Novel insight into circular RNA HECTD1 in astrocyte activation via autophagy by targeting MIR142-TIPARP: implications for cerebral ischemic stroke

被引:354
作者
Han, Bing [1 ]
Zhang, Yuan [1 ]
Zhang, Yanhong [1 ]
Bai, Ying [1 ]
Chen, Xufeng [2 ,3 ]
Huang, Rongrong [1 ]
Wu, Fangfang [1 ]
Leng, Shuo [4 ]
Chao, Jie [5 ]
Zhang, John H. [6 ]
Hu, Gang [7 ]
Yao, Honghong [1 ,8 ]
机构
[1] Southeast Univ, Sch Med, Dept Pharmacol, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Emergency, Jiangsu Prov Hosp, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[4] Southeast Univ, Sch Med, Dept Radiol, Nanjing, Jiangsu, Peoples R China
[5] Southeast Univ, Sch Med, Dept Physiol, Nanjing, Jiangsu, Peoples R China
[6] Loma Linda Univ, Sch Med, Dept Physiol & Pharmacol, Loma Linda, CA USA
[7] Nanjing Med Univ, Dept Pharmacol, Jiangsu Key Lab Neurodegenerat, Nanjing, Jiangsu, Peoples R China
[8] Southeast Univ, Key Lab Dev Genes & Human Dis, Inst Life Sci, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Astrocyte activation; autophagy; circHECTD1; MIR142; stroke; TIPARP; tMCAO; BRAIN-INJURY; MONITORING AUTOPHAGY; NEURONAL INJURY; UP-REGULATION; RAT MODEL; T-PA; NEUROPROTECTION; GENE; MIR-142-3P; EXPRESSION;
D O I
10.1080/15548627.2018.1458173
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Circular RNAs (circRNAs) are highly expressed in the central nervous system and are involved in the regulation of physiological and pathophysiological processes. However, the potential role of circRNAs in stroke remains largely unknown. Here, using a circRNA microarray, we showed that circular RNA Hectd1 (circHectd1) levels were significantly increased in ischemic brain tissues in transient middle cerebral artery occlusion (tMCAO) mouse stroke models and further validated this finding in plasma samples from acute ischemic stroke (AIS) patients. Knockdown of circHectd1 expression significantly decreased infarct areas, attenuated neuronal deficits, and ameliorated astrocyte activation in tMCAO mice. Mechanistically, circHECTD1 functions as an endogenous MIR142 (microRNA 142) sponge to inhibit MIR142 activity, resulting in the inhibition of TIPARP (TCDD inducible poly[ADP-ribose] polymerase) expression with subsequent inhibition of astrocyte activation via macroautophagy/autophagy. Taken together, the results of our study indicate that circHECTD1 and its coupling mechanism are involved in cerebral ischemia, thus providing translational evidence that circHECTD1 can serve as a novel biomarker of and therapeutic target for stroke.
引用
收藏
页码:1164 / 1184
页数:21
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