A synthetic PPAR-γ agonist triterpenoid ameliorates experimental fibrosis: PPAR-γ-independent suppression of fibrotic responses

作者：Wei, Jun; Zhu, Hongyan; Komura, Kazuhiro; Lord, Gabriel; Tomcik, Michal; Wang, Wenxia; Doniparthi, Sruthi; Tamaki, Zenshiro; Hinchcliff, Monique; Distler, Joerg H. W.; Varga, John^*

来源：Annals of the Rheumatic Diseases, 2014, 73(2): 446-454.

DOI：10.1136/annrheumdis-2012-202716

• ACTIVATED RECEPTOR-GAMMA
• GROWTH-FACTOR-BETA
• STELLATE CELL ACTIVATION
• TGF-BETA
• SYSTEMIC-SCLEROSIS
• SKIN FIBROBLASTS
• IN-VITRO
• MYOFIBROBLAST DIFFERENTIATION
• PROFIBROTIC RESPONSES
• MYOCARDIAL-INFARCTION

Background Persistent fibroblast activation initiated by transforming growth factor beta (TGF-beta) is a fundamental event in the pathogenesis of systemic sclerosis, and its pharmacological inhibition represents a potential therapeutic strategy. The nuclear receptor, peroxisome proliferator-activated receptor. (PPAR-gamma), exerts potent fibrotic activity. The synthetic oleanane triterpenoid, 2-cyano-3,12-dioxo-olean-1,9-dien-28-oic acid (CDDO), is a PPAR-gamma agonist with potential effects on TGF-beta signalling and dermal fibrosis. @@@ Objective To examine the modulation of fibrogenesis by CDDO in explanted fibroblasts, skin organ cultures and murine models of scleroderma. @@@ Material and methods The effects of CDDO on experimental fibrosis induced by bleomycin injection or by overexpression of constitutively active type I TGF-beta receptor (TgfbR1ca) were evaluated. Modulation of fibrotic gene expression was examined in human skin organ cultures. To delineate the mechanisms underlying the antifibrotic effects of CDDO, explanted skin fibroblasts cultured in two-dimensional monolayers or in three-dimensional full-thickness human skin equivalents were studied. @@@ Results CDDO significantly ameliorated dermal fibrosis in two complementary mouse models of scleroderma, as well as in human skin organ cultures and in three-dimensional human skin equivalents. In two-dimensional monolayer cultures of explanted normal fibroblasts, CDDO abrogated fibrogenic responses induced by TGF-beta. These CDDO effects occurred via disruption of Smad-dependent transcription and were associated with inhibition of Akt activation. In scleroderma fibroblasts, CDDO attenuated the elevated synthesis of collagen. Remarkably, the in vitro antifibrotic effects of CDDO were independent of PPAR-gamma. @@@ Conclusions The PPAR-gamma agonist triterpenoid CDDO attenuates fibrogenesis by antagonistically targeting canonical TGF-beta/Smad and Akt signalling in a PPAR-gamma-independent manner. These findings identify this synthetic triterpenoid as a potential new therapy for the control of fibrosis.

• 出版日期2014-2
• 单位西北大学