assessed in vitro. Finally, levels of uPA were measured in 67 paired blood and synovial fluid samples from RA patients. The synovial fluid from RA patients displayed higher levels of uPA compared with blood samples. Morphological signs of arthritis were found in 72% of uPA-injected joints compared with in only 18% of joints injected with PBS (P < 0.05). Synovitis was characterised by infiltration of CD4-Mac-1+ mononuclear cells, by the formation of pannus and by occasional cartilage destruction. The absence of monocytes and lymphocytes diminished the frequency of synovitis (P < 0.01), indicating an arthritogenic role of both these leukocyte populations. Synthetic uPA inhibitor downregulated the incidence of uPA-triggered arthritis by 50%. uPA induced arthritis, stimulating the release of proinflammatory cytokines IL-6, IL-1beta and tumour necrosis factor alpha. Accumulation of uPA locally in the joint cavity is a typical finding in erosive RA. uPA exerts potent arthritogenic properties and thus may be viewed as one of the essential mediators of joint inflammation.

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