KDM4A facilitates neuropathic pain and microglial M1 polarization by regulating BDNF in a rat model of brachial plexus avulsion.

IF 5.1 2区 医学 Q1 ANESTHESIOLOGY
Jinding Guo, Kaiming Gao, Xi Chen, Chengppeng Liao, Jing Rui, Yingjie Zhou, Jie Lao
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引用次数: 0

Abstract

Background: Many patients with brachial plexus avulsion (BPA) suffer from neuropathic pain, but the mechanism remains elusive. Modifications of histones, the proteins responsible for organizing DNA, may play an important role in neuropathic pain. Lysine demethylase 4A (KDM4A), an essential component of histone demethylase, can modify the function of chromatin and thus regulate the vital gene expressions. However, the mechanism by which KDM4A regulates neuropathic pain following BPA remains unclear.

Methods: The pain model was developed in adult rats that received BPA surgery. Western blot, ELISA, and reverse transcription-PCR were used to examine the protein and mRNA levels of targeted genes. Immunofluorescence studies were conducted to analyze their cellular distribution in the spinal cord. Pharmacological and genetic methods were used to modulate the expression of KDM4A. Co-immunoprecipitation and chromatin immunoprecipitation PCR were used to assess the binding potential between KDM4A and the promoter of brain-derived neurotrophic factor (BDNF).

Results: KDM4A and BDNF levels were significantly upregulated in the ipsilateral spinal cord dorsal horn in the BPA group compared with the sham surgery group. Additionally, knockdown of KDM4A decreased BDNF expression and microgliosis and reduced neuropathic pain-like behaviors in BPA rats. Conversely, KDM4A overexpression increased BDNF expression and microgliosis and exacerbated neuropathic pain. BDNF inhibitors and activators also regulated the activation of spinal microglia and neuropathic pain. Importantly, we showed that KDM4A modulates BDNF expression by regulating the methylation of histone 3 lysine 9 and histone 3 lysine 36 in its promoter region.

Conclusion: Current findings suggest that the upregulation of KDM4A increases BDNF expression in the spinal cord in rats after BPA, contributing to microgliosis, neuroinflammation, and neuropathic pain.

在臂丛神经撕脱大鼠模型中,KDM4A通过调节BDNF促进神经性疼痛和小胶质细胞M1极化。
背景:许多臂丛神经撕脱伤(BPA)患者都会出现神经病理性疼痛,但其机制仍然难以捉摸。组蛋白是负责组织 DNA 的蛋白质,其修饰可能在神经性疼痛中扮演重要角色。赖氨酸去甲基化酶 4A(KDM4A)是组蛋白去甲基化酶的重要组成部分,可以改变染色质的功能,从而调节重要基因的表达。然而,KDM4A调节双酚A引起的神经病理性疼痛的机制仍不清楚:方法:在接受过双酚 A 手术的成年大鼠中建立疼痛模型。Western印迹、ELISA和反转录-PCR用于检测目标基因的蛋白和mRNA水平。免疫荧光研究分析了目标基因在脊髓中的细胞分布。采用药理学和遗传学方法调节 KDM4A 的表达。共免疫沉淀和染色质免疫沉淀 PCR 被用来评估 KDM4A 与脑源性神经营养因子(BDNF)启动子之间的结合潜力:结果:与假手术组相比,双酚A组同侧脊髓背角的KDM4A和BDNF水平明显上调。此外,敲除 KDM4A 会降低 BPA 大鼠的 BDNF 表达和微神经胶质细胞增生,并减少神经病理性疼痛样行为。相反,KDM4A的过表达会增加BDNF的表达和小神经胶质细胞的增生,并加剧神经病理性疼痛。BDNF 抑制剂和激活剂也能调节脊髓小胶质细胞的激活和神经病理性疼痛。重要的是,我们发现 KDM4A 通过调节 BDNF 启动子区域组蛋白 3 赖氨酸 9 和组蛋白 3 赖氨酸 36 的甲基化来调节 BDNF 的表达:目前的研究结果表明,KDM4A 的上调会增加双酚 A 后大鼠脊髓中 BDNF 的表达,从而导致小神经胶质细胞增多、神经炎症和神经病理性疼痛。
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来源期刊
CiteScore
8.50
自引率
11.80%
发文量
175
审稿时长
6-12 weeks
期刊介绍: Regional Anesthesia & Pain Medicine, the official publication of the American Society of Regional Anesthesia and Pain Medicine (ASRA), is a monthly journal that publishes peer-reviewed scientific and clinical studies to advance the understanding and clinical application of regional techniques for surgical anesthesia and postoperative analgesia. Coverage includes intraoperative regional techniques, perioperative pain, chronic pain, obstetric anesthesia, pediatric anesthesia, outcome studies, and complications. Published for over thirty years, this respected journal also serves as the official publication of the European Society of Regional Anaesthesia and Pain Therapy (ESRA), the Asian and Oceanic Society of Regional Anesthesia (AOSRA), the Latin American Society of Regional Anesthesia (LASRA), the African Society for Regional Anesthesia (AFSRA), and the Academy of Regional Anaesthesia of India (AORA).
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