miR-452-3p 靶向 HDAC3 抑制 p65 去乙酰化并激活蛛网膜下腔出血后早期脑损伤中的 NF-κB 信号通路

IF 1.5 4区 工程技术 Q3 MECHANICS
Journal of Mechanics Pub Date : 2022-10-01 Epub Date: 2022-06-01 DOI:10.1007/s12028-022-01509-z
Junti Lu, Xiaodong Huang, Aiping Deng, Hong Yao, Gao Wu, Na Wang, Hui Gui, Mojie Ren, Shiwen Guo
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引用次数: 0

摘要

研究目的蛛网膜下腔出血(SAH)是脑卒中的一种亚型,早期脑损伤(EBI)是导致其不良预后的一个因素。microRNA(miRNA)在脑中大量表达并参与脑损伤。本研究探讨了 miR-452-3p 对 SAH 后 EBI 的影响:方法:建立 SAH 小鼠模型,在模型建立 48 小时后检测 miR-452-3p 的表达。评估神经行为功能、血脑屏障通透性、脑含水量、神经元凋亡和炎症因子。氧血红蛋白诱导 SAH 细胞模型。检测了细胞凋亡率、乳酸脱氢酶和活性氧。研究验证了 miR-452-3p 与组蛋白去乙酰化酶 3(HDAC3)之间的靶向关系。检测了 p65 的乙酰化和 HDAC3 与 p65 的结合。检测到了核因子κB通路的抑制蛋白(IκBα)。向接受 miR-452-3p 抑制剂治疗的 SAH 小鼠注射羟肟酸苏贝酰苯胺:结果:SAH小鼠的miR-452-3p表达上调;神经系统评分降低;血脑屏障通透性、脑水含量和神经元凋亡增加;促炎因子升高;抗炎因子降低。SAH 增加了氧合血红蛋白处理的神经元细胞的凋亡率、乳酸脱氢酶释放量和活性氧水平。抑制 miR-452-3p 可逆转上述趋势。miR-452-3p 抑制剂促进了 HDAC3 与 p65 的结合,降低了 p65 的乙酰化,并上调了 IκBα。结论:miR-452-3p靶向HDAC3抑制p65的去乙酰化并激活核因子κB通路,从而加重了SAH后的脑损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
miR-452-3p Targets HDAC3 to Inhibit p65 Deacetylation and Activate the NF-κB Signaling Pathway in Early Brain Injury after Subarachnoid Hemorrhage.

Objectives: Subarachnoid hemorrhage (SAH) is a subtype of stroke, and early brain injury (EBI) is a contributor to its unfavorable outcome. microRNA (miRNA) is abundantly expressed in the brain and participates in brain injury. This study investigated the effect of miR-452-3p on EBI after SAH.

Methods: The murine model of SAH was established. miR-452-3p expression was detected 48 h after the model establishment. Neurobehavioral function, blood-brain barrier permeability, brain water content, neuronal apoptosis, and inflammatory factors were evaluated. The cell model of SAH was induced by oxygen hemoglobin. Apoptosis rate, lactate dehydrogenase, and reactive oxygen species were detected. The targeting relationship between miR-452-3p and histone deacetylase 3 (HDAC3) was verified. The acetylation of p65 and the binding of HDAC3 to p65 were detected. The inhibitory protein of the nuclear factor κB pathway (IκBα) was detected. Suberoylanilide hydroxamic acid was injected into the SAH mice treated with miR-452-3p inhibitor.

Results: SAH mice showed upregulated miR-452-3p expression; reduced the neurological score; increased blood-brain barrier permeability, brain water content, and neuronal apoptosis; elevated pro-inflammatory factors; and reduced anti-inflammatory factors. SAH increased the apoptosis rate, lactate dehydrogenase release, and reactive oxygen species levels in oxygen-hemoglobin-treated neuron cells. Inhibition of miR-452-3p reversed the above trends. miR-452-3p targeted HDAC3. SAH upregulated p65 acetylation. miR-452-3p inhibitor promoted the binding of HDAC3 to p65, decreased p65 acetylation, and upregulated IκBα. Suberoylanilide hydroxamic acid reversed the protective effect of miR-452-3p inhibitor on SAH mice and aggravated brain injury.

Conclusions: miR-452-3p targeted HDAC3 to inhibit the deacetylation of p65 and activate the nuclear factor κB pathway, thus aggravating EBI after SAH.

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来源期刊
Journal of Mechanics
Journal of Mechanics 物理-力学
CiteScore
3.20
自引率
11.80%
发文量
20
审稿时长
6 months
期刊介绍: The objective of the Journal of Mechanics is to provide an international forum to foster exchange of ideas among mechanics communities in different parts of world. The Journal of Mechanics publishes original research in all fields of theoretical and applied mechanics. The Journal especially welcomes papers that are related to recent technological advances. The contributions, which may be analytical, experimental or numerical, should be of significance to the progress of mechanics. Papers which are merely illustrations of established principles and procedures will generally not be accepted. Reports that are of technical interest are published as short articles. Review articles are published only by invitation.
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