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Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage

Liver fibrosis is a reversible wound-healing response to injury reflecting the critical balance between liver repair and scar formation. Chronic damage leads to progressive substitution of liver parenchyma by scar tissue and ultimately results in liver cirrhosis. Stromal cells (hepatic stellate cell...

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Autores principales: Mogler, Carolin, Wieland, Matthias, König, Courtney, Hu, Junhao, Runge, Anja, Korn, Claudia, Besemfelder, Eva, Breitkopf-Heinlein, Katja, Komljenovic, Dorde, Dooley, Steven, Schirmacher, Peter, Longerich, Thomas, Augustin, Hellmut G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364949/
https://www.ncbi.nlm.nih.gov/pubmed/25680861
http://dx.doi.org/10.15252/emmm.201404246
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author Mogler, Carolin
Wieland, Matthias
König, Courtney
Hu, Junhao
Runge, Anja
Korn, Claudia
Besemfelder, Eva
Breitkopf-Heinlein, Katja
Komljenovic, Dorde
Dooley, Steven
Schirmacher, Peter
Longerich, Thomas
Augustin, Hellmut G
author_facet Mogler, Carolin
Wieland, Matthias
König, Courtney
Hu, Junhao
Runge, Anja
Korn, Claudia
Besemfelder, Eva
Breitkopf-Heinlein, Katja
Komljenovic, Dorde
Dooley, Steven
Schirmacher, Peter
Longerich, Thomas
Augustin, Hellmut G
author_sort Mogler, Carolin
collection PubMed
description Liver fibrosis is a reversible wound-healing response to injury reflecting the critical balance between liver repair and scar formation. Chronic damage leads to progressive substitution of liver parenchyma by scar tissue and ultimately results in liver cirrhosis. Stromal cells (hepatic stellate cells [HSC] and endothelial cells) have been proposed to control the balance between liver fibrosis and regeneration. Here, we show that endosialin, a C-type lectin, expressed in the liver exclusively by HSC and portal fibroblasts, is upregulated in liver fibrosis in mouse and man. Chronic chemically induced liver damage resulted in reduced fibrosis and enhanced hepatocyte proliferation in endosialin-deficient (EN(KO)) mice. Correspondingly, acute-liver-damage-induced hepatocyte proliferation (partial hepatectomy) was increased in EN(KO) mice. A candidate-based screen of known regulators of hepatocyte proliferation identified insulin-like growth factor 2 (IGF2) as selectively endosialin-dependent hepatocyte mitogen. Collectively, the study establishes a critical role of HSC in the reciprocal regulation of fibrogenesis vs. hepatocyte proliferation and identifies endosialin as a therapeutic target in non-neoplastic settings.
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spelling pubmed-43649492015-03-23 Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage Mogler, Carolin Wieland, Matthias König, Courtney Hu, Junhao Runge, Anja Korn, Claudia Besemfelder, Eva Breitkopf-Heinlein, Katja Komljenovic, Dorde Dooley, Steven Schirmacher, Peter Longerich, Thomas Augustin, Hellmut G EMBO Mol Med Report Liver fibrosis is a reversible wound-healing response to injury reflecting the critical balance between liver repair and scar formation. Chronic damage leads to progressive substitution of liver parenchyma by scar tissue and ultimately results in liver cirrhosis. Stromal cells (hepatic stellate cells [HSC] and endothelial cells) have been proposed to control the balance between liver fibrosis and regeneration. Here, we show that endosialin, a C-type lectin, expressed in the liver exclusively by HSC and portal fibroblasts, is upregulated in liver fibrosis in mouse and man. Chronic chemically induced liver damage resulted in reduced fibrosis and enhanced hepatocyte proliferation in endosialin-deficient (EN(KO)) mice. Correspondingly, acute-liver-damage-induced hepatocyte proliferation (partial hepatectomy) was increased in EN(KO) mice. A candidate-based screen of known regulators of hepatocyte proliferation identified insulin-like growth factor 2 (IGF2) as selectively endosialin-dependent hepatocyte mitogen. Collectively, the study establishes a critical role of HSC in the reciprocal regulation of fibrogenesis vs. hepatocyte proliferation and identifies endosialin as a therapeutic target in non-neoplastic settings. BlackWell Publishing Ltd 2015-03 2015-02-13 /pmc/articles/PMC4364949/ /pubmed/25680861 http://dx.doi.org/10.15252/emmm.201404246 Text en © 2015 The Authors. Published under the terms of the CC BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Report
Mogler, Carolin
Wieland, Matthias
König, Courtney
Hu, Junhao
Runge, Anja
Korn, Claudia
Besemfelder, Eva
Breitkopf-Heinlein, Katja
Komljenovic, Dorde
Dooley, Steven
Schirmacher, Peter
Longerich, Thomas
Augustin, Hellmut G
Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage
title Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage
title_full Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage
title_fullStr Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage
title_full_unstemmed Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage
title_short Hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage
title_sort hepatic stellate cell-expressed endosialin balances fibrogenesis and hepatocyte proliferation during liver damage
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364949/
https://www.ncbi.nlm.nih.gov/pubmed/25680861
http://dx.doi.org/10.15252/emmm.201404246
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