Literature DB >> 24619965

Angiotensin-II type 1 receptor-mediated Janus kinase 2 activation induces liver fibrosis.

Michaela Granzow1, Robert Schierwagen, Sabine Klein, Benita Kowallick, Sebastian Huss, Markus Linhart, Irela G Reza Mazar, Jan Görtzen, Annabelle Vogt, Frank A Schildberg, Maria A Gonzalez-Carmona, Alexandra Wojtalla, Benjamin Krämer, Jacob Nattermann, Sören V Siegmund, Nikos Werner, Dieter O Fürst, Wim Laleman, Percy Knolle, Vijay H Shah, Tilman Sauerbruch, Jonel Trebicka.   

Abstract

UNLABELLED: Activation of the renin angiotensin system resulting in stimulation of angiotensin-II (AngII) type I receptor (AT1R) is an important factor in the development of liver fibrosis. Here, we investigated the role of Janus kinase 2 (JAK2) as a newly described intracellular effector of AT1R in mediating liver fibrosis. Fibrotic liver samples from rodents and humans were compared to respective controls. Transcription, protein expression, activation, and localization of JAK2 and downstream effectors were analyzed by real-time polymerase chain reaction, western blotting, immunohistochemistry, and confocal microscopy. Experimental fibrosis was induced by bile duct ligation (BDL), CCl4 intoxication, thioacetamide intoxication or continuous AngII infusion. JAK2 was inhibited by AG490. In vitro experiments were performed with primary rodent hepatic stellate cells (HSCs), Kupffer cells (KCs), and hepatocytes as well as primary human and human-derived LX2 cells. JAK2 expression and activity were increased in experimental rodent and human liver fibrosis, specifically in myofibroblastic HSCs. AT1R stimulation in wild-type animals led to activation of HSCs and fibrosis in vivo through phosphorylation of JAK2 and subsequent RhoA/Rho-kinase activation. These effects were prevented in AT1R(-/-) mice. Pharmacological inhibition of JAK2 attenuated liver fibrosis in rodent fibrosis models. In vitro, JAK2 and downstream effectors showed increased expression and activation in activated HSCs, when compared to quiescent HSCs, KCs, and hepatocytes isolated from rodents. In primary human and LX2 cells, AG490 blocked AngII-induced profibrotic gene expression. Overexpression of JAK2 led to increased profibrotic gene expression in LX2 cells, which was blocked by AG490.
CONCLUSION: Our study substantiates the important cell-intrinsic role of JAK2 in HSCs for development of liver fibrosis. Inhibition of JAK2 might therefore offer a promising therapy for liver fibrosis.
© 2014 by the American Association for the Study of Liver Diseases.

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Year:  2014        PMID: 24619965      PMCID: PMC5512562          DOI: 10.1002/hep.27117

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  46 in total

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2.  HSC-specific inhibition of Rho-kinase reduces portal pressure in cirrhotic rats without major systemic effects.

Authors:  Sabine Klein; Marike Marjolijn Van Beuge; Michaela Granzow; Leonie Beljaars; Robert Schierwagen; Sibel Kilic; Iren Heidari; Sebastian Huss; Tilman Sauerbruch; Klaas Poelstra; Jonel Trebicka
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6.  Atorvastatin attenuates angiotensin II-induced inflammatory actions in the liver.

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8.  Hemodynamic and antifibrotic effects of losartan in rats with liver fibrosis and/or portal hypertension.

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Review 10.  Modern pathogenetic concepts of liver fibrosis suggest stellate cells and TGF-beta as major players and therapeutic targets.

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Journal:  J Cell Mol Med       Date:  2006 Jan-Mar       Impact factor: 5.310

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  55 in total

1.  Magnesium isoglycyrrhizinate ameliorates high fructose-induced liver fibrosis in rat by increasing miR-375-3p to suppress JAK2/STAT3 pathway and TGF-β1/Smad signaling.

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Review 3.  Novelties in the pathophysiology and management of portal hypertension: new treatments on the horizon.

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Journal:  Hepatol Int       Date:  2017-07-11       Impact factor: 6.047

4.  Targeting the renin-angiotensin-aldosterone system in fibrosis.

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Review 5.  Pathobiology of liver fibrosis: a translational success story.

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6.  Short-term administration of GW501516 improves inflammatory state in white adipose tissue and liver damage in high-fructose-fed mice through modulation of the renin-angiotensin system.

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Review 7.  Mechanisms of hepatic stellate cell activation.

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8.  Hepatic stellate cell activation and pro-fibrogenic signals.

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9.  Synectin promotes fibrogenesis by regulating PDGFR isoforms through distinct mechanisms.

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Review 10.  Antifibrotics in liver disease: are we getting closer to clinical use?

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Journal:  Hepatol Int       Date:  2018-10-09       Impact factor: 6.047

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