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马关节软骨外植体骨关节炎模型:代谢组学和蛋白质组学研究。

Equine Cartilage Explant Osteoarthritis Model: A Metabolomics and Proteomics Study.

机构信息

Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool L7 8TX, U.K.

NMR Metabolomics Facility, Technology Directorate & Department of Biochemistry & Systems Biology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 7ZB, U.K.

出版信息

J Proteome Res. 2020 Sep 4;19(9):3652-3667. doi: 10.1021/acs.jproteome.0c00143. Epub 2020 Aug 6.

Abstract

Osteoarthritis is an age-related degenerative musculoskeletal disease characterized by loss of articular cartilage, synovitis, and subchondral bone sclerosis. Osteoarthritis pathogenesis is yet to be fully elucidated with no osteoarthritis-specific biomarkers in clinical use. equine cartilage explants ( = 5) were incubated in tumor necrosis factor-α (TNF-α)/interleukin-1β (IL-1β)-supplemented culture media for 8 days, with the media removed and replaced at 2, 5, and 8 days. Acetonitrile metabolite extractions of 8 day cartilage explants and media samples at all time points underwent one-dimensional (1D) H nuclear magnetic resonance metabolomic analysis, with media samples also undergoing mass spectrometry proteomic analysis. Within the cartilage, glucose and lysine were elevated following TNF-α/IL-1β treatment, while adenosine, alanine, betaine, creatine, myo-inositol, and uridine decreased. Within the culture media, 4, 4, and 6 differentially abundant metabolites and 154, 138, and 72 differentially abundant proteins were identified at 1-2, 3-5, and 6-8 days, respectively, including reduced alanine and increased isoleucine, enolase 1, vimentin, and lamin A/C following treatment. Nine potential novel osteoarthritis neopeptides were elevated in the treated media. Implicated pathways were dominated by those involved in cellular movement. Our innovative study has provided insightful information on early osteoarthritis pathogenesis, enabling potential translation for clinical markers and possible new therapeutic targets.

摘要

骨关节炎是一种与年龄相关的退行性肌肉骨骼疾病,其特征是关节软骨丧失、滑膜炎和软骨下骨硬化。骨关节炎的发病机制尚未完全阐明,临床上也没有骨关节炎特异性生物标志物。将 5 个马软骨外植体置于肿瘤坏死因子-α(TNF-α)/白细胞介素-1β(IL-1β)补充的培养基中孵育 8 天,每隔 2、5 和 8 天更换培养基。对第 8 天软骨外植体和所有时间点的培养基样本进行乙腈代谢物提取,进行一维(1D)H 核磁共振代谢组学分析,同时对培养基样本进行质谱蛋白质组学分析。在软骨中,TNF-α/IL-1β 处理后葡萄糖和赖氨酸升高,而腺苷、丙氨酸、甜菜碱、肌酸、肌醇和尿苷降低。在培养基中,分别在 1-2、3-5 和 6-8 天,鉴定出 4、4 和 6 种差异丰度代谢物和 154、138 和 72 种差异丰度蛋白,包括处理后丙氨酸减少和异亮氨酸增加、烯醇酶 1、波形蛋白和核纤层蛋白 A/C。在处理过的培养基中,有 9 种潜在的新型骨关节炎新生肽升高。涉及的途径主要是与细胞运动相关的途径。我们的创新性研究为早期骨关节炎发病机制提供了有见地的信息,为临床标志物和可能的新治疗靶点的潜在转化提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c1/7476031/ccd45fa60432/pr0c00143_0002.jpg

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