MicroRNA-128-3p Affects Neuronal Apoptosis and Neurobehavior in Cerebral Palsy Rats by Targeting E3 Ubiquitin-Linking Enzyme Smurf2 and Regulating YY1 Expression.

IF 4.6 2区 医学 Q1 NEUROSCIENCES Molecular Neurobiology Pub Date : 2025-02-01 Epub Date: 2024-08-05 DOI:10.1007/s12035-024-04362-7
Xiaoqi Nie, Rui Cheng, Pengfei Hao, Yuhong Guo, Gang Chen, Lei Ji, Lu Jia
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Abstract

This study was dedicated to investigating the effects of microRNA-128-3p (miR-128-3p) on neuronal apoptosis and neurobehavior in cerebral palsy (CP) rats via the Smurf2/YY1 axis.In vivo modeling of hypoxic-ischemic (HI) CP was established in neonatal rats. Neurobehavioral tests (geotaxis reflex, cliff avoidance reaction, and grip test) were measured after HI induction. The HI-induced neurological injury was evaluated by HE staining, Nissl staining, TUNEL staining, immunohistochemical staining, and RT-qPCR. The expression of miR-128-3p, Smurf2, and YY1 was determined by RT-qPCR and western blot techniques. Moreover, primary cortical neurons were used to establish the oxygen and glucose deprivation (OGD) model in vitro, cell viability was detected by CCK-8 assay, neuronal apoptosis was assessed by flow cytometry and western blot, and the underlying mechanism between miR-128-3p, Smurf2 and YY1 was verified by bioinformatics analysis, dual luciferase reporter assay, RIP, Co-IP, ubiquitination assay, western blot, and RT-qPCR.In vivo, miR-128-3p and YY1 expression was elevated, and Smurf2 expression was decreased in brain tissues of hypoxic-ischemic CP rats. Downregulation of miR-128-3p or overexpression of Smurf2 improved neurobehavioral performance, reduced neuronal apoptosis, and elevated Nestin and NGF expression in hypoxic-ischemic CP rats, and downregulation of Smurf2 reversed the effects of downregulation of miR-128-3p on neurobehavioral performance, neuronal apoptosis, and Nestin and NGF expression in hypoxic-ischemic CP rats, while overexpression of YY1 reversed the effects of Smurf2 on neurobehavioral performance, neuronal apoptosis, and Nestin and NGF expression in hypoxic-ischemic CP rats. In vitro, downregulation of miR-128-3p effectively promoted the neuronal survival, reduced the apoptosis rate, and decreased caspase3 protein expression after OGD, and overexpression of YY1 reversed the ameliorative effect of downregulation of miR-128-3p on OGD-induced neuronal injury. miR-128-3p targeted to suppress Smurf2 to lower YY1 ubiquitination degradation and decrease its expression.Inhibition of miR-128-3p improves neuronal apoptosis and neurobehavioral changes in hypoxic-ischemic CP rats by promoting Smurf2 to promote YY1 ubiquitination degradation and reduce YY1 expression.

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MicroRNA-128-3p通过靶向E3泛素连接酶Smurf2和调控YY1表达影响脑瘫大鼠神经元凋亡和神经行为
本研究致力于探讨microRNA-128-3p(miR-128-3p)通过Smurf2/YY1轴对脑瘫(CP)大鼠神经细胞凋亡和神经行为的影响。HI诱导后,对神经行为测试(地轴反射、悬崖回避反应和握力测试)进行了测量。通过 HE 染色、Nissl 染色、TUNEL 染色、免疫组化染色和 RT-qPCR 对 HI 诱导的神经损伤进行了评估。通过 RT-qPCR 和 Western 印迹技术测定了 miR-128-3p、Smurf2 和 YY1 的表达。此外,利用原代皮层神经元在体外建立氧和葡萄糖剥夺(OGD)模型,通过CCK-8检测细胞活力,通过流式细胞术和Western印迹评估神经元凋亡,并通过生物信息学分析、双荧光素酶报告实验、RIP、Co-IP、泛素化实验、Western印迹和RT-qPCR验证了miR-128-3p、Smurf2和YY1之间的内在机制。在缺氧缺血性 CP 大鼠体内,miR-128-3p 和 YY1 表达升高,Smurf2 表达降低。下调 miR-128-3p 或过表达 Smurf2 可改善缺氧缺血性 CP 大鼠的神经行为表现、减少神经元凋亡、提高 Nestin 和 NGF 的表达,而下调 Smurf2 可逆转下调 miR-128-3p 对神经行为表现的影响、而过表达 YY1 可逆转 Smurf2 对缺氧缺血性 CP 大鼠神经行为表现、神经元凋亡以及 Nestin 和 NGF 表达的影响。在体外,下调miR-128-3p能有效促进OGD后神经元的存活、降低凋亡率和减少caspase3蛋白的表达,而过表达YY1能逆转下调miR-128-3p对OGD诱导的神经元损伤的改善作用。miR-128-3p靶向抑制Smurf2以降低YY1泛素化降解并减少其表达,抑制miR-128-3p通过促进Smurf2以促进YY1泛素化降解并减少YY1表达,从而改善缺氧缺血CP大鼠神经元凋亡和神经行为变化。
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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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