Literature DB >> 19443073

Growth arrest-specific protein 6 deficiency impairs liver tissue repair after acute toxic hepatitis in mice.

Fouad Lafdil1, Marie-Noële Chobert, Vanessa Deveaux, Elie-Serge Zafrani, Philippe Mavier, Toru Nakano, Yannick Laperche, Arthur Brouillet.   

Abstract

BACKGROUND/AIMS: Resident macrophages and myofibroblasts derived from hepatic stellate cells play a key role in liver wound healing. We previously reported that these sinusoidal cells secrete the growth arrest-specific protein 6 (Gas6) and express Axl, one of its receptors. Here we address the role of Gas6 in the healing process during acute liver injury.
METHODS: Toxic hepatitis was induced by a single carbon tetrachloride injection in Gas6 deficient (Gas6(-/-)) mice and liver recovery was compared with wild-type animals.
RESULTS: Gas6 deficiency did not cause any change in CCl(4)-induced liver damage. At 72 h, an efficient tissue repair was observed in wild-type animals whereas in Gas6(-/-) mice, we noticed a defective wound healing accounted by reduced Kupffer cell activation revealed by a decrease in the induction of CD14, TNF-alpha, IL6 and MCP-1. Gas6-deficiency, by limiting cytokine/chemokine release, prevents hepatocyte proliferation, recruitment of circulating monocytes and accumulation of myofibroblasts in healing areas. We also report a direct chemotactic effect of Gas6 on circulating monocytes which might explain defective macrophage infiltration in liver necrotic areas of Gas6(-/-) mice. Interestingly in Gas6(-/-) mice, we observed a high and constitutive expression of Axl and an induction of the suppressor of cytokine signaling SOCS1 after CCl(4) treatment.
CONCLUSIONS: The lower level of cytokines/chemokines in Gas6(-/-) mice after CCl(4) injury, is the consequence of an inhibitory signal arising from Axl receptor overexpression, leading to delayed liver repair in deficient mice.

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Year:  2009        PMID: 19443073     DOI: 10.1016/j.jhep.2009.02.030

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  18 in total

1.  Gas6/Axl pathway is activated in chronic liver disease and its targeting reduces fibrosis via hepatic stellate cell inactivation.

Authors:  Cristina Bárcena; Milica Stefanovic; Anna Tutusaus; Leonel Joannas; Anghara Menéndez; Carmen García-Ruiz; Pau Sancho-Bru; Montserrat Marí; Joan Caballeria; Carla V Rothlin; José C Fernández-Checa; Pablo García de Frutos; Albert Morales
Journal:  J Hepatol       Date:  2015-04-20       Impact factor: 25.083

2.  Liver precursor cells increase hepatic fibrosis induced by chronic carbon tetrachloride intoxication in rats.

Authors:  Marie-Noële Chobert; Dominique Couchie; Agnès Fourcot; Elie-Serge Zafrani; Yannick Laperche; Philippe Mavier; Arthur Brouillet
Journal:  Lab Invest       Date:  2011-09-26       Impact factor: 5.662

3.  Growth arrest-specific protein 6 is hepatoprotective against murine ischemia/reperfusion injury.

Authors:  Laura Llacuna; Cristina Bárcena; Lola Bellido-Martín; Laura Fernández; Milica Stefanovic; Montserrat Marí; Carmen García-Ruiz; José C Fernández-Checa; Pablo García de Frutos; Albert Morales
Journal:  Hepatology       Date:  2010-10       Impact factor: 17.425

4.  Autophagy induced by AXL receptor tyrosine kinase alleviates acute liver injury via inhibition of NLRP3 inflammasome activation in mice.

Authors:  Jihye Han; Joonbeom Bae; Chang-Yong Choi; Sang-Pil Choi; Hyung-Sik Kang; Eun-Kyeong Jo; Jongsun Park; Young Sik Lee; Hyun-Seuk Moon; Chung-Gyu Park; Myung-Shik Lee; Taehoon Chun
Journal:  Autophagy       Date:  2016-12       Impact factor: 16.016

5.  Growth arrest specific protein (GAS) 6: a role in the regulation of proliferation and functional capacity of the perinatal rat beta cell.

Authors:  T N Haase; M Rasmussen; C A M Jaksch; L W Gaarn; C K Petersen; N Billestrup; J H Nielsen
Journal:  Diabetologia       Date:  2013-01-19       Impact factor: 10.122

6.  T-Cell Immunoglobulin and Mucin Domain-Containing Protein-4 Is Critical for Kupffer Cell Homeostatic Function in the Activation and Resolution of Liver Ischemia Reperfusion Injury.

Authors:  Ming Ni; Jing Zhang; Rebecca Sosa; Hanwen Zhang; Han Wang; Dan Jin; Kaitlyn Crowley; Bita Naini; F Elaine Reed; Ronald W Busuttil; Jerzy W Kupiec-Weglinski; Xuehao Wang; Yuan Zhai
Journal:  Hepatology       Date:  2021-08-10       Impact factor: 17.298

Review 7.  Axl as a mediator of cellular growth and survival.

Authors:  Haley Axelrod; Kenneth J Pienta
Journal:  Oncotarget       Date:  2014-10-15

8.  Soluble Axl is an accurate biomarker of cirrhosis and hepatocellular carcinoma development: results from a large scale multicenter analysis.

Authors:  Mirko Dengler; Katharina Staufer; Heidemarie Huber; Rudolf Stauber; Heike Bantel; Karl Heinz Weiss; Patrick Starlinger; Hannelore Pock; Petra Klöters-Plachky; Daniel N Gotthardt; Peter Rauch; Carolin Lackner; Judith Stift; Christine Brostjan; Thomas Gruenberger; Takashi Kumada; Hidenori Toyoda; Toshifumi Tada; Thomas S Weiss; Michael Trauner; Wolfgang Mikulits
Journal:  Oncotarget       Date:  2017-07-11

9.  Effect of GAS6 and AXL Gene Polymorphisms on Adiposity, Systemic Inflammation, and Insulin Resistance in Adolescents.

Authors:  Fone-Ching Hsiao; Yuh-Feng Lin; Po-Shiuan Hsieh; Nain-Feng Chu; Yii-Der Ida Chen; Yi-Shing Shieh; Chang-Hsun Hsieh; Chien-Hsing Lee; Ting-I Lee; Yi-Jen Hung
Journal:  Int J Endocrinol       Date:  2014-02-18       Impact factor: 3.257

Review 10.  Candidate Biomarkers of Liver Fibrosis: A Concise, Pathophysiology-oriented Review.

Authors:  Mattia Bellan; Luigi Mario Castello; Mario Pirisi
Journal:  J Clin Transl Hepatol       Date:  2018-07-02
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