Lysyl oxidase-like protein 2 (LOXL2) modulates barrier function in cholangiocytes in cholestasis
| Autor: | Silvia Racedo, Christopher L. Bowlus, Derek Marshall, Hans Jürgen Gruber, Carolin Lackner, Emmanuel Moreau, Johannes R. Hov, Marion J. Pollheimer, Tor J. Eide, Joanne I. Adamkewicz, Victoria Smith, Amanda Mikels-Vigdal, Tobias Madl, Tom H. Karlsen, Rudolf E. Stauber, Hubert Scharnagl, Peter Fickert, Tatjana Stojakovic, Gernot Zollner, Michael Trauner, Susan K. Lyman |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Biliary Tract Diseases Primary sclerosing cholangitis 03 medical and health sciences chemistry.chemical_compound Mice Downregulation and upregulation Cholestasis Fibrosis Chenodeoxycholic acid medicine Animals Biliary Tract Barrier function Cells Cultured Cellular Senescence Cell Proliferation Hepatology LOXL2 Bile duct Epithelial Cells medicine.disease Cadherins Disease Models Animal 030104 developmental biology medicine.anatomical_structure chemistry Cancer research Amino Acid Oxidoreductases |
| Zdroj: | Journal of hepatology. 69(2) |
| ISSN: | 1600-0641 |
| Popis: | Background & Aims The lysyl oxidase-like protein 2 (LOXL2) promotes stabilization of the extracellular matrix, chemotaxis, cell growth and cell mobility. We aimed to (i) identify stimuli of LOXL2 in cholangiopathies, (ii) characterize the effects of LOXL2 on biliary epithelial cells’ (BECs) barrier function, (iii) compare LOXL2 expression in primary sclerosing cholangitis (PSC), primary biliary cholangitis, and disease controls, and (iv) to determine LOXL2 expression and its cellular sources in four mouse models of cholangiopathies. Methods Cultured murine BECs were challenged with well-known triggers of cellular senescence, hypoxia, phospholipid-deficient Abcb4−/− mouse bile and chenodeoxycholic acid and investigated for LOXL2, SNAIL1 and E-cadherin expression and transepithelial electrical resistance with and without LOX-inhibition. In vivo, LOXL2 expression was studied in PSC livers, and controls and mouse models. We compared LOXL2 serum levels in patients with PSC, secondary SC, primary biliary cholangitis, and controls. Results Cellular senescence, hypoxia, Abcb4−/− bile and chenodeoxycholic acid induced LOXL2 and SNAIL1 expression, repressed E-cadherin expression, and significantly reduced transepithelial electrical resistance in BECs. Notably, all of the pathological changes could be recovered via pharmacological LOX-inhibition. Mouse models showed induced LOXL2 expression in the portal region and in association with ductular reaction. LOXL2 serum levels were significantly elevated in patients with cholangiopathies. In PSC, LOXL2 expression was located to characteristic periductal onion skin-type fibrosis, ductular reaction, Kupffer cells, and fibrotic septa. Importantly, in PSC, LOXL2 overexpression was paralleled by E-cadherin loss in BECs from medium-sized bile ducts. Conclusions Reactive BECs produce LOXL2, resulting in increased tight junction permeability, which can be ameliorated by pharmacological LOX-inhibition in vitro. Reactive BECs, portal myofibroblasts, and Kupffer cells are the main sources of LOXL2 in cholangiopathies. Lay summary In this study, we investigate the role of lysyl oxidase-like protein 2 (LOXL2), an enzyme pivotal in the development of organ fibrosis, in the pathogenesis of cholangiopathies (diseases of bile ducts), such as primary sclerosing cholangitis. We found LOXL2 to be expressed in association with bile duct epithelial injury and uncovered mechanisms for its upregulation and the subsequent effects in vitro and in vivo. Our findings support testing of anti-LOXL2 treatment strategies for patients with primary sclerosing cholangitis. |
| Databáze: | OpenAIRE |
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