Research Article
J Mol Genet Med (November 2006), 2(1), 93-100
doi: jmgm
Published online: 12 April 2006
Full Text: (html | pdf ~824kb | refs)
Rat activin-bE mRNA expression during development and in acute and chronic liver injury
Elspeth J Gold †*, Marcel A Monaghan ‡ and Jean S Fleming §
† Centre for Urological Research, Monash Institute of Medical Research, Monash University, Clayton, Victoria 3168, Australia
‡ Department of Anatomy and Structural Biology, University of Otago, School of Medical Sciences, Dunedin, New Zealand
§ Eskitis Institute of Cell & Molecular Therapies, School of Biomolecular and Biomedical Sciences, Griffith University, Nathan Campus, Nathan, QLD 4111, Australia
*Correspondence to: Elspeth J Gold, Email:elspeth.gold@med.monash.edu.au, Tel: +613 9594 7129 , Fax: +613 9594 7115
Received: 17 January 2006, Revised: 06 March 2006, Accepted: 08 March 2006
© Copyright The Authors
-----------------------------------------------------------------------------------------------------------------
ABSTRACT
Activin-b E mRNA expression was investigated in male and female rats using gel-based and quantitative RT-PCR, in fetal and post-natal liver during development and in a variety of tissues from 200 gm adult animals. Activin- b E expression was also assessed in rat liver after partial hepatectomy, and after repeated toxic insult. Male Sprague Dawley rats were subjected to partial hepatectomy or sham operations. Samples were collected from the caudate liver lobe during regeneration, from 12 to 240 hr after surgery. Three groups of 5 male rats were treated with CCl 4 for 0 (control), 5 or 10 weeks, to induce liver fibrosis and cirrhosis. Activin-bE mRNA was predominantly expressed in liver, with much lower amounts of mRNA observed in pituitary, adrenal gland and spleen, in both males and females. Low activin-bE expression was observed in liver at fetal day 16, with higher levels seen between post-natal days 3 and 35 and a further increase noted by day 47, in both males and females. Liver activin-bE mRNA concentrations did not change from control values 12-72 hr after PHx, but significantly increased over six fold, 168 hr post-hepatectomy, when liver mass was restored. Activin-bE mRNA was up-regulated after 5 weeks of CCl 4 treatment, but not after 10 weeks. The changes in activin-bE mRNA concentrations after liver insult did not always parallel those reported for the activin-bC subunit, suggesting activin-bE may have an independent role in liver under certain conditions.
KEYWORDS: Activin-bE, liver, cirrhosis, hepatectomy, development
-----------------------------------------------------------------------------------------------------------------
Privacy | Disclaimer
©Library Publishing Media. All rights reserved. |