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Resumen de Expression of Matrix Metalloproteinases in Cyclosporin-Treated Gingival Fibroblasts Is Regulated by Transforming Growth Factor (TGF)-β1 Autocrine Stimulation

P. Cotrim, C.R. de Andrade, H. Martelli-Junior, E. Graner, John J. Sauk, Dr. R.D. Coletta

  • Background: Gingival overgrowth is a common side effect following the administration of cyclosporin A (CsA). The pathogenesis of this condition is not fully understood; however, recent studies show that CsA regulates the transcription of several cytokines including transforming growth factor-β1 (TGF-β1). The aim of this study was to investigate the potential role of TGF-β1 in the pathogenesis of CsA-induced gingival overgrowth, exploring a possible autocrine stimulation of TGF-β1 as a cellular regulator of synthesis of matrix metalloproteinases (MMPs) and its tissue inhibitors (TIMPs).

    Methods: Gingival fibroblasts from human normal gingiva were incubated with increasing concentrations of CsA, cultured for 24 hours, and the expression and production of TGF-β1 determined by semiquantitative reverse transcriptase-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA), respectively. MMP and TIMP mRNA expression levels were also analyzed by RT-PCR. To determine the effect of TGF-β1 on the expression of MMP and TIMP by human gingival fibroblasts under CsA treatment, human gingival fibroblast cultures were treated with sense oligonucleotides (SON) or antisense oligonucleotides (AON).

    Results: CsA simultaneously stimulated TGF-β1 expression and production and inhibited expression of MMP-1 and MMP-2 by human gingival fibroblasts, whereas CsA has a slight effect on TIMP-1 and TIMP-2 expression. AON reduced TGF-β1 production as demonstrated by ELISA, whereas TGF-β1 mRNA expression levels were not significantly modified. The inhibition of TGF-β1production byAONmodulated MMP expression, demonstrating the autocrine inhibitory effect of TGF-β1 in CsA-treated human gingival fibroblasts.

    Conclusions: The data presented here suggest that TGF-β1 in an autocrine fashion may contribute to a reduction of proteolytic activity of human gingival fibroblasts in CsA-induced gingival overgrowth, which favors the accumulation of extracellular matrix.


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