circCCDC6与microRNA-128-3p的竞争性结合激活TXNIP/NLRP3通路并促进脑缺血再灌注缺陷。

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
ChongShu Wang, MingMing Dong, XiaoYi Zhang, XiaoYu Wang, Yan Zhao, Yunpeng Cao
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引用次数: 0

摘要

目的:环状核糖核酸(circRNAs)在大脑中富集,并与各种中枢神经系统疾病有关。circCCDC6在脑缺血再灌注缺陷中的潜在作用在该工作中得到了部分阐明。方法:建立大鼠大脑中动脉闭塞/再灌注(MCAO/R)模型和糖氧剥夺再氧合(OGD/R)处理的SH-SY5Y细胞模型。检测了两种模型中CircCCDCC6的表达,并通过功能丧失和获得测定分析了CircCCDC6参与神经元焦下垂和炎症的机制。结果:MCAO/R大鼠脑组织和OGD/R处理的SH-SY5Y细胞的circCCDC6表达上调。CIRCDCD6的沉默减轻了MCAO/R大鼠脑组织中的神经元焦下垂和炎症。过度表达circCCDC6或抑制miR-128-3p刺激了OGD/R诱导的SH-SY5Y细胞的pyroptosis和炎症,而上调miR-128-3p减轻了OGD/R损伤。CircCCDCC6对SH-SY5Y细胞的沉默诱导作用被TXNIP过表达所拮抗。结论:从机制上讲,circCCDC6介导miR-128-3p并激活TXNIP/NLRP3,从而促进OGD/R诱导的神经元焦下垂和炎症。CircCCDC6可能为MCAO/R的治疗提供一种新的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Competitive binding of circCCDC6 to microRNA-128-3p activates TXNIP/NLRP3 pathway and promotes cerebral ischemia-reperfusion defects.

Objective: Circular RNAs (circRNAs) are enriched in the brain and involved in various central nervous system diseases. The potential role of circCCDC6 in cerebral ischemia-reperfusion defects was partly elucidated in the work.

Methods: A middle cerebral artery occlusion/reperfusion (MCAO/R) rat model and an oxygen-glucose deprivation and re-oxygenation (OGD/R)-treated SH-SY5Y cell model were constructed. CircCCDC6 expression in the two models was examined, and circCCDC6-involved mechanisms in neuronal pyroptosis and inflammation were analyzed through loss- and gain-of-function assays.

Results: MCAO/R rat brain tissues and OGD/R-treated SH-SY5Y cells exhibited upregulated circCCDC6. Silencing circCCDC6 attenuated neuronal pyroptosis and inflammation in the brain tissue of MCAO/R rats. Overexpressing circCCDC6 or inhibiting miR-128-3p stimulated OGD/R-induced pyroptosis and inflammation in SH-SY5Y cells, while upregulating miR-128-3p attenuated OGD/R injury. CircCCDC6 silencing-induced effects on SH-SY5Y cells were antagonized by TXNIP overexpression.

Conclusion: Mechanistically, circCCDC6 mediates miR-128-3p and activates TXNIP/NLRP3, thereby promoting OGD/R-induced neuronal pyroptosis and inflammation. CircCCDC6 may provide a new strategy for the treatment of MCAO/R.

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来源期刊
Acta biochimica Polonica
Acta biochimica Polonica 生物-生化与分子生物学
CiteScore
2.40
自引率
0.00%
发文量
99
审稿时长
4-8 weeks
期刊介绍: Acta Biochimica Polonica is a journal covering enzymology and metabolism, membranes and bioenergetics, gene structure and expression, protein, nucleic acid and carbohydrate structure and metabolism.
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