Circular RNA DLGAP4 Ameliorates Ischemic Stroke Outcomes by Targeting miR-143 to Regulate Endothelial-Mesenchymal Transition Associated with Blood-Brain Barrier Integrity

被引:409
作者
Bai, Ying [1 ]
Zhang, Yuan [1 ]
Han, Bing [1 ]
Yang, Li [1 ]
Chen, Xufeng [2 ]
Huang, Rongrong [1 ]
Wu, Fangfang [1 ]
Chao, Jie [3 ]
Liu, Pei [4 ]
Hu, Gang [5 ]
Zhang, John H. [6 ]
Yao, Honghong [1 ,7 ]
机构
[1] Southeast Univ, Sch Med, Dept Pharmacol, Nanjing 210009, Jiangsu, Peoples R China
[2] Jiangsu Prov Hosp, Emergency Dept, Nanjing 210029, Jiangsu, Peoples R China
[3] Southeast Univ, Sch Med, Dept Physiol, Nanjing 210009, Jiangsu, Peoples R China
[4] Southeast Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Nanjing 210009, Jiangsu, Peoples R China
[5] Nanjing Med Univ, Dept Pharmacol, Jiangsu Key Lab Neurodegenerat, Nanjing 210029, Jiangsu, Peoples R China
[6] Loma Linda Univ, Sch Med, Dept Anesthesiol, Loma Linda, CA 92354 USA
[7] Southeast Univ, Key Lab Dev Genes & Human Dis, Inst Life Sci, Nanjing 210096, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
blood-brain barrier integrity; circular RNA DLGAP4; endothelial-mesenchymal transition; ischemic stroke; miR-143; transient middle cerebral artery occlusion; FOCAL ADHESION DYNAMICS; HEPATOCELLULAR-CARCINOMA; MULTIPLE-SCLEROSIS; HEART-FAILURE; CELLS; INJURY; ACTIVATION; GROWTH; BETA; MICE;
D O I
10.1523/JNEUROSCI.1348-17.2017
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Circular RNAs (circRNAs) are highly expressed in the CNS and regulate physiological and pathophysiological processes. However, the potential role of circRNAs in stroke remains largely unknown. Here, we show that the circRNA DLGAP4 (circDLGAP4) functions as an endogenous microRNA-143 (miR-143) sponge to inhibit miR-143 activity, resulting in the inhibition of homologous to the E6-AP C-terminal domain E3 ubiquitin protein ligase 1 expression. circDLGAP4 levels were significantly decreased in the plasma of acute ischemic stroke patients (13 females and 13 males) and in a mouse stroke model. Upregulation of circDLGAP4 expression significantly attenuated neurological deficits and decreased infarct areas and blood-brain barrier damage in the transient middle cerebral artery occlusion mouse stroke model. Endothelial-mesenchymal transition contributes to blood-brain barrier disruption and circDLGAP4 overexpression significantly inhibited endothelial-mesenchymal transition by regulating tight junction protein and mesenchymal cell marker expression. Together, the results of our study are illustrative of the involvement of circDLGAP4 and its coupling mechanism in cerebral ischemia, providing translational evidence that circDLGAP4 serves as a novel therapeutic target for acute cerebrovascular protection.
引用
收藏
页码:32 / 50
页数:19
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