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Imatinib mesylate inhibits platelet derived growth factor stimulated proliferation of rheumatoid synovial fibroblasts.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2006 Aug 18; Vol. 347 (1), pp. 31-5. Date of Electronic Publication: 2006 Jun 21. - Publication Year :
- 2006
-
Abstract
- Synovial fibroblast is the key cell type in the growth of the pathological synovial tissue in arthritis. Here, we show that platelet-derived growth factor (PDGF) is a potent mitogen for synovial fibroblasts isolated from patients with rheumatoid arthritis. Inhibition of PDGF-receptor signalling by imatinib mesylate (1muM) completely abrogated the PDGF-stimulated proliferation and inhibited approximately 70% of serum-stimulated proliferation of synovial fibroblasts. Similar extent of inhibition was observed when PDGF was neutralized with anti-PDGF antibodies, suggesting that imatinib mesylate does not inhibit pathways other than those mediated by PDGF-receptors. No signs of apoptosis were detected in synovial fibroblasts cultured in the presence of imatinib. These results suggest that imatinib mesylate specifically inhibits PDGF-stimulated proliferation of synovial fibroblasts, and that inhibition of PDGF-receptors could represent a feasible target for novel antirheumatic therapies.
- Subjects :
- Arthritis, Rheumatoid physiopathology
Benzamides
Cell Proliferation drug effects
Cells, Cultured
Dose-Response Relationship, Drug
Drug Combinations
Humans
Imatinib Mesylate
Protein Kinase Inhibitors administration & dosage
Synovial Membrane drug effects
Arthritis, Rheumatoid pathology
Fibroblasts drug effects
Fibroblasts pathology
Piperazines administration & dosage
Platelet-Derived Growth Factor administration & dosage
Pyrimidines administration & dosage
Synovial Membrane pathology
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 347
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 16806061
- Full Text :
- https://doi.org/10.1016/j.bbrc.2006.06.052