Hedgehog signaling regulates epithelial-mesenchymal transition during biliary fibrosis in rodents and humans
Alessia Omenetti, Alessandro Porrello, Youngmi Jung, Liu Yang, Yury Popov, Steve S. Choi, Rafal P. Witek, Gianfranco Alpini, Juliet Venter, Hendrika M. Vandongen, Wing-Kin Syn, Gianluca Svegliati Baroni, Antonio Benedetti, Detlef Schuppan, Anna Mae Diehl
Alessia Omenetti, Alessandro Porrello, Youngmi Jung, Liu Yang, Yury Popov, Steve S. Choi, Rafal P. Witek, Gianfranco Alpini, Juliet Venter, Hendrika M. Vandongen, Wing-Kin Syn, Gianluca Svegliati Baroni, Antonio Benedetti, Detlef Schuppan, Anna Mae Diehl
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Research Article

Hedgehog signaling regulates epithelial-mesenchymal transition during biliary fibrosis in rodents and humans

Abstract

Epithelial-mesenchymal transitions (EMTs) play an important role in tissue construction during embryogenesis, and evidence suggests that this process may also help to remodel some adult tissues after injury. Activation of the hedgehog (Hh) signaling pathway regulates EMT during development. This pathway is also induced by chronic biliary injury, a condition in which EMT has been suggested to have a role. We evaluated the hypothesis that Hh signaling promotes EMT in adult bile ductular cells (cholangiocytes). In liver sections from patients with chronic biliary injury and in primary cholangiocytes isolated from rats that had undergone bile duct ligation (BDL), an experimental model of biliary fibrosis, EMT was localized to cholangiocytes with Hh pathway activity. Relief of ductal obstruction in BDL rats reduced Hh pathway activity, EMT, and biliary fibrosis. In mouse cholangiocytes, coculture with myofibroblastic hepatic stellate cells, a source of soluble Hh ligands, promoted EMT and cell migration. Addition of Hh-neutralizing antibodies to cocultures blocked these effects. Finally, we found that EMT responses to BDL were enhanced in patched-deficient mice, which display excessive activation of the Hh pathway. Together, these data suggest that activation of Hh signaling promotes EMT and contributes to the evolution of biliary fibrosis during chronic cholestasis.

Authors

Alessia Omenetti, Alessandro Porrello, Youngmi Jung, Liu Yang, Yury Popov, Steve S. Choi, Rafal P. Witek, Gianfranco Alpini, Juliet Venter, Hendrika M. Vandongen, Wing-Kin Syn, Gianluca Svegliati Baroni, Antonio Benedetti, Detlef Schuppan, Anna Mae Diehl

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Figure 8

Myofibroblast-derived soluble factors increase motility/migration in cocultured cholangiocytes.

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Myofibroblast-derived soluble factors increase motility/migration in coc...
(A–F) Cell migration was assessed by wound-healing assay. Cholangiocytes were cultured in the absence (A and B) or presence (C–F) of Transwell filter inserts containing MF-HSCs for 6 days; cholangiocyte monolayers were then scratched, and an image was acquired immediately (time 0; A, C, and E) and 18 hours later after treatment with control IgG (B, D, and black bars) or Hh-neutralizing antibody (NAb) (F and gray bars). Cholangiocyte migration was quantified by measuring the distance dividing the 2 sides of the monolayer using Image J software (G) and by counting the numbers of cells that had migrated into the wound after 18 hours (H). **P < 0.005 versus monocultures, time 0 (G) or IgG-treated monoculture (H); #P < 0.005 versus IgG-treated coculture. Original magnification, ×10 (A–F). The dashed lines (A–F) indicate the leading edge of the cut that was made across the monolayers.