| Literature DB >> 28342874 |
Dan Wang1, Liuyan Shi2, Wei Xin3, Jiancheng Xu1, Jing Xu1, Qi Li1, Zhi Xu1, Jianchun Wang1, Guansong Wang1, Wei Yao1, Binfeng He1, Yu Yang1, Mingdong Hu4.
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.Entities:
Keywords: Inflammation; Inflammatory cytokines; PPARγ; miR-124
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Year: 2017 PMID: 28342874 DOI: 10.1016/j.bbrc.2017.03.106
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575