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Liver microRNA-21 is overexpressed in non-alcoholic steatohepatitis and contributes to the disease in experimental models by inhibiting PPARα expression.
- Source :
-
Gut [Gut] 2016 Nov; Vol. 65 (11), pp. 1882-1894. Date of Electronic Publication: 2015 Sep 03. - Publication Year :
- 2016
-
Abstract
- Objective: Previous studies suggested that microRNA-21 may be upregulated in the liver in non-alcoholic steatohepatitis (NASH), but its role in the development of this disease remains unknown. This study aimed to determine the role of microRNA-21 in NASH.<br />Design: We inhibited or suppressed microRNA-21 in different mouse models of NASH: (a) low-density lipoprotein receptor-deficient ( Ldlr <superscript>-/-</superscript> ) mice fed a high-fat diet and treated with antagomir-21 or antagomir control; (b) microRNA-21-deficient and wild-type mice fed a methionine-choline-deficient (MCD) diet; (c) peroxisome proliferation-activator receptor α (PPARα)-deficient mice fed an MCD diet and treated with antagomir-21 or antagomir control. We assessed features of NASH and determined liver microRNA-21 levels and cell localisation. MicroRNA-21 levels were also quantified in the liver of patients with NASH, bland steatosis or normal liver and localisation was determined.<br />Results: Inhibiting or suppressing liver microRNA-21 expression reduced liver cell injury, inflammation and fibrogenesis without affecting liver lipid accumulation in Ldlr <superscript>-/-</superscript> fed a high-fat diet and in wild-type mice fed an MCD diet. Liver microRNA-21 was overexpressed, primarily in biliary and inflammatory cells, in mouse models as well as in patients with NASH, but not in patients with bland steatosis. PPARα, a known microRNA-21 target, implicated in NASH, was decreased in the liver of mice with NASH and restored following microRNA-21 inhibition or suppression. The effect of antagomir-21 was lost in PPARα-deficient mice.<br />Conclusions: MicroRNA-21 inhibition or suppression decreases liver injury, inflammation and fibrosis, by restoring PPARα expression. Antagomir-21 might be a future therapeutic strategy for NASH.<br /> (Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.)
- Subjects :
- Animals
Diet, High-Fat
Gene Expression Profiling methods
Hepatocytes metabolism
Hepatocytes pathology
Humans
Lipid Metabolism
Lipoproteins, LDL metabolism
Mice
MicroRNAs antagonists & inhibitors
PPAR alpha antagonists & inhibitors
MicroRNAs metabolism
Non-alcoholic Fatty Liver Disease metabolism
Non-alcoholic Fatty Liver Disease prevention & control
Oligonucleotides metabolism
Oligonucleotides pharmacology
PPAR alpha metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1468-3288
- Volume :
- 65
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Gut
- Publication Type :
- Academic Journal
- Accession number :
- 26338827
- Full Text :
- https://doi.org/10.1136/gutjnl-2014-308883