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基于蛋白质组学的散发性梅尼埃病患者外周血单个核细胞的潜在生物标志物。

Potential biomarkers in peripheral blood mononuclear cells of patients with sporadic Ménière's disease based on proteomics.

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiaotong University, Shanghai, China.

Shanghai Jiaotong University School of Medicine Ear Institute, Shanghai, China.

出版信息

Acta Otolaryngol. 2023 Aug;143(8):636-646. doi: 10.1080/00016489.2023.2241517. Epub 2023 Aug 21.

Abstract

BACKGROUND

Ménière's disease (MD) mainly refers to the endolymphatic hydrops in membranous labyrinth of the inner ear. Application of the mass spectrometry-based proteomics techniques has not been applied in the field of MD.

OBJECTIVES

To search for potential differential proteins to identify the disease biomarkers and reveal disease bioinformatics-related mechanisms through applying protein technology to analyze the expression changes of peripheral blood mononuclear cells (PBMCs) in sporadic MD patients.

MATERIAL AND METHODS

15 MD patients and 15 healthy individuals were enrolled. PBMCs from them were extracted, and their protein expression was identified and compared by LC-MS/MS and spectra analysis.

RESULTS

There was significant difference in protein expression between MD patients and the control group. GO and KEGG analysis showed that endocytosis was involved in MD patients. Western blot results of CHMP1A and MMP9 protein showed that the expression of CHMP1A was higher in the MD group than that in the control group, while MMP9 was down-regulated. Immunohistochemistry confirmed that CHMP1A and MMP9 were expressed in the endolymphatic sacs of MD patients and in the inner ear of adult mice.

CONCLUSIONS AND SIGNIFICANCE

Endocytosis may be involved in the pathogenesis of sporadic MD, furthermore CHMP1A, VPS4A, FCN3 and MMP9 could be considered as potential biomarkers.

摘要

背景

梅尼埃病(MD)主要是指内耳膜迷路的内淋巴积水。基于质谱的蛋白质组学技术尚未应用于 MD 领域。

目的

通过应用蛋白质组学技术分析散发性 MD 患者外周血单个核细胞(PBMC)的表达变化,寻找潜在的差异蛋白,以鉴定疾病生物标志物并揭示疾病生物信息学相关机制。

材料和方法

纳入 15 例 MD 患者和 15 例健康对照者。提取他们的 PBMC,通过 LC-MS/MS 和光谱分析鉴定和比较其蛋白表达。

结果

MD 患者和对照组之间的蛋白表达存在显著差异。GO 和 KEGG 分析显示内吞作用参与了 MD 患者的发病机制。CHMP1A 和 MMP9 蛋白的 Western blot 结果显示,MD 组 CHMP1A 的表达高于对照组,而 MMP9 则下调。免疫组化证实 CHMP1A 和 MMP9 在 MD 患者的内淋巴囊中以及成年小鼠的内耳中表达。

结论和意义

内吞作用可能参与散发性 MD 的发病机制,此外,CHMP1A、VPS4A、FCN3 和 MMP9 可被视为潜在的生物标志物。

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