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E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis

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 t...

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Autores principales: Hasegawa, Daisuke, Fujii, Ryoji, Yagishita, Naoko, Matsumoto, Nobuyuki, Aratani, Satoko, Izumi, Toshihiko, Azakami, Kazuko, Nakazawa, Minako, Fujita, Hidetoshi, Sato, Tomoo, Araya, Natsumi, Koike, Junki, Tadokoro, Mamoru, Suzuki, Noboru, Nagata, Kazuhiro, Senoo, Haruki, Friedman, Scott L., Nishioka, Kusuki, Yamano, Yoshihisa, Itoh, Fumio, Nakajima, Toshihiro
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2963597/
https://www.ncbi.nlm.nih.gov/pubmed/21049091
http://dx.doi.org/10.1371/journal.pone.0013590
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author Hasegawa, Daisuke
Fujii, Ryoji
Yagishita, Naoko
Matsumoto, Nobuyuki
Aratani, Satoko
Izumi, Toshihiko
Azakami, Kazuko
Nakazawa, Minako
Fujita, Hidetoshi
Sato, Tomoo
Araya, Natsumi
Koike, Junki
Tadokoro, Mamoru
Suzuki, Noboru
Nagata, Kazuhiro
Senoo, Haruki
Friedman, Scott L.
Nishioka, Kusuki
Yamano, Yoshihisa
Itoh, Fumio
Nakajima, Toshihiro
author_facet Hasegawa, Daisuke
Fujii, Ryoji
Yagishita, Naoko
Matsumoto, Nobuyuki
Aratani, Satoko
Izumi, Toshihiko
Azakami, Kazuko
Nakazawa, Minako
Fujita, Hidetoshi
Sato, Tomoo
Araya, Natsumi
Koike, Junki
Tadokoro, Mamoru
Suzuki, Noboru
Nagata, Kazuhiro
Senoo, Haruki
Friedman, Scott L.
Nishioka, Kusuki
Yamano, Yoshihisa
Itoh, Fumio
Nakajima, Toshihiro
author_sort Hasegawa, Daisuke
collection PubMed
description 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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spelling pubmed-29635972010-11-03 E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis Hasegawa, Daisuke Fujii, Ryoji Yagishita, Naoko Matsumoto, Nobuyuki Aratani, Satoko Izumi, Toshihiko Azakami, Kazuko Nakazawa, Minako Fujita, Hidetoshi Sato, Tomoo Araya, Natsumi Koike, Junki Tadokoro, Mamoru Suzuki, Noboru Nagata, Kazuhiro Senoo, Haruki Friedman, Scott L. Nishioka, Kusuki Yamano, Yoshihisa Itoh, Fumio Nakajima, Toshihiro PLoS One Research Article 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. Public Library of Science 2010-10-25 /pmc/articles/PMC2963597/ /pubmed/21049091 http://dx.doi.org/10.1371/journal.pone.0013590 Text en Hasegawa et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hasegawa, Daisuke
Fujii, Ryoji
Yagishita, Naoko
Matsumoto, Nobuyuki
Aratani, Satoko
Izumi, Toshihiko
Azakami, Kazuko
Nakazawa, Minako
Fujita, Hidetoshi
Sato, Tomoo
Araya, Natsumi
Koike, Junki
Tadokoro, Mamoru
Suzuki, Noboru
Nagata, Kazuhiro
Senoo, Haruki
Friedman, Scott L.
Nishioka, Kusuki
Yamano, Yoshihisa
Itoh, Fumio
Nakajima, Toshihiro
E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis
title E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis
title_full E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis
title_fullStr E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis
title_full_unstemmed E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis
title_short E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis
title_sort e3 ubiquitin ligase synoviolin is involved in liver fibrogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2963597/
https://www.ncbi.nlm.nih.gov/pubmed/21049091
http://dx.doi.org/10.1371/journal.pone.0013590
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