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- W2124503885 abstract "Abstract: Background/Aims: Collagen production by activated hepatic stellate cells (HSCs) is a key event in liver fibrosis, and a number of factors have been characterized that trigger HSC activation and collagen production. However, it remains unclear if these factors act locally at the site of injury or also affect HSCs distant to the site of injury. Methods: A model of partial bile duct ligation (PBDL) in which fibrogenesis can be compared between the injured ligated lobe and the non‐ligated lobe. Results: After PBDL, HSCs showed an increased expression of procollagen type I α1 mRNA and collagen‐reporter gene activity not only in the ligated lobe, but also in the non‐ligated lobe, albeit at a lower level. In contrast, an increase in the number of desmin‐ and α‐smooth muscle actin positive HSCs, and accumulation of inflammatory cells were observed only in the ligated lobe. Although transforming growth factor‐β (TGF‐β) mRNA was increased only in the ligated lobe, Smad2/3 were activated in the ligated and the non‐ligated lobe. These data suggest that the systemic increase in profibrogenic mediators including TGF‐β induces collagen transcription in the uninjured liver. Conclusion: Systemic profibrogenic mediators from the injury site affect the residual non‐injured liver." @default.
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- W2124503885 date "2006-10-10" @default.
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- W2124503885 title "Systemic mediators induce fibrogenic effects in normal liver after partial bile duct ligation" @default.
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- W2124503885 doi "https://doi.org/10.1111/j.1478-3231.2006.01346.x" @default.
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