Activation of canonical Wnt signalling is required for TGF-β-mediated fibrosis

被引:685
作者
Akhmetshina, Alfiya [1 ,2 ]
Palumbo, Katrin [1 ,2 ]
Dees, Clara [1 ,2 ]
Bergmann, Christina [1 ,2 ]
Venalis, Paulius [1 ,2 ]
Zerr, Pawel [1 ,2 ]
Horn, Angelika [1 ,2 ]
Kireva, Trayana [1 ,2 ]
Beyer, Christian [1 ,2 ]
Zwerina, Jochen [1 ,2 ]
Schneider, Holm [3 ]
Sadowski, Anika [3 ]
Riener, Marc-Oliver [4 ]
MacDougald, Ormond A. [5 ]
Distler, Oliver [6 ,7 ]
Schett, Georg [1 ,2 ]
Distler, Joerg H. W. [1 ,2 ]
机构
[1] Univ Erlangen Nurnberg, Dept Internal Med 3, D-91054 Erlangen, Germany
[2] Univ Erlangen Nurnberg, Inst Clin Immunol, D-91054 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Dept Pediat, D-91054 Erlangen, Germany
[4] Univ Erlangen Nurnberg, Dept Pathol, D-91054 Erlangen, Germany
[5] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48105 USA
[6] Univ Zurich Hosp, Ctr Expt Rheumatol, CH-8091 Zurich, Switzerland
[7] Univ Zurich Hosp, Zurich Ctr Integrat Human Physiol, CH-8091 Zurich, Switzerland
关键词
GROWTH-FACTOR-BETA; SYSTEMIC-SCLEROSIS; EXTRACELLULAR-MATRIX; MECHANISMS; DICKKOPF-1; PATHWAY; FIBROBLASTS; INHIBITION; EXPRESSION; PROTEINS;
D O I
10.1038/ncomms1734
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The transforming growth factor-beta (TGF-beta) signalling pathway is a key mediator of fibroblast activation that drives the aberrant synthesis of extracellular matrix in fibrotic diseases. Here we demonstrate a novel link between transforming growth factor-beta and the canonical Wnt pathway. TGF-beta stimulates canonical Wnt signalling in a p38-dependent manner by decreasing the expression of the Wnt antagonist Dickkopf-1. Tissue samples from human fibrotic diseases show enhanced expression of Wnt proteins and decreased expression of Dickkopf-1. Activation of the canonical Wnt pathway stimulates fibroblasts in vitro and induces fibrosis in vivo. Transgenic overexpression of Dickkopf-1 ameliorates skin fibrosis induced by constitutively active TGF-beta receptor type I signalling and also prevents fibrosis in other TGF-beta-dependent animal models. These findings demonstrate that canonical Wnt signalling is necessary for TGF-beta-mediated fibrosis and highlight a key role for the interaction of both pathways in the pathogenesis of fibrotic diseases.
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页数:12
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