Shitama Tomomi, Hayashi Hideyuki, Noge Sumiyo, Uchio Eiichi, Oshima Kenji, Haniu Hisao, Takemori Nobuaki, Komori Naoka, Matsumoto Hiroyuki
Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, P.O. Box 26901, Oklahoma City, OK73190, USA.
Proteomics Clin Appl. 2008 Sep;2(9):1265-1280. doi: 10.1002/prca.200800017.
Vitreous samples collected in retinopathic surgeries have diverse properties, making proteomics analysis difficult. We report a cluster analysis to evade this difficulty. Vitreous and subretinal fluid samples were collected from 60 patients during surgical operation of non-proliferative diabetic retinopathy, proliferative diabetic retinopathy, proliferative vitreoretinopathy, and rhegmatogenous retinal detachment. For controls we collected vitreous fluid from patients of idiopathic macular hole, epiretinal, and from a healthy postmortem donor. Proteins from these samples were subjected to quantitative proteomics using two-dimensional gel electrophoresis. We selected 105 proteins robustly expressed among ca 400 protein spots and subjected them to permutation test. By using permutation test analysis we observed unique variations in the expression of some of these proteins in vitreoretinal diseases when compared to the control and to each other: 1) the levels of inflammation-associate proteins such as AAT, APOA4, ALB, and TF were significantly higher in all four types of vitreoretinal diseases, and 2) each vitreoretinal disease elevates a unique set of proteins which can be interpreted based on the pathology of retinopathy. Our protocol will be effective for the study of protein expression in other types of clinical samples of diverse property.
视网膜病变手术中采集的玻璃体样本具有多种特性,这使得蛋白质组学分析变得困难。我们报告了一种聚类分析方法以规避这一难题。在非增殖性糖尿病视网膜病变、增殖性糖尿病视网膜病变、增殖性玻璃体视网膜病变和孔源性视网膜脱离的手术过程中,从60例患者身上采集了玻璃体和视网膜下液样本。作为对照,我们从特发性黄斑裂孔、视网膜前膜患者以及一名健康的尸体供体身上采集了玻璃体样本。使用二维凝胶电泳对这些样本中的蛋白质进行定量蛋白质组学分析。我们从大约400个蛋白点中选出了105个稳定表达的蛋白质,并对其进行排列检验。通过排列检验分析,我们观察到与对照组以及彼此相比,这些蛋白质中的一些在玻璃体视网膜疾病中的表达存在独特差异:1)在所有四种类型的玻璃体视网膜疾病中,炎症相关蛋白如α1抗胰蛋白酶(AAT)、载脂蛋白A4(APOA4)、白蛋白(ALB)和转铁蛋白(TF)的水平显著更高;2)每种玻璃体视网膜疾病都有一组独特的蛋白质升高,这可以根据视网膜病变的病理情况来解释。我们的方案对于研究其他具有不同特性的临床样本中的蛋白质表达将是有效的。