Selected Works of Sergio Jiménez, MD, MACR
Role of protein kinase C-delta in the regulation of collagen gene expression in scleroderma fibroblasts
Sergio A. Jimenez, Thomas Jefferson University; Svetlana Gaidarova, Thomas Jefferson University; Biagio Saitta, Thomas Jefferson University; Nora Sandorfi, Thomas Jefferson University; David J. Herrich, University of Pennsylvania; Joan C. Rosenbloom, University of Pennsylvania; Umberto Kucich, University of Pennsylvania; William R. Abrams, University of Pennsylvania; and Joel Rosenbloom, University of Pennsylvania
DATE: November 2001
SOURCE: Journal of Clinical Investigation, 108:1395-1403
RELATED URL: http://www.jci.org/articles/view/12347
View the article (1.9 MB PDF)
Working with cultured dermal fibroblasts derived from control individuals and patients with systemic sclerosis (SSc), we have examined the effects of protein kinase C-delta (PKC-delta) on type I collagen biosynthesis and steady-state levels of COL1A1 and COL3A1 mRNAs. Rottlerin, a specific inhibitor of PKC-delta, exerted a powerful, dose-dependent inhibition of type I and type III collagen gene expression in normal and SSc cells. Optimal rottlerin concentrations caused a 70-90% inhibition of type I collagen production, a >80% reduction in COL1A1 mRNA, and a >70% reduction in COL3A1 mRNA in both cell types. In vitro nuclear transcription assays and transient transfections with COL1A1 promoter deletion constructs demonstrated that rottlerin profoundly reduced COL1A1 transcription and that this effect required a 129-bp promoter region encompassing nucleotides -804 to -675. This COL1A1 segment imparted rottlerin sensitivity to a heterologous promoter. Cotransfections of COL1A1 promoter constructs with a dominant-negative PKC-delta expression plasmid showed that suppression of this kinase silenced COL1A1 promoter activity. The results indicate that PKC-delta participates in the upregulation of collagen gene transcription in SSc and suggest that treatment with PKC-delta inhibitors could suppress fibrosis in this disease.