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Título

Expression of the peptide C4b-binding protein {beta} in the arthritic joint

AutorSánchez-Pernaute, Olga; Esparza-Gordillo, Jorge CSIC; Largo, Raquel; Calvo, Emilio; Álvarez-Soria, María Ángeles; Marcos, M. Esther; Herrero-Beaumont, Gabriel; Rodríguez de Córdoba, Santiago
Fecha de publicaciónoct-2006
EditorBMJ Publishing Group
CitaciónAnnals of the Rheumatic Diseases 65(10):1279-1285(2006)
ResumenBackground: C4b-binding protein (C4BP) is a plasma oligomeric glycoprotein that participates in the regulation of complement and haemostasis. Complement-regulatory activity depends on the C4BPα-polypeptide, whereas the C4BPβ-polypeptide inactivates protein S, interfering with the anti-coagulatory protein C-dependent pathway. Objective: To investigate the expression of C4BPβ in the rheumatoid joint. Methods: Expression of C4BP was studied in synovial explants from patients with rheumatoid arthritis, osteoarthritis and healthy controls, using immunohistochemistry and in situ hybridisation. C4BP isoforms and free C4BPβ were studied in synovial effusions from patients with rheumatoid arthritis, osteoarthritis and microcrystalline arthritis (MCA) by immunoblotting; total and free protein S levels were studied by enzyme immunoassay. Results: C4BPβ was overexpressed in the synovial membranes of patients with rheumatoid arthritis, in close association with the severity of synovitis and the extension of interstitial fibrin deposits. As many as 85% fluids from patients with rheumatoid arthritis contained free C4BPβ, whereas this unusual polypeptide was present in 50% fluids from patients with MCA and 40% fluids from patients with osteoarthritis. Free protein S at the effusions was pathologically reduced in patients with rheumatoid arthrits and MCA, and remained normal in patients with osteoarthritis. Conclusion: C4BPβ is expressed by the inflamed synovial tissue, where it can participate in processes of tissue remodelling associated with invasive growth
Descripción7 páginas, 6 figuras -- PAGS nros. 1279-1285
Versión del editorhttp:dx.doi.org/10.1136/ard.2006.052118
URIhttp://hdl.handle.net/10261/69834
DOI10.1136/ard.2006.052118
ISSN0003-4967
E-ISSN1468-2060
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