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蛋白质组学分析患有分支视网膜静脉阻塞引起的黄斑水肿患者的房水。

Proteomic analysis of aqueous humor from patients with branch retinal vein occlusion-induced macular edema.

机构信息

Department of Ophthalmology, Nanjing Children's Hospital Affiliated to Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.

出版信息

Int J Mol Med. 2013 Dec;32(6):1421-34. doi: 10.3892/ijmm.2013.1509. Epub 2013 Sep 25.

Abstract

The mechanisms responsible for macular edema with branch retinal vein occlusion (BRVO) remain to be elucidated. It is known that the expression profile of certain proteins in the aqueous humor (AH) changes in some diseases. Accordingly, determining the expression of these AH proteins may aid in the understanding of their potential role in this pathogenesis. The aim of this study was to identify the possible mechanisms involved in the development of BRVO-induced macular edema. A proteomic analysis of the AH composition in the eyes of patients with BRVO was performed and compared with that in the eyes of patients with cataract (non-BRVO; controls). AH from 6 patients with macular edema due to BRVO and 6 patients with cataract (non-BRVO) was collected. A proteomic approach which included 2‑dimensional electrophoresis (2‑DE) coupled with mass spectrometry (MS) and bioinformatics analysis were used to identify AH proteins with altered expression in patients with macular edema due to BRVO compared with the controls. An enzyme‑linked immunosorbent assay was used to validate the proteomic results. The total protein concentration in the AH of patients with BRVO-induced macular edema was significantly greater than that of the controls. In the patients with BRVO, a total of 56 protein spots were significantly altered on the 2D gels. A total of 49 protein spots were identified by MS; many of these proteins have been implicated in angiogenesis, oxidative stress and collagen synthesis. In conclusion, the protein composition in AH differed significantly between the patients with BRVO and the controls. The identified proteins may be potential biomarkers for the development of macular edema due to BRVO and may play a role in the mechanisms responsible for it.

摘要

导致分支视网膜静脉阻塞(BRVO)黄斑水肿的机制仍有待阐明。已知在某些疾病中,房水中某些蛋白质的表达谱会发生变化。因此,确定这些房水蛋白的表达情况可能有助于了解它们在发病机制中的潜在作用。本研究旨在确定可能参与 BRVO 引起的黄斑水肿发展的机制。对 BRVO 患者房水中的蛋白质组成进行了蛋白质组学分析,并与白内障(非 BRVO;对照组)患者的房水中的蛋白质组成进行了比较。收集了 6 例 BRVO 引起的黄斑水肿患者和 6 例白内障(非 BRVO)患者的房水。采用二维电泳(2-DE)结合质谱(MS)和生物信息学分析的蛋白质组学方法,鉴定出与对照组相比,BRVO 患者黄斑水肿房水中表达改变的 AH 蛋白。酶联免疫吸附试验用于验证蛋白质组学结果。BRVO 引起的黄斑水肿患者房水中的总蛋白浓度明显高于对照组。在 BRVO 患者中,2D 凝胶上有 56 个蛋白点明显改变。通过 MS 共鉴定出 49 个蛋白点;其中许多蛋白质与血管生成、氧化应激和胶原合成有关。总之,BRVO 患者和对照组的房水蛋白组成有显著差异。所鉴定的蛋白质可能是 BRVO 引起的黄斑水肿发展的潜在生物标志物,并可能在其发病机制中发挥作用。

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