Circ_0007706 downregulation ameliorates neonatal hypoxic ischemic encephalopathy via regulating the miR-579-3p/TRAF6 axis

被引:3
|
作者
Wang, Jinguang [1 ]
Hua, Minmin [1 ]
Li, Huixin [2 ]
Xu, Dan [3 ]
Li, Fangfang [4 ]
Xu, Falin [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 3, Dept Neonatol, 7 Kangfuqian St, Zhengzhou 450052, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Anesthesiol, Zhengzhou 450052, Peoples R China
[3] Zhengzhou Univ, Affiliated Hosp 3, Dept Neurol, Zhengzhou 450052, Peoples R China
[4] Zhengzhou Univ, Affiliated Hosp 3, Dept Resp Med, Zhengzhou 450052, Peoples R China
关键词
Neonatal hypoxic ischemic encephalopathy; Circ_0007706; miR-579-3p; TRAF6; INDUCED NEUROINFLAMMATION; BRAIN-INJURY; MECHANISMS;
D O I
10.1016/j.brainresbull.2023.01.013
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Neonatal hypoxic ischemic encephalopathy (HIE) is a main factor of neonatal death and permanent neurologic deficit. This study sought to investigate the functional role of hsa_circ_0007706 (circ_0007706) in modulating neonatal HIE.Methods: In vitro HIE cell model was established in hBMVECs under the condition of oxygen-glucose deprivation/ reperfusion (OGD/R) treatment. qRT-PCR analysis was utilized for detecting the level of circ_0007706, micro -RNA-579-3p (miR-579-3p) and TNF receptor-associated factor 6 (TRAF6). RNase R treatment and Oligo (dT) 18 primers were employed to verify the features of circ_0007706, and nucleocytoplasmic separation was conducted for determining the location of circ_0007706. CCK-8 assay, EdU assay, and flow cytometry were carried out to measure cell proliferation and apoptosis, respectively. The protein expression of Bax, Bcl-2 and TRAF6 was detected using western blot. Meanwhile, the levels of the pro-inflammatory factors were determined via ELISA. SOD activity and MDA level were assessed via the respective kits. Besides, dual-luciferase reporter assay and RNA pull-down were used to identify the association between miR-579-3p and circ_0007706 or TRAF6. Results: Circ_0007706 was elevated in HIE newborns and OGD/R cell model. Knockdown of circ_0007706 greatly alleviated OGD/R-induced injury, inflammatory response and oxidative stress. We found that miR-579-3p was a direct target of circ_0007706, and miR-579-3p inhibitor could reverse the impact of circ_0007706 knockdown on OGD/R-caused cell damage in hBMVECs. In addition, miR-579-3p directly interacted with TRAF6, and the protective effects of miR-579-3p on OGD/R-induced injury in hBMVECs were harbored by TRAF6 over -expression. Our data indicated that circ_0007706 knockdown could downregulate the expression of TRAF6 by sponging miR-579-3p in OGD/R-treated hBMVECs.Conclusion: This study demonstrated that circ_0007706 knockdown assuaged HIE-induced injury by decreasing TRAF6 expression via targeting miR-579-3p.
引用
收藏
页码:90 / 99
页数:10
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