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高迁移率族蛋白B1在斯-韦综合征患者脑组织中的高表达

High Translocation of High Mobility Group Box 1 in the Brain Tissue of Patients with Sturge-Weber Syndrome.

作者信息

Cheng Zizhang, Li Xiaoli, Wang Shu, Sun Weijin, Pan Junhong, Wang Xiongfei, Zhou Jian, Li Tianfu, Luan Guoming, Guan Yuguang

机构信息

Department of Neurosurgery, SanBo Brain Hospital, Capital Medical University, Beijing, 100093, People's Republic of China.

Department of Neurology, Affiliated Zhong Da Hospital, Southeast University, Nanjing, People's Republic of China.

出版信息

J Inflamm Res. 2024 Nov 21;17:9347-9358. doi: 10.2147/JIR.S473377. eCollection 2024.

Abstract

PURPOSE

Sturge-Weber syndrome (SWS), a rare congenital neurological and skin disorder, is frequently associated with drug-resistant epilepsy. Translocation of high mobility group box 1 (HMGB1) protein from the nucleus to the cytoplasm or extracellular milieu has been implicated in neuroinflammatory processes contributing to the development of epileptogenesis. This study aimed to explore the expression and distribution of HMGB1 in brain tissue from SWS patients with drug-resistant epilepsy, with the goal of elucidating its potential involvement in the pathogenesis of epilepsy.

PATIENTS AND METHODS

The study enrolled eight patients with drug-resistant epilepsy who underwent hemispherectomy. Brain tissue specimens were obtained and analyzed using immunofluorescence staining to detect HMGB1 distribution in microglia, astrocytes, or different neuronal subtypes. Correlation analyses were performed to investigate the potential relationship between HMGB1 translocation within cells and the clinical characteristics of SWS patients.

RESULTS

In lesional tissues of SWS patients, we observed significantly higher cytoplasmic HMGB1 levels. Meanwhile, HMGB1 was widely distributed in the cytoplasm of microglia and neurons, while in astrocytes, it was primarily localized in the nucleus. This translocation occurred across many neuronal subtypes, including excitatory glutamatergic, inhibitory GABAergic, and cholinergic neurons. The lower proportion of HMGB1-translocated cholinergic neurons was seen compared to the other two neuronal subtypes. Furthermore, no correlation was found between cytoplasmic HMGB1 levels and clinical characteristics of SWS patients.

CONCLUSION

The results suggest the involvement of HMGB1 in the pathogenesis of drug-resistant epilepsy in SWS patients. Additional research is required to elucidate the precise mechanisms and potential therapeutic targets associated with HMGB1 that underlie the epilepsy linked to SWS.

摘要

目的

斯特奇-韦伯综合征(SWS)是一种罕见的先天性神经和皮肤疾病,常与药物难治性癫痫相关。高迁移率族蛋白B1(HMGB1)从细胞核向细胞质或细胞外环境的转位与促成癫痫发生发展的神经炎症过程有关。本研究旨在探讨HMGB1在药物难治性癫痫的SWS患者脑组织中的表达和分布,以阐明其在癫痫发病机制中的潜在作用。

患者和方法

本研究纳入了8例接受大脑半球切除术的药物难治性癫痫患者。获取脑组织标本并使用免疫荧光染色进行分析,以检测HMGB1在小胶质细胞、星形胶质细胞或不同神经元亚型中的分布。进行相关性分析以研究细胞内HMGB1转位与SWS患者临床特征之间的潜在关系。

结果

在SWS患者的病变组织中,我们观察到细胞质中HMGB1水平显著升高。同时,HMGB1广泛分布于小胶质细胞和神经元的细胞质中,而在星形胶质细胞中,它主要定位于细胞核。这种转位发生在许多神经元亚型中,包括兴奋性谷氨酸能神经元、抑制性γ-氨基丁酸能神经元和胆碱能神经元。与其他两种神经元亚型相比,HMGB1转位的胆碱能神经元比例较低。此外,未发现细胞质中HMGB1水平与SWS患者的临床特征之间存在相关性。

结论

结果表明HMGB1参与了SWS患者药物难治性癫痫的发病机制。需要进一步研究以阐明与HMGB1相关的精确机制和潜在治疗靶点,这些机制和靶点是SWS相关癫痫的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/11587792/418df3859643/JIR-17-9347-g0001.jpg

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