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Identification of proteins associated with clinical and pathological features of proliferative diabetic retinopathy in vitreous and fibrovascular membranes

机译:鉴定与玻璃体和纤维血管膜增生性糖尿病视网膜病变的临床和病理特征相关的蛋白质

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摘要

To identify the protein profiles in vitreous associated with retinal fibrosis, angiogenesis, and neurite formation in epiretinal fibrovascular membranes (FVMs) in patients with proliferative diabetic retinopathy (PDR). Vitreous samples of 5 non-diabetic control patients with vitreous debris and 7 patients with PDR membranes were screened for 507 preselected proteins using the semi-quantitative RayBio® L-series 507 antibody array. From this array, 60 proteins were selected for a custom quantitative antibody array (Raybiotech, Human Quantibody® array), analyzing 7 control patients, 8 PDR patients with FVMs, and 5 PDR patients without FVMs. Additionally, mRNA levels of proteins of interest were measured in 10 PDR membranes and 11 idiopathic membranes and in retinal tissues and cells to identify possible sources of protein production. Of the 507 proteins screened, 21 were found to be significantly elevated in PDR patients, including neurogenic and angiogenic factors such as neuregulin 1 (NRG1), nerve growth factor receptor (NGFR), placental growth factor (PlGF) and platelet derived growth factor (PDGF). Angiopoietin-2 (Ang2) concentrations were strongly correlated to the degree of fibrosis and the presence of FVMs in patients with PDR. Protein correlation analysis showed PDGF to be extensively co-regulated with other proteins, including thrombospondin-1 and Ang2. mRNA levels of glial-derived and brain/derived neurotrophic factor (GDNF and BDNF) were elevated in PDR membranes. These results were validated in a second study of 52 vitreous samples of 32 PDR patients and 20 control patients. This exploratory study reveals protein networks that potentially contribute to neurite outgrowth, angiogenesis and fibrosis in the formation of fibrovascular membranes in PDR. We identified a possible role of Ang2 in fibrosis and the formation of FVMs, and of the neurotrophic factors NRG1, PDGF and GDNF in neurite growth that occurs in all FVMs in PDR
机译:若要确定与增殖性糖尿病性视网膜病(PDR)患者视网膜纤维化,血管生成和视网膜神经纤维膜(FVMs)中的神经突形成相关的玻璃体中的蛋白质谱。使用半定量RayBio®L系列507抗体阵列,对5例非糖尿病性玻璃体碎片对照患者和7例PDR膜患者的玻璃体样品进行了507种预选蛋白的筛选。从该阵列中,选择60种蛋白质用于定制的定量抗体阵列(Raybiotech,HumanQuantibody®阵列),分析7例对照患者,8例具有FVM的PDR患者和5例无FVM的PDR患者。此外,在10个PDR膜和11个特发性膜以及视网膜组织和细胞中测量了目标蛋白的mRNA水平,以确定可能的蛋白生产来源。在筛选的507种蛋白质中,发现21种在PDR患者中显着升高,包括神经源性和血管生成性因子,例如神经调节蛋白1(NRG1),神经生长因子受体(NGFR),胎盘生长因子(PlGF)和血小板衍生生长因子( PDGF)。 PDR患者中血管生成素2(Ang2)的浓度与纤维化程度和FVM的存在密切相关。蛋白质相关性分析显示PDGF与其他蛋白(包括血小板反应蛋白1和Ang2)广泛共调节。 PDR膜中神经胶质和脑/神经营养因子(GDNF和BDNF)的mRNA水平升高。这些结果在32位PDR患者和20位对照患者的52个玻璃体样品的第二项研究中得到了验证。这项探索性研究揭示了可能在PDR中形成神经血管膜,血管生成和纤维化的蛋白质网络。我们确定了Ang2在纤维化和FVM形成以及神经营养因子NRG1,PDGF和GDNF在PDR中所有FVM中发生的神经突生长中的可能作用。

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