Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver Fibrosis
Abstract Liver fibrosis is the most serious pathology caused by Schistosoma japonicum infection, which arises when schistosome eggs are deposited in the liver. Eosinophils, macrophages and hepatic stellate cells (HSCs) have been identified as major cellular contributors to the development of granulo...
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doaj-7dd38bfeefb5460cab250026cddcef852020-12-08T02:49:56ZengNature Publishing GroupScientific Reports2045-23222017-03-017111410.1038/s41598-017-00377-4Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver FibrosisQi Wang0Xin Chou1Fei Guan2Zhengming Fang3Shengjun Lu4Jiahui Lei5Yonglong Li6Wenqi Liu7Department of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Parasitology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and TechnologyAbstract Liver fibrosis is the most serious pathology caused by Schistosoma japonicum infection, which arises when schistosome eggs are deposited in the liver. Eosinophils, macrophages and hepatic stellate cells (HSCs) have been identified as major cellular contributors to the development of granulomas and fibrosis, but little is known about the effects of hepatocytes on granuloma formation. Here, we found that the levels of Wnt signalling-related molecules, transforming growth factor β (TGF-β) and connective tissue growth factor (CTGF) in hepatocytes were markedly elevated after S. japonicum infection. Liver fibrosis was exacerbated when exogenous Wnt3a was introduced, but was alleviated when Wnt signalling was suppressed by DKK1, accompanied by the reduced expression of TGF-β and CTGF in hepatocytes. These results indicate that the hepatocytic expression of TGF-β and CTGF is mediated by Wnt signalling. Additionally, the hepatocytes isolated from infected mice promoted the activation of primary HSCs in vitro, however, this effect was not observed when hepatocytes from DKK1 treated S. japonicum-infected mice was employed in the co-culture system. Our findings identify a novel pro-fibrogenic role of hepatocytes in schistosomiasis-induced liver fibrosis that is dependent on Wnt signalling, which may serve as a potential target for ameliorating hepatic fibrosis caused by helminths.https://doi.org/10.1038/s41598-017-00377-4 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Qi Wang Xin Chou Fei Guan Zhengming Fang Shengjun Lu Jiahui Lei Yonglong Li Wenqi Liu |
spellingShingle |
Qi Wang Xin Chou Fei Guan Zhengming Fang Shengjun Lu Jiahui Lei Yonglong Li Wenqi Liu Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver Fibrosis Scientific Reports |
author_facet |
Qi Wang Xin Chou Fei Guan Zhengming Fang Shengjun Lu Jiahui Lei Yonglong Li Wenqi Liu |
author_sort |
Qi Wang |
title |
Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver Fibrosis |
title_short |
Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver Fibrosis |
title_full |
Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver Fibrosis |
title_fullStr |
Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver Fibrosis |
title_full_unstemmed |
Enhanced Wnt Signalling in Hepatocytes is Associated with Schistosoma japonicum Infection and Contributes to Liver Fibrosis |
title_sort |
enhanced wnt signalling in hepatocytes is associated with schistosoma japonicum infection and contributes to liver fibrosis |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-03-01 |
description |
Abstract Liver fibrosis is the most serious pathology caused by Schistosoma japonicum infection, which arises when schistosome eggs are deposited in the liver. Eosinophils, macrophages and hepatic stellate cells (HSCs) have been identified as major cellular contributors to the development of granulomas and fibrosis, but little is known about the effects of hepatocytes on granuloma formation. Here, we found that the levels of Wnt signalling-related molecules, transforming growth factor β (TGF-β) and connective tissue growth factor (CTGF) in hepatocytes were markedly elevated after S. japonicum infection. Liver fibrosis was exacerbated when exogenous Wnt3a was introduced, but was alleviated when Wnt signalling was suppressed by DKK1, accompanied by the reduced expression of TGF-β and CTGF in hepatocytes. These results indicate that the hepatocytic expression of TGF-β and CTGF is mediated by Wnt signalling. Additionally, the hepatocytes isolated from infected mice promoted the activation of primary HSCs in vitro, however, this effect was not observed when hepatocytes from DKK1 treated S. japonicum-infected mice was employed in the co-culture system. Our findings identify a novel pro-fibrogenic role of hepatocytes in schistosomiasis-induced liver fibrosis that is dependent on Wnt signalling, which may serve as a potential target for ameliorating hepatic fibrosis caused by helminths. |
url |
https://doi.org/10.1038/s41598-017-00377-4 |
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