揭示H3k9me2参与颈内动脉闭塞小鼠模型神经炎症、损伤和恢复的性别特异性表观遗传调控机制

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Mydhili Radhakrishnan, Vincy Vijay, B Supraja Acharya, Papia Basuthakur, Shashikant Patel, Kalyani Soren, Arvind Kumar, Sumana Chakravarty
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引用次数: 0

摘要

脑缺血中风是全球最主要的死亡和残疾原因之一。由于对缺血性脑卒中的发病机制认识不足,减轻急性缺血性脑卒中所致脑损伤的治疗手段十分有限。最近的研究表明,表观遗传机制(主要是组蛋白赖氨酸乙酰化/去乙酰化)与缺血诱导的神经损伤和死亡有关。然而,赖氨酸甲基化/去甲基化是脑缺血中另一种普遍存在的表观遗传机制,除了最近的一些报道(包括我们研究队列的报道)外,尚未对其作用进行全面调查。考虑到性别对卒中后预后的影响,我们利用最近开发的颈内动脉闭塞(ICAO)模型对雌雄小鼠进行了研究,以阐明其分子细节,该模型可诱导轻中度脑缺血,主要影响纹状体和海马腹侧。在此,我们首次证明,通过神经功能缺损评分和运动协调性评估,雌性小鼠在ICAO后的恢复速度快于雄性小鼠。此外,我们的研究还发现,组蛋白赖氨酸去甲基化酶(KDMs),尤其是 kdm4b/jmjd2b 的失调是导致炎症基因的性别特异性调节差异的原因。基于我们之前通过 DMOG(二甲基氧丙基甘氨酸)阻断 KDMs 从而防止 H3k9me2 的衰减降低了 ICAO 后炎症分子的转录水平和神经损伤的报道,我们目前的研究深入探讨了 H3k9me2 在调节雌性与雄性小鼠的促炎症基因中的不同作用,这也是 ICAO 诱导的神经损伤和恢复的基础。总之,我们的研究结果揭示了表观遗传标记 H3k9me2 在介导 ICAO 后诱发的炎症反应的性别特异性序列事件中的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Uncovering Sex-Specific Epigenetic Regulatory Mechanism Involving H3k9me2 in Neural Inflammation, Damage, and Recovery in the Internal Carotid Artery Occlusion Mouse Model.

Uncovering Sex-Specific Epigenetic Regulatory Mechanism Involving H3k9me2 in Neural Inflammation, Damage, and Recovery in the Internal Carotid Artery Occlusion Mouse Model.

Cerebral ischemic stroke is one of the foremost global causes of death and disability. Due to inadequate knowledge in its sequential disease mechanisms, therapeutic efforts to mitigate acute ischemia-induced brain injury are limited. Recent studies have implicated epigenetic mechanisms, mostly histone lysine acetylation/deacetylation, in ischemia-induced neural damage and death. However, the role of lysine methylation/demethylation, another prevalent epigenetic mechanism in cerebral ischemia has not undergone comprehensive investigation, except a few recent reports, including those from our research cohort. Considering the impact of sex on post-stroke outcomes, we studied both male and female mice to elucidate molecular details using our recently developed Internal Carotid Artery Occlusion (ICAO) model, which induces mild to moderate cerebral ischemia, primarily affecting the striatum and ventral hippocampus. Here, we demonstrate for the first time that female mice exhibit faster recovery than male mice following ICAO, evaluated through neurological deficit score and motor coordination assessment. Furthermore, our investigation unveiled that dysregulated histone lysine demethylases (KDMs), particularly kdm4b/jmjd2b are responsible for the sex-specific variance in the modulation of inflammatory genes. Building upon our prior reportage blocking KDMs by DMOG (Dimethyloxalylglycine) and thus preventing the attenuation in H3k9me2 reduced the post-ICAO transcript levels of the inflammatory molecules and neural damage, our present study delved into investigating the differential role of H3k9me2 in the regulation of pro-inflammatory genes in female vis-à-vis male mice underlying ICAO-induced neural damage and recovery. Overall, our results reveal the important role of epigenetic mark H3k9me2 in mediating sex-specific sequential events in inflammatory response, elicited post-ICAO.

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