MiRNA-203a-3p inhibits inflammatory response in preeclampsia through regulating IL24

被引:7
|
作者
Ma, H. -Y. [1 ]
Cu, W. [2 ]
Sun, Y. -H. [3 ]
Chen, X. [4 ]
机构
[1] Zibo Maternal & Child Hlth Hosp, Dept Obstet, Zibo, Peoples R China
[2] Yuhuangding Hosp Yantai, Dept Obstet Surg, Yantai, Peoples R China
[3] Rizhao Lanshan Peoples Hosp, Dept Gynaecol, Rizhao, Peoples R China
[4] Taian Cent Hosp, Dept Emergency, Tai An, Shandong, Peoples R China
关键词
MicroRNA-203a-3p; IL24; PE; Inflammatory response; POTENTIAL BIOMARKERS; PATHOGENESIS; GROWTH; ONSET;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: This study aims to investigate the protective role of miRNA-203a-3p in preeclampsia (PE) patients via inhibiting the inflammatory key protein IL24. PATIENTS AND METHODS: Serum samples of 36 PE pregnant women and 30 normal pregnant volunteers hospitalized between 2015 and 2019 were collected to extract placental mononuclear cells and exosomes. Relative levels of microRNA-203a-3p and IL24 were examined by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). In addition, the interaction between microRNA-203a-3p and IL24 was analyzed through bioinformatics analysis and Luciferase reporting assay. Finally, the underlying molecular mechanisms were further explored via immunofluorescence and Western blotting. RESULTS: Compared with normal pregnant volunteers, microRNA-203a-3p expression in serum exosomes and placental mononuclear cells of PE patients were dramatically reduced, while IL24 was conversely up-regulated, indicating a negative correlation between microRNA-203a-3p and IL24 levels. In addition, IL24, which was down-regulated in mononuclear macrophages overexpressing microRNA-203a-3p, was indicated as a target of microRNA-203a-3p. At the same time, microRNA-203a-3p was able to suppress the proliferation capacity of LPS-stimulated mononuclear macrophages, and it exerted anti-inflammatory effects via down-regulating IL24 in THP-1 cells. CONCLUSIONS: MicroRNA-203a-3p plays an anti-inflammatory role in PE pregnant women by down-regulating IL24 level.
引用
收藏
页码:5223 / 5230
页数:8
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