Secreted frizzled related proteins inhibit fibrosis in vitro but appear redundant in vivo
The pathogenesis of pulmonary fibrosis remains poorly understood. The Wnt signaling pathway regulates fibrogenesis in different organs. Here, we studied the role of two extracellular Wnt antagonists, secreted frizzled-related protein-1 (SFRP1) and frizzled-related protein (FRZB) on lung fibrosis in...
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Veröffentlicht in: | Fibrogenesis & Tissue Repair 2014-10, Vol.7 (1), p.1-10 |
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creator | De Langhe, Ellen Aznar Lopez, Carolina De Vooght, Vanessa Vanoirbeek, Jeroen Luyten, Frank Lories, Rik |
description | The pathogenesis of pulmonary fibrosis remains poorly understood. The Wnt signaling pathway regulates fibrogenesis in different organs. Here, we studied the role of two extracellular Wnt antagonists, secreted frizzled-related protein-1 (SFRP1) and frizzled-related protein (FRZB) on lung fibrosis in vitro and in vivo. For this purpose, we used an alveolar epithelial cell line and a lung fibroblast cell line, and the bleomycin-induced lung fibrosis model, respectively. |
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The Wnt signaling pathway regulates fibrogenesis in different organs. Here, we studied the role of two extracellular Wnt antagonists, secreted frizzled-related protein-1 (SFRP1) and frizzled-related protein (FRZB) on lung fibrosis in vitro and in vivo. For this purpose, we used an alveolar epithelial cell line and a lung fibroblast cell line, and the bleomycin-induced lung fibrosis model, respectively.</abstract><pub>BioMed Central</pub><oa>free_for_read</oa></addata></record> |
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title | Secreted frizzled related proteins inhibit fibrosis in vitro but appear redundant in vivo |
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