The authors investigated the role of resveratrol (RV), a natural poliphenolic molecule with several biological activities,in transforming growth factor-β (TGF-β)–induced proliferation and differentiation of ex vivo human pulmonaryfibroblasts into myofibroblasts. The effects of RV treatment were evaluated by analyzing TGF-β–inducedα-smooth muscle actin (α-SMA) expression and collagen production, as well as cell proliferation of both normaland idiopathic pulmonary fibrosis (IPF) lung fibroblasts. Results demonstrate that RV inhibits TGF-β–inducedcell proliferation of both normal and pathological lung fibroblasts, attenuates α-SMA expression at both themRNA and protein levels, and also inhibits intracellular collagen deposition. In order to understand the molecularmechanisms, the authors also investigated the effects of RV treatment on signaling pathways involved inTGF-β–induced fibrosis. The authors show that RV inhibited TGF-β–induced phosphorylation of both extracellularsignal-regulated kinases (ERK1/2) and the serine/threonine kinase, Akt. Moreover, RV treatment blockedthe TGF-β–induced decrease in phosphatase and tensin homolog (PTEN) expression levels.

Resveratrol inhibits transforming growth factor-β-induced proliferation and differentiation of ex vivo human lung fibroblasts into myofibroblasts through ERK/Akt inhibition and PTEN restoration

FAGONE E;LO FURNO, DEBORA;GIUFFRIDA, Rosario;CRIMI, Nunzio;VANCHERI, CARLO
2011-01-01

Abstract

The authors investigated the role of resveratrol (RV), a natural poliphenolic molecule with several biological activities,in transforming growth factor-β (TGF-β)–induced proliferation and differentiation of ex vivo human pulmonaryfibroblasts into myofibroblasts. The effects of RV treatment were evaluated by analyzing TGF-β–inducedα-smooth muscle actin (α-SMA) expression and collagen production, as well as cell proliferation of both normaland idiopathic pulmonary fibrosis (IPF) lung fibroblasts. Results demonstrate that RV inhibits TGF-β–inducedcell proliferation of both normal and pathological lung fibroblasts, attenuates α-SMA expression at both themRNA and protein levels, and also inhibits intracellular collagen deposition. In order to understand the molecularmechanisms, the authors also investigated the effects of RV treatment on signaling pathways involved inTGF-β–induced fibrosis. The authors show that RV inhibited TGF-β–induced phosphorylation of both extracellularsignal-regulated kinases (ERK1/2) and the serine/threonine kinase, Akt. Moreover, RV treatment blockedthe TGF-β–induced decrease in phosphatase and tensin homolog (PTEN) expression levels.
2011
AKT; ERK1/2; human lung fibroblasts; IPF; myofibroblasts; PI3K; PTEN; resveratrol; TGF-β
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/20945
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