a Department of Pharmacology , School of Medicine, Southeast University , Nanjing , Jiangsu , China.
b Department of Emergency , Jiangsu Province Hospital and The First Affiliated Hospital of Nanjing Medical University , Nanjing , Jiangsu , China.
Autophagy. 2018;14(7):1164-1184. doi: 10.1080/15548627.2018.1458173. Epub 2018 Jul 20.
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.
3-MA: 3-methyladenine; ACTB: actin beta; AIS: acute ischemic stroke; AS: primary mouse astrocytes; BECN1: beclin 1, autophagy related; BMI: body mass index; circHECTD1: circRNA HECTD1; circRNAs: circular RNAs; CBF: cerebral blood flow; Con: control; DAPI: 4',6-diamidino-2-phenylindole; ECA: external carotid artery; FISH: fluorescence in situ hybridization; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; Gdna: genomic DNA; GFAP: glial fibrillary acidic protein; GO: gene ontology; HDL: high-density lipoprotein; IOD: integrated optical density; LDL: low-density lipoprotein; LPA: lipoprotein(a); MAP1LC3B: microtubule-associated protein 1 light chain 3 beta; MIR142: microRNA 142; mNSS: modified neurological severity scores; MRI: magnetic resonance imaging; NIHSS: National Institute of Health Stoke Scale; OGD-R: oxygen glucose deprivation-reperfusion; PCR: polymerase chain reaction; PFA: paraformaldehyde; SQSTM1: sequestosome 1; TIPARP: TCDD inducible poly(ADP-ribose) polymerase; tMCAO: transient middle cerebral artery occlusion; TTC: 2,3,5-triphenyltetrazolium chloride; UTR: untranslated region; WT: wild type.
环状 RNA(circRNAs)在中枢神经系统中高度表达,并参与生理和病理生理过程的调节。然而,circRNAs 在中风中的潜在作用在很大程度上仍然未知。在这里,我们使用环状 RNA 微阵列显示,circRNA Hectd1(circHectd1)水平在短暂性大脑中动脉闭塞(tMCAO)小鼠中风模型的缺血性脑组织中显著增加,并在急性缺血性中风(AIS)患者的血浆样本中进一步验证了这一发现。circHectd1 表达的敲低显著减少了梗死面积,减轻了 tMCAO 小鼠的神经元缺失,并改善了星形胶质细胞的激活。机制上,circHECTD1 作为内源性 MIR142(microRNA 142)海绵,抑制 MIR142 活性,导致 TIPARP(TCDD 诱导的多[ADP-核糖]聚合酶)表达的抑制,随后通过巨自噬/自噬抑制星形胶质细胞的激活。总之,我们的研究结果表明,circHECTD1 及其偶联机制参与了脑缺血,从而提供了转化证据,表明 circHECTD1 可以作为中风的新型生物标志物和治疗靶点。
3-MA:3-甲基腺嘌呤;ACTB:肌动蛋白β;AIS:急性缺血性中风;AS:原代小鼠星形胶质细胞;BECN1:自噬相关的 beclin 1;BMI:体重指数;circHECTD1:环状 RNA HECTD1;circRNAs:环状 RNA;CBF:脑血流;Con:对照;DAPI:4',6-二脒基-2-苯基吲哚;ECA:颈外动脉;FISH:荧光原位杂交;GAPDH:甘油醛-3-磷酸脱氢酶;Gdna:基因组 DNA;GFAP:神经胶质纤维酸性蛋白;GO:基因本体论;HDL:高密度脂蛋白;IOD:整合光密度;LDL:低密度脂蛋白;LPA:脂蛋白(a);MAP1LC3B:微管相关蛋白 1 轻链 3β;MIR142:microRNA 142;mNSS:改良神经功能缺损评分;MRI:磁共振成像;NIHSS:国立卫生研究院中风量表;OGD-R:氧葡萄糖剥夺-再灌注;PCR:聚合酶链反应;PFA:多聚甲醛;SQSTM1:自噬体 1;TIPARP:TCDD 诱导的多(ADP-核糖)聚合酶;tMCAO:短暂性大脑中动脉闭塞;TTC:2,3,5-三苯基氯化四氮唑;UTR:非翻译区;WT:野生型。