Antiangiogenic VEGF Isoform in Inflammatory Myopathies. (11th June 2013)

• Record Type: Journal Article
• Authors: Volpi, Nila; Pecorelli, Alessandra; Lorenzoni, Paola; Di Lazzaro, Francesco; Belmonte, Giuseppe; Aglianò, Margherita; Cantarini, Luca; Giannini, Fabio; Grasso, Giovanni; Valacchi, Giuseppe
• Other Names: Ruth Jeffrey H. Academic Editor.
• Is Part Of: Mediators of inflammation. Volume 2013(2013)
• Publication Date: 2013-06-11
• Subjects: Inflammation -- Mediators -- Periodicals; Biological response modifiers -- Periodicals; Inflammation (Pathologie) -- Médiateurs; Immunomodulateurs; Biological response modifiers; Inflammation -- Mediators; Immunology; Autacoids; Immunologic Factors; Cell Adhesion Molecules; Cell Communication; Cytokines; Inflammation; Periodicals; Electronic journals; 616.0473
• DOI: 10.1155/2013/219313
• Languages: English
• ISSNs: 0962-9351

Abstract

Abstract : Objective . To investigate expression of vascular endothelial growth factor (VEGF) antiangiogenic isoform A - 165 b on human muscle in idiopathic inflammatory myopathies (IIM) and to compare distribution of angiogenic/antiangiogenic VEGFs, as isoforms shifts are described in other autoimmune disorders. Subjects and Methods . We analyzed V E G F - A 165 b and VEGF-A by western blot and immunohistochemistry on skeletal muscle biopsies from 21 patients affected with IIM (polymyositis, dermatomyositis, and inclusion body myositis) and 6 control muscle samples. TGF- β, a prominent VEGF inductor, was analogously evaluated. Intergroup differences of western blot bands density were statistically examined. Endomysial vascularization, inflammatory score, and muscle regeneration, as pathological parameters of IIM, were quantitatively determined and their levels were confronted with VEGF expression. Results . V E G F - A 165 b was significantly upregulated in IIM, as well as TGF- β . VEGF-A was diffusely expressed on unaffected myofibers, whereas regenerating/atrophic myofibres strongly reacted for both VEGF-A isoforms. Most inflammatory cells and endomysial vessels expressed both isoforms. V E G F - A 165 b levels were in positive correlation to inflammatory score, endomysial vascularization, and TGF- β . Conclusions . Our findings indicate skeletal muscle expression of antiangiogenic V E G F - A 165 b and preferential upregulation in IIM, suggesting that modulation of VEGF-A isoforms may occur in myositides.