Lymphocytes contribute to biliary injury and fibrosis in experimental xenobiotic-induced cholestasis

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• 作者：Nikita Joshi^a ; ^b ; ^c ; Anna K. Kopec^b ; ^c ; Holly Cline-Fedewa^b ; James P. Luyendyk^a ; ^b ; ^c ; ^{luyendyk@cvm.msu.edu}
• 关键词：ANIT ; alpha-naphthylisothiocyanate ; CK-19 ; cytokeratin-19 ; ALT ; alanine aminotransferase ; ALP ; alkaline phosphatase ; TGFβ ; transforming growth factor beta ; COL1A1 ; type I collagen ; ITGβ6 ; integrin beta 6 ; αVβ6 ; alphaVbeta6 integrin ; PBC ; primary biliary cirrhosis ; PSC ; primary sclerosing cholangitis ; BDEC ; bile duct epithelial cell
• 刊名：Toxicology
• 出版年：2017
• 出版时间：15 February 2017
• 年：2017
• 卷：377
• 期：Complete
• 页码：73-80
• 全文大小：3672 K
• 卷排序：377

文摘

The etiology of chronic bile duct injury and fibrosis in patients with autoimmune cholestatic liver diseases is complex, and likely involves immune cells such as lymphocytes. However, most models of biliary fibrosis are not autoimmune in nature. Biliary fibrosis can be induced experimentally by prolonged exposure of mice to the bile duct toxicant alpha-naphthylisothiocyanate (ANIT). We determined whether lymphocytes contributed to ANIT-mediated biliary hyperplasia and fibrosis in mice. Hepatic accumulation of T-lymphocytes and increased serum levels of anti-nuclear-autoantibodies were evident in wild-type mice exposed to ANIT (0.05% ANIT in chow). This occurred alongside bile duct hyperplasia and biliary fibrosis. To assess the role of lymphocytes in ANIT-induced biliary fibrosis, we utilized RAG1−/− mice, which lack T- and B-lymphocytes. ANIT-induced bile duct injury, indicated by increased serum alkaline phosphatase activity, was reduced in ANIT-exposed RAG1−/− mice compared to ANIT-exposed wild-type mice. Despite this reduction in biliary injury, ANIT-induced bile duct hyperplasia was similar in wild-type and RAG1−/− mice. However, hepatic induction of profibrogenic genes including COL1A1, ITGβ6 and TGFβ2 was markedly attenuated in ANIT-exposed RAG1−/− mice compared to ANIT-exposed wild-type mice. Peribiliary collagen deposition was also reduced in ANIT-exposed RAG1−/− mice. The results indicate that lymphocytes exacerbate bile duct injury and fibrosis in ANIT-exposed mice without impacting bile duct hyperplasia.