Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.
J Proteomics. 2012 Jun 6;75(10):2950-9. doi: 10.1016/j.jprot.2011.12.006. Epub 2011 Dec 20.
Diabetic retinopathy (DR) can cause irreversible blindness and is the severest microvascular complication in the eyes of patients with diabetic mellitus (DM). The identification of susceptibility factors contributing to development of DR is helpful for identifying predisposed patients and improving treatment efficacy. Although proteomics analysis is useful for identifying protein markers related to diseases, it has never been used to explore DR-associated susceptibility factors in the aqueous humor (AH). To better understand the pathophysiology of DR and to identify DR-associated risk factors, a gel-based proteomics analysis was performed to compare AH protein profiles of DM patients with and without development of DR. MALDI-TOF MS was then performed to identify protein spots that were differentially expressed between the two groups and western blot analysis was used to validate the expressional change of protein demonstrated by proteomics. Our proteomics and bioinformatics analysis identified 11 proteins differentially expressed between DR and control groups. These proteins are linked to biological networks associated with nutrition transport, microstructure reorganization, angiogenesis, anti-oxidation, and neuroprotection. The data may provide potential AH biomarkers and susceptibility factors for predicting DR development, and provide an insight into the underlying pathophysiological mechanisms of DR. This article is part of a Special Issue entitled: Proteomics: The clinical link.
糖尿病性视网膜病变(DR)可导致不可逆性失明,是糖尿病患者眼中最严重的微血管并发症。鉴定导致 DR 发生的易患因素有助于识别易患患者并提高治疗效果。尽管蛋白质组学分析有助于鉴定与疾病相关的蛋白质标记物,但它从未用于探索房水中与 DR 相关的易患因素。为了更好地了解 DR 的病理生理学并鉴定 DR 相关的危险因素,进行了基于凝胶的蛋白质组学分析,以比较患有和不患有 DR 的糖尿病患者的房水蛋白质图谱。然后进行 MALDI-TOF MS 以鉴定两组之间差异表达的蛋白质斑点,并使用 Western blot 分析验证蛋白质组学显示的蛋白质表达变化。我们的蛋白质组学和生物信息学分析鉴定了 DR 组和对照组之间差异表达的 11 种蛋白质。这些蛋白质与与营养运输、微观结构重组、血管生成、抗氧化和神经保护相关的生物网络有关。这些数据可能为预测 DR 发展提供潜在的房水生物标志物和易患因素,并深入了解 DR 的潜在病理生理机制。本文是一个题为“蛋白质组学:临床联系”的特刊的一部分。