Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/22454
Title: Imatinib mesylate inhibits in vitro and ex vivo biologic responses related to vascular occlusion in giant cell arteritis.
Author: Lozano García, Ester
Segarra Blasco, Marta
García Martínez, Ana
Hernández Rodríguez, José
Cid Xutglà, M. Cinta
Keywords: Arteritis de cèl·lules gegants
Vasos sanguinis
Factors de creixement
Giant cell arteritis
Blood-vessels
Growth factors
Issue Date: 2007
Publisher: BMJ Group
Abstract: Objectives: Ischaemic complications occur in 15–20% of patients with giant cell arteritis (GCA). The aim of our study was to explore the effect of mesenchymal growth factors expressed in GCA lesions on myointimal cell responses related to the development of intimal hyperplasia and vessel occlusion.#N##N#Methods: We developed a method to obtain primary human temporal artery derived myointimal cells (HTAMCs) based on the culture of temporal artery sections on Matrigel.#N##N#Results: Among the factors tested (platelet-derived growth factor (PDGF)-AB, fibroblast growth factor (FGF)-2, vascular endothelial growth factor (VEGF), epidermal growth factor (EGF), transforming growth factor (TGF)β, chemokine (C-C motif) ligand (CCL)2, interleukin (IL)6 and IL1β), PDGF exhibited the strongest activity in inducing HTAMC proliferation and migration. As assessed by protein array, immunoassay and quantitative real-time reverse transcriptase (RT)-PCR, PDGF stimulated matrix proteins (collagen I, collagen III and fibronectin) as well as CCL2 and angiogenin production by HTAMCs. Imatinib mesylate inhibited PDGF-mediated activation of signalling pathways (Src, extracellular signal-regulated kinase (ERK) and Akt phosphorylation) related to cell motility and survival, efficiently resulting in inhibition of PDGF-induced HTAMC responses. Myointimal cell outgrowth from cultured temporal artery sections from patients with GCA, where multiple interactions take place, was also efficiently reduced by imatinib.#N##N#Conclusion: Among several mediators produced in GCA, PDGF has the highest vaso-occlusive potential. PDGF may also contribute to disease perpetuation by stimulating the production of angiogenic factors (angiogenin) and chemoattractants (CCL2). Imatinib mesylate strongly inhibits PDGF-mediated responses, suggesting a therapeutic potential to limit vascular occlusion and ischaemic complications in large vessel vasculitis.
Note: Reproducció digital del document publicat a: http://dx.doi.org/10.1136/ard.2007.070805
It is part of: Annals of the Rheumatic Diseases, 2008, vol. 67, núm. 11, p. 1581-1588
Related resource: http://dx.doi.org/10.1136/ard.2007.070805
URI: http://hdl.handle.net/2445/22454
ISSN: 0003-4967
Appears in Collections:Articles publicats en revistes (Medicina)

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