Hepatocyte growth factor in dampening liver immune‐mediated pathology in acute viral hepatitis without compromising antiviral activity. Issue 4 (April 2014)
- Record Type:
- Journal Article
- Title:
- Hepatocyte growth factor in dampening liver immune‐mediated pathology in acute viral hepatitis without compromising antiviral activity. Issue 4 (April 2014)
- Main Title:
- Hepatocyte growth factor in dampening liver immune‐mediated pathology in acute viral hepatitis without compromising antiviral activity
- Authors:
- Aguilar‐Valenzuela, Renan
Carlsen, Eric D.
Liang, Yuejin
Soong, Lynn
Sun, Jiaren - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12456-sec-0001" sec-type="section"> <title>Background and Aim</title> <p>Hepatocyte growth factor (HGF) is a pleiotropic cytokine related with cell proliferation and survival; however, its role in viral hepatitis is not elucidated. In this study, we studied HGF immune role in viral hepatitis.</p> </sec> <sec id="jgh12456-sec-0002" sec-type="section"> <title>Methods</title> <p>Mice received hydrodynamically delivered HGF plasmid or control plasmid and then infected with adenovirus, and parameters of immune‐mediated liver damage were evaluated. We studied dendritic cell (DC) activation in the presence of HGF. T cells collected from infected mice were restimulated with virally infected DC to measure cytokine production <italic>in vitro</italic>.</p> </sec> <sec id="jgh12456-sec-0003" sec-type="section"> <title>Results</title> <p>HGF ameliorated the liver inflammation during viral hepatitis as alanine transferase, intrahepatic lymphocytes, and splenocyte counts were diminished by HGF. Lower histological scores of liver pathology were observed in the HGF group. DC from the HGF group expressed reduced CD40. The hepatic expression and serum concentration of IL‐12p40 were diminished in HGF‐transfected mice. <italic>In vitro</italic> experiments with DC confirmed that HGF diminished CD40 expression and IL‐12p40 production. The expression and serum levels of IFN‐γ, IL‐6 and CXCL9 were significantly decreased in the<abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12456-sec-0001" sec-type="section"> <title>Background and Aim</title> <p>Hepatocyte growth factor (HGF) is a pleiotropic cytokine related with cell proliferation and survival; however, its role in viral hepatitis is not elucidated. In this study, we studied HGF immune role in viral hepatitis.</p> </sec> <sec id="jgh12456-sec-0002" sec-type="section"> <title>Methods</title> <p>Mice received hydrodynamically delivered HGF plasmid or control plasmid and then infected with adenovirus, and parameters of immune‐mediated liver damage were evaluated. We studied dendritic cell (DC) activation in the presence of HGF. T cells collected from infected mice were restimulated with virally infected DC to measure cytokine production <italic>in vitro</italic>.</p> </sec> <sec id="jgh12456-sec-0003" sec-type="section"> <title>Results</title> <p>HGF ameliorated the liver inflammation during viral hepatitis as alanine transferase, intrahepatic lymphocytes, and splenocyte counts were diminished by HGF. Lower histological scores of liver pathology were observed in the HGF group. DC from the HGF group expressed reduced CD40. The hepatic expression and serum concentration of IL‐12p40 were diminished in HGF‐transfected mice. <italic>In vitro</italic> experiments with DC confirmed that HGF diminished CD40 expression and IL‐12p40 production. The expression and serum levels of IFN‐γ, IL‐6 and CXCL9 were significantly decreased in the HGF group. HGF overexpression diminished the expression and concentration of IL‐10 and TGF‐β. The frequency of PD‐1<sup>+</sup>Tim‐3<sup>+</sup> in CD8 T cells was decreased by HGF overexpression. Moreover, T cells in the HGF group at day 14 secreted more IFN‐γ and TNF‐α than those in the control group when restimulated with virally infected DC.</p> </sec> <sec id="jgh12456-sec-0004" sec-type="section"> <title>Conclusion</title> <p>HGF modulated DC activation and T cell priming, thereby limiting the immune‐mediated damage in the liver. However, viral clearance was not compromised by HGF.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of gastroenterology and hepatology. Volume 29:Issue 4(2014:Apr.)
- Journal:
- Journal of gastroenterology and hepatology
- Issue:
- Volume 29:Issue 4(2014:Apr.)
- Issue Display:
- Volume 29, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 29
- Issue:
- 4
- Issue Sort Value:
- 2014-0029-0004-0000
- Page Start:
- 878
- Page End:
- 886
- Publication Date:
- 2014-04
- Subjects:
- Gastroenterology -- Periodicals
Digestive organs -- Diseases -- Periodicals
Liver -- Diseases -- Periodicals
Gastroenterology -- Periodicals
Liver Diseases -- Periodicals
616.33 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1440-1746 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/jgh ↗ - DOI:
- 10.1111/jgh.12456 ↗
- Languages:
- English
- ISSNs:
- 0815-9319
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4987.615000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3473.xml