Endothelin and sex hormones modulate the fibronectin synthesis by cultured human skin scleroderma fibroblasts
- S Soldano1,
- P Montagna1,
- B Villaggio2,
- A Parodi3,
- G Gianotti3,
- A Sulli1,
- B Seriolo1,
- M E Secchi1,
- M Cutolo1
- 1Research Laboratories and Clinical Academic Unit of Rheumatology, Department of Internal Medicine, University of Genova, Italy
- 2Research Laboratories and Clinical Academic Unit of Nephrology, University of Genova, Italy
- 3Department of Endocrinological and Medical Science, Unit of Dermatology, University of Genova, Italy
- M Cutolo, Research Laboratories and Clinical Academic Unit of Rheumatology, Department of Internal Medicine, University of Genova, Viale Benedetto XV, 6, 16132 Genova, Italy; mcutolo{at}unige.it
- Accepted 5 October 2008
- Published Online First 24 October 2008
Abstract
Objective: To evaluate the influence of endothelin-1 (ET-1) and sex hormones on cell proliferation and extracellular matrix (ECM) synthesis (ie, fibronectin, laminin) by cultured normal and scleroderma (SSc) human skin fibroblasts (FBs).
Methods: Primary cultures of FBs were treated with ET-1 and sex hormones (17β-oestradiol or testosterone) for 24 h. Cell growth was analysed by methiltetrazolium salt test, ECM synthesis was evaluated by immunocytochemistry and western blot, both at 24 h.
Results: In normal FBs, ET-1 and 17β-oestradiol, as well as their combination, increased cell growth (p<0.001, p<0.001, p<0.01 vs untreated cells (control), respectively) and fibronectin synthesis (p<0.05, p<0.05, p<0.01 vs control, respectively). By contrast, testosterone either alone or in combination with ET-1 did not influence cell proliferation, but decreased fibronectin synthesis (p<0.05, testosterone vs control). In SSc FBs, ET-1 and 17β-oestradiol alone or their combination induced an increased fibronectin synthesis (p<0.05, p<0.05, p<0.01 vs control, respectively). Unexpectedly, testosterone induced an increase of fibronectin synthesis (p<0.05 vs control).
Conclusions: ET-1 and 17β-oestradiol seem to exert a profibrotic effect in normal and SSc culture FBs and might suggest their synergistic effect in the pathogenesis of the fibrotic process in SSc.
Footnotes
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Competing interests: None declared.
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Ethics approval: Informed consent and ethical committee approval was obtained.








