Gliotoxin stimulates the apoptosis of human and rat hepatic stellate cells and enhances the resolution of liver fibrosis in rats


Wright, Matthew C., Issa, Razo, Smart, David E., Trim, Nathan, Murray, Graeme I., Primrose, John N., Arthur, Michael J.P., Iredale, John P. and Mann, Derek A. (2001) Gliotoxin stimulates the apoptosis of human and rat hepatic stellate cells and enhances the resolution of liver fibrosis in rats. Gastroenterology, 121, (3), 685-698. (doi:10.1053/gast.2001.27188).

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Original Publication URL: http://dx.doi.org/10.1053/gast.2001.27188

Description/Abstract

Background & Aims: Hepatic stellate cells (HSCs) play a pivotal role in liver fibrosis and stimulating their apoptosis could be an effective treatment for liver fibrosis.

Methods: Activated HSCs, hepatocytes, and rats with liver fibrosis were treated with gliotoxin.

Results: Addition of gliotoxin to activated (-smooth muscle actin positive) rat and human HSCs resulted in morphologic alterations typical of apoptosis. Within 2–3 hours of incubation, caspase 3 activity was markedly induced and caspase inhibitor 1 (Z-VAD-FMK)-sensitive oligonucleosome-length DNA fragments were detectable by gel electrophoresis of low molecular weight DNA. Apoptosis was widespread as judged by fluorescence-activated cell sorter analysis and terminal deoxynucleotidyl transferase–mediated deoxyuridine triphosphate nick-end labeling staining in both rat and human HSCs at concentrations that had no effect on the viability of rat hepatocytes. Gliotoxin treatment significantly reduced the number of activated stellate cells and mean thickness of bridging fibrotic septae in livers from rats treated with carbon tetrachloride.

Conclusions: These data demonstrate proof-of-concept that by up-regulating HSC apoptosis, the extent of fibrosis can be decreased in inflammatory liver injury.

Item Type: Article
ISSNs: 0016-5085 (print)
Related URLs:
Subjects: R Medicine > RB Pathology
Divisions: University Structure - Pre August 2011 > School of Medicine > Cancer Sciences
University Structure - Pre August 2011 > School of Medicine > Infection, Inflammation and Repair
ePrint ID: 26671
Date Deposited: 24 Apr 2006
Last Modified: 27 Mar 2014 18:15
Contact Email Address: J.P.Iredale@soton.ac.uk
URI: http://eprints.soton.ac.uk/id/eprint/26671

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