Wegener's granulomatosis: anti-proteinase 3 antibodies are potent inductors of human endothelial cell signaling and leakage response

• Published in: The Journal of experimental medicine 1998-02, Vol.187 (4), p.497-503
• Main Authors: Sibelius, U, Hattar, K, Schenkel, A, Noll, T, Csernok, E, Gross, W L, Mayet, W J, Piper, H M, Seeger, W, Grimminger, F
• Format: Article
• Language: English
• Subjects: Antibodies, Antineutrophil Cytoplasmic - immunology; Antibodies, Monoclonal - immunology; Cell Communication; Cells, Cultured; E-Selectin - metabolism; Endothelium, Vascular - drug effects; Endothelium, Vascular - immunology; Endothelium, Vascular - pathology; Enzyme-Linked Immunosorbent Assay; Granulomatosis with Polyangiitis - immunology; Granulomatosis with Polyangiitis - pathology; Humans; Myeloblastin; Phosphatidylinositols - metabolism; Platelet Activating Factor - metabolism; Polymerase Chain Reaction; Serine Endopeptidases - immunology; Signal Transduction; Tumor Necrosis Factor-alpha - pharmacology; Vascular Cell Adhesion Molecule-1 - metabolism
• ISSN: 0022-1007; 1540-9538
• DOI: 10.1084/jem.187.4.497

Anti-neutrophil cytoplasmic antibodies (ANCAs) targeting proteinase 3 (PR3) have a high specifity for Wegener's granulomatosis (WG), and their role in activating leukocytes is well appreciated. In this study, we investigated the influence of PR3-ANCA and murine monoclonal antibodies on human umbilical vascular endothelial cells (HUVECs). Priming of HUVECs with tumor necrosis factor alpha induced endothelial upregulation of PR3 message and surface expression of this antigen, as measured by Cyto-ELISA, with a maximum occurrence after 2 h. Primed cells responded to low concentrations of both antibodies (25 ng-2.5 microg/ml), but not to control immunoglobulins, with pronounced, dose-dependent phosphoinositide hydrolysis, as assessed by accumulation of inositol phosphates. The signaling response peaked after 20 min, in parallel with the appearance of marked prostacyclin and platelet-activating factor synthesis. The F(ab)2 fragment of ANCA was equally potent as ANCA itself. Disrupture of the endothelial F-actin content by botulinum C2 toxin to avoid antigen-antibody internalization did not affect the response. In addition to the metabolic events, anti-PR3 challenge, in the absence of plasma components, provoked delayed, dose-dependent increase in transendothelial protein leakage. We conclude that anti-PR3 antibodies are potent inductors of the preformed phosphoinositide hydrolysis-related signal tranduction pathway in human endothelial cells. Associated metabolic events and the loss of endothelial barrier properties suggest that anti-PR3-induced activation of endothelial cells may contribute to the pathogenetic sequelae of autoimmune vasculitis characterizing WG.