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E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis

Daisuke HasegawaInstitute of Medical Science, St Marianna University School of Medicine, Kawasaki, JapanRyoji FujiiInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanNaoko YagishitaInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanNobuyuki MatsumotoDivision of Gastroenterology and Hepatology, St. Marianna University School of Medicine, Kawasaki, JapanSatoko ArataniInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanToshihiko IzumiInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanKazuko AzakamiInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanMinako NakazawaInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanHidetoshi FujitaInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanTomoo SatoInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanNatsumi ArayaInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanJunki KoikeDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, JapanMamoru TadokoroDepartment of Pathology, St. Marianna University School of Medicine, Kawasaki, JapanNoboru SuzukiDepartments of Immunology and Medicine, St. Marianna University School of Medicine, Kawasaki, JapanKazuhiro NagataDepartment of Molecular and Cellular Biology, Institute for Frontier Medical Sciences, Kyoto University, Kyoto, JapanHaruki SenooDepartment of Cell Biology and Histology, Akita University School of Medicine, Hondo, JapanScott L. FriedmanDivision of Liver Diseases, Mount Sinai School of Medicine, New York, New York, United States of AmericaKusuki NishiokaInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanYoshihisa YamanoInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki, JapanFumio ItohDivision of Gastroenterology and Hepatology, St. Marianna University School of Medicine, Kawasaki, JapanToshihiro NakajimaChoju Medical Institute Fukushimura Hospital, Toyohasi, Japan
2010en
ABI

Аннотация

BACKGROUND AND AIM: Chronic hepatic damage leads to liver fibrosis, which is characterized by the accumulation of collagen-rich extracellular matrix. However, the mechanism by which E3 ubiquitin ligase is involved in collagen synthesis in liver fibrosis is incompletely understood. This study aimed to explore the involvement of the E3 ubiquitin ligase synoviolin (Syno) in liver fibrosis. METHODS: The expression and localization of synoviolin in the liver were analyzed in CCl(4)-induced hepatic injury models and human cirrhosis tissues. The degree of liver fibrosis and the number of activated hepatic stellate cells (HSCs) was compared between wild type (wt) and Syno(+/-) mice in the chronic hepatic injury model. We compared the ratio of apoptosis in activated HSCs between wt and Syno(+/-) mice. We also analyzed the effect of synoviolin on collagen synthesis in the cell line from HSCs (LX-2) using siRNA-synoviolin and a mutant synoviolin in which E3 ligase activity was abolished. Furthermore, we compared collagen synthesis between wt and Syno(-/-) mice embryonic fibroblasts (MEF) using quantitative RT-PCR, western blotting, and collagen assay; then, we immunohistochemically analyzed the localization of collagen in Syno(-/-) MEF cells. RESULTS: In the hepatic injury model as well as in cirrhosis, synoviolin was upregulated in the activated HSCs, while Syno(+/-) mice developed significantly less liver fibrosis than in wt mice. The number of activated HSCs was decreased in Syno(+/-) mice, and some of these cells showed apoptosis. Furthermore, collagen expression in LX-2 cells was upregulated by synoviolin overexpression, while synoviolin knockdown led to reduced collagen expression. Moreover, in Syno(-/-) MEF cells, the amounts of intracellular and secreted mature collagen were significantly decreased, and procollagen was abnormally accumulated in the endoplasmic reticulum. CONCLUSION: Our findings demonstrate the importance of the E3 ubiquitin ligase synoviolin in liver fibrosis.

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