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蛋白质组学揭示圆锥角膜进展延迟的机制:一项关于两次光活化交联治疗后角膜的研究。

Proteomics Reveals Mechanisms of Delayed Keratoconus Progression: A Study of Corneas Following Two Light-Activated Crosslinking Treatments.

作者信息

Vogels Demi H J, Brekelmans Jurriaan, Mohren Ronny, Vos Naomi R N, Brandis Alexander, Marcovich Arie L, Cillero-Pastor Berta, Scherz Avigdor, LaPointe Vanessa L S, Dickman Mor M

机构信息

University Eye Clinic Maastricht, Maastricht University Medical Center, Maastricht, the Netherlands.

Department of Cell Biology-Inspired Tissue Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, the Netherlands.

出版信息

Invest Ophthalmol Vis Sci. 2025 Jan 2;66(1):64. doi: 10.1167/iovs.66.1.64.

Abstract

PURPOSE

This study aims to elucidate on changes in biological pathways in rabbit corneas induced by two methods of light-activated corneal stiffening: topical application of riboflavin with dextran (RF-D) or WST11 with dextran (WST-D) followed by ultraviolet A (UVA) or near-infrared (NIR) illumination, respectively.

METHODS

Rabbit corneas were mechanically de-epithelialized, then left untreated (N = 3) or treated with either RF-D/UVA (N = 3) or WST-D/NIR (N = 3). After one week, quantitative proteomics was performed on untreated, RF-D/UVA- and WST-D/NIR-treated corneas. Pathway enrichment analysis was performed to identify the biological processes associated with the treatments. To identify the abundance and spatial distribution of lipids in the untreated, WST-D/NIR- and RF-D/UVA-treated corneal stroma, lipid mass spectrometry imaging was performed together with hematoxylin and eosin staining.

RESULTS

Between RF-D/UVA- and WST-D/NIR-treated corneas, 37 and 39 proteins, respectively, were differentially expressed compared to untreated corneas (P < 0.05). Pathway enrichment analysis showed the effect of RF-D/UVA treatment on cell metabolism and terminal differentiation of keratocytes, while WST-D/NIR modified extracellular matrix regulation and the mitogen-activated protein kinase signaling cascade. When comparing the RF-D/UVA and WST-D/NIR treatment, 74 proteins were differentially expressed, affecting cellular metabolism and respiration, complement activation, the activation of matrix metalloproteinases, and lipoprotein metabolism. The lipid profile for the RF-D/UVA- and WST-D/NIR-treated stromas were similar, whereas differences were observed comparing both treatments to untreated corneal stroma.

CONCLUSIONS

Proteomics indicated a metabolic shift from oxidative phosphorylation to glycolysis and hypoxia after RF-D/UVA treatment. In contrast, WST-D/NIR stiffening maintained normal respiration and involved extracellular matrix remodeling.

摘要

目的

本研究旨在阐明两种光激活角膜硬化方法诱导兔角膜生物途径的变化:分别用含葡聚糖的核黄素(RF-D)或含葡聚糖的WST11(WST-D)局部应用,随后分别进行紫外线A(UVA)或近红外(NIR)照射。

方法

兔角膜经机械去上皮处理,然后不进行处理(N = 3)或用RF-D/UVA(N = 3)或WST-D/NIR(N = 3)处理。一周后,对未处理、RF-D/UVA处理和WST-D/NIR处理的角膜进行定量蛋白质组学分析。进行通路富集分析以确定与处理相关的生物学过程。为了确定未处理、WST-D/NIR处理和RF-D/UVA处理的角膜基质中脂质的丰度和空间分布,同时进行脂质质谱成像和苏木精-伊红染色。

结果

与未处理的角膜相比,RF-D/UVA处理和WST-D/NIR处理的角膜分别有37种和39种蛋白质差异表达(P < 0.05)。通路富集分析表明,RF-D/UVA处理对角细胞的细胞代谢和终末分化有影响,而WST-D/NIR改变了细胞外基质调节和丝裂原活化蛋白激酶信号级联反应。比较RF-D/UVA和WST-D/NIR处理时,有74种蛋白质差异表达,影响细胞代谢和呼吸、补体激活、基质金属蛋白酶的激活以及脂蛋白代谢。RF-D/UVA处理和WST-D/NIR处理的基质脂质谱相似,而将两种处理与未处理的角膜基质相比则观察到差异。

结论

蛋白质组学表明,RF-D/UVA处理后代谢从氧化磷酸化转变为糖酵解和缺氧。相比之下,WST-D/NIR硬化维持正常呼吸并涉及细胞外基质重塑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/567f/11781325/0ae7d035aaea/iovs-66-1-64-f001.jpg

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