Open AccessInhibition of systemic sclerosis dermal fibroblast type I collagen production and gene expression by simvastatin
Author(s) -
Louneva Natalia,
Huaman Gonzalo,
Fertala Joanna,
Jiménez Sergio A.
Publication year - 2006
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.21723
Subject(s) - simvastatin , geranylgeranyl pyrophosphate , dermal fibroblast , gene expression , mevalonate pathway , type i collagen , fibroblast , microbiology and biotechnology , statin , biology , cell culture , chemistry , endocrinology , gene , biochemistry , prenylation , enzyme , biosynthesis , genetics
Abstract Objective To examine whether statins are capable of modulating collagen gene expression in cultured systemic sclerosis dermal fibroblasts. Methods Cultured dermal fibroblasts from 3 patients with diffuse systemic sclerosis of recent onset were treated with 5 μ M and 10 μ M of simvastatin for 3 or 4 days. Morphologic features, cytotoxicity, and type I collagen production and messenger RNA (mRNA) levels in the fibroblasts were examined. The effects of mevalonate, geranylgeranyl pyrophosphate (GGPP), and farnesyl pyrophosphate (FPP), which are lipids downstream from the hydroxymethylglutaryl–coenzyme A block, were also examined. Transient transfections with COL1A1 promoter‐reporter constructs and electrophoretic gel mobility shift assays were utilized to examine COL1A1 transcription and Sp1 and CCAAT‐box binding factor (CBF) binding. Results Simvastatin did not cause morphologic changes or cytotoxicity in the fibroblasts, even after 4 days of treatment. Type I collagen production and mRNA levels showed a potent and dose‐related inhibition following 3 and 4 days of treatment. The inhibition of collagen gene expression by simvastatin was completely reversed by mevalonate and GGPP, but not by FPP. The statin effects occurred at the transcriptional level and involved the proximal COL1A1 promoter region encompassing −174 bp. A significant reduction in Sp1 and CBF binding activity was also found in simvastatin‐treated cells. Conclusion Simvastatin is a powerful inhibitor of type I collagen gene expression in normal and systemic sclerosis fibroblasts. The pleiotropic protective effects of statins on various endothelial and immune cell functions in conjunction with their potent inhibitory effects on type I collagen gene expression suggest that statins may be effective therapeutic agents in systemic sclerosis.