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阿柏西普干预实验性中心性视网膜静脉阻塞的蛋白质组分析。

Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion.

机构信息

Department of Ophthalmology, Odense University Hospital, 5000 Odense C, Denmark.

Department of Ophthalmology, Aalborg University Hospital, 9000 Aalborg, Denmark.

出版信息

Molecules. 2022 May 24;27(11):3360. doi: 10.3390/molecules27113360.

Abstract

Aflibercept is a frequently used inhibitor of vascular endothelial growth factor (VEGF) in the treatment of macular edema following central retinal vein occlusion (CRVO). Retinal proteome changes following aflibercept intervention in CRVO remain largely unstudied. Studying proteomic changes of aflibercept intervention may generate a better understanding of mechanisms of action and uncover aspects related to the safety profile. In 10 Danish Landrace pigs, CRVO was induced in both eyes with an argon laser. Right eyes were treated with intravitreal aflibercept while left control eyes received isotonic saline water. Retinal samples were collected 15 days after induced CRVO. Proteomic analysis by tandem mass tag-based mass spectrometry identified a total of 21 proteins that were changed in content following aflibercept intervention. In retinas treated with aflibercept, high levels of aflibercept components were reached, including the VEGF receptor-1 and VEGF receptor-2 domains. Fold changes in the additional proteins ranged between 0.70 and 1.19. Aflibercept intervention resulted in a downregulation of pigment epithelium-derived factor (PEDF) (fold change = 0.84) and endoplasmin (fold change = 0.91). The changes were slight and could thereby not be confirmed with less precise immunohistochemistry and Western blotting. Our data suggest that aflibercept had a narrow mechanism of action in the CRVO model. This may be an important observation in cases when macular edema secondary to CRVO is resistant to aflibercept intervention.

摘要

阿柏西普是一种常用于治疗视网膜中央静脉阻塞(CRVO)后黄斑水肿的血管内皮生长因子(VEGF)抑制剂。CRVO 中阿柏西普干预后的视网膜蛋白质组变化在很大程度上仍未得到研究。研究阿柏西普干预的蛋白质组变化可能会更好地了解作用机制,并揭示与安全性相关的方面。在 10 只丹麦兰德瑞斯猪中,双眼均用氩激光诱导 CRVO。右眼用玻璃体内注射阿柏西普治疗,左眼用等渗盐水作为对照。在诱导 CRVO 后 15 天收集视网膜样本。通过串联质量标签质谱的蛋白质组分析共鉴定出 21 种在阿柏西普干预后含量发生变化的蛋白质。在接受阿柏西普治疗的视网膜中,达到了高水平的阿柏西普成分,包括 VEGF 受体-1 和 VEGF 受体-2 结构域。其他蛋白质的倍数变化在 0.70 到 1.19 之间。阿柏西普干预导致色素上皮衍生因子(PEDF)(倍数变化=0.84)和内质网蛋白(fold change = 0.91)下调。这些变化很轻微,因此用不太精确的免疫组织化学和 Western blot 无法证实。我们的数据表明,阿柏西普在 CRVO 模型中具有狭窄的作用机制。这在 CRVO 引起的黄斑水肿对阿柏西普干预耐药的情况下可能是一个重要的观察结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4af3/9182497/542730760b0e/molecules-27-03360-g001.jpg

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