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Activation of PPARγ inhibits pro-inflammatory cytokines production by upregulation of miR-124 in vitro and in vivo.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2017 May 06; Vol. 486 (3), pp. 726-731. Date of Electronic Publication: 2017 Mar 22. - Publication Year :
- 2017
-
Abstract
- Peroxisome proliferator-activated receptor gamma (PPARγ) and miR-124 have been reported to play important roles in regulation of inflammation. However, the underlying anti-inflammatory mechanisms remain not well understood. In the present study, we demonstrated that the expression level of PPARγ is positively correlated with that of miR-124 in patients with sepsis. Activation of PPARγ upregulates miR-124 and in turn inhibits miR-124 target gene. PPARγ bound directly to PPRE in the miR-124 promoter region, and enhanced the promoter transcriptional activity. PPARγ-induced miR-124 is involved in the suppression of pro-inflammatory cytokine in vitro and in vivo. These results suggest that PPARγ-induced miR-124 inhibits the production of pro-inflammatory cytokines is a novel PPARγ anti-inflammatory mechanism and also indicate that miR-124 may be a potential therapeutic target for the treatment of inflammatory diseases.<br /> (Copyright © 2017. Published by Elsevier Inc.)
- Subjects :
- Animals
Antagomirs genetics
Antagomirs metabolism
Binding Sites
Case-Control Studies
Cell Line
Gene Expression Regulation
Humans
Interleukin-6 genetics
Interleukin-6 metabolism
Lipopolysaccharides pharmacology
Macrophages drug effects
Macrophages pathology
Mice
Mice, Inbred BALB C
MicroRNAs agonists
MicroRNAs antagonists & inhibitors
MicroRNAs metabolism
PPAR gamma metabolism
Promoter Regions, Genetic
Protein Binding
Sepsis metabolism
Sepsis pathology
Signal Transduction
Tumor Necrosis Factor-alpha genetics
Tumor Necrosis Factor-alpha metabolism
Macrophages metabolism
MicroRNAs genetics
PPAR gamma genetics
Sepsis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 486
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 28342874
- Full Text :
- https://doi.org/10.1016/j.bbrc.2017.03.106