| Literature DB >> 28593745 |
Dongdong Jian1, Bing Dai1, Xiaotong Hu2, Qiang Yao3, Chengfei Zheng1, Jianhua Zhu1.
Abstract
Macrophages and oxidized low-density lipoprotein (ox-LDL) have been verified playing vital roles in the pathogenesis of atherosclerosis (AS). Previous studies demonstrated that microRNA-29a (miR-29a) was upregulated in many atherogenic process and cells, thus acting as an important participant in AS. But the detailed regulation mechanism of miR-29a in AS has not been fully understood. In our study, we demonstrated a positive feedback loop of ox-LDL-SRA-miR-29a. Furthermore, we found that YY1 and STAT1 were upregulated in ox-LDL-stimulating macrophages followed by translocation in the nucleus and binding to the transcriptional promoter region of miR-29a, thus leading to the increase of miR-29a expression. In addition, we demonstrated that JAK1/2 signaling was involved in miR-29a upregulation. Finally, we found that miR-29a played important roles in the secretion of proinflammation factors and lipid uptake in macrophages. We uncovered the molecular mechanism and provide novel insights into the function and regulatory network of miR-29a expression regulated by ox-LDL in macrophages.Entities:
Keywords: STAT1; YY1; macrophages; miR-29a; ox-LDL
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Year: 2017 PMID: 28593745 DOI: 10.1002/cbin.10803
Source DB: PubMed Journal: Cell Biol Int ISSN: 1065-6995 Impact factor: 3.612