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Proteomic Analysis of Various Rat Ocular Tissues after Ischemia–Reperfusion Injury and Possible Relevance to Acute Glaucoma

机译:缺血再灌注损伤后大鼠各种眼组织的蛋白质组学分析及其与急性青光眼的可能相关性

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摘要

Glaucoma is a group of eye diseases that can cause vision loss and optical nerve damage. To investigate the protein expression alterations in various intraocular tissues (i.e., the cornea, conjunctiva, uvea, retina, and sclera) during ischemia–reperfusion (IR) injury, this study performed a proteomic analysis to qualitatively investigate such alterations resulting from acute glaucoma. The IR injury model combined with the proteomic analysis approach of two-dimensional difference gel electrophoresis (2D-DIGE) and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was used to monitor the protein expression alterations in two groups of specimens (an IR injury group and a control group). The analysis results revealed 221 unique differentially expressed proteins of a total of 1481 proteins in the cornea between the two groups. In addition, 97 of 1206 conjunctival proteins, 90 of 1354 uveal proteins, 61 of 1180 scleral proteins, and 37 of 1204 retinal proteins were differentially expressed. These findings imply that different ocular tissues have different tolerances against IR injury. To sum up, this study utilized the acute glaucoma model combined with 2D-DIGE and MALDI-TOF MS to investigate the IR injury affected protein expression on various ocular tissues, and based on the ratio of protein expression alterations, the alterations in the ocular tissues were in the following order: the cornea, conjunctiva, uvea, sclera, and retina.
机译:青光眼是一组可能导致视力丧失和视神经损伤的眼部疾病。为了研究缺血再灌注(IR)损伤期间各种眼内组织(即角膜,结膜,葡萄膜,视网膜和巩膜)的蛋白质表达变化,本研究进行了蛋白质组学分析,定性研究了由急性青光眼引起的这种变化。将红外损伤模型与蛋白质组学分析方法(二维差异凝胶电泳(2D-DIGE)和基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS))结合使用,以监测蛋白质表达两组标本(IR损伤组和对照组)有变化。分析结果显示两组之间角膜中共有148种蛋白质的221种独特的差异表达蛋白质。另外,差异表达了1206个结膜蛋白中的97个,1354个葡萄膜蛋白中的90个,1180个巩膜蛋白中的61个以及1204个视网膜蛋白中的37个。这些发现暗示不同的眼组织对IR损伤具有不同的耐受性。综上所述,本研究利用急性青光眼模型结合2D-DIGE和MALDI-TOF MS来研究IR损伤影响的各种眼组织蛋白质表达,并基于蛋白质表达变化的比率,眼组织的变化按以下顺序排列:角膜,结膜,葡萄膜,巩膜和视网膜。

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