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Proteomic analysis of human proximal tubular cells exposed to high glucose concentrations

机译:暴露于高葡萄糖浓度的人类近端肾小管细胞的蛋白质组学分析

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Hyperglycemia is a major key factor in the pathogenesis of microvascular complications of diabetes, including diabetic nephropathy (DN). Most studies to date have focused on the glomerular abnormalities found in DN. However, nephromegaly in the early stages of diabetes and the correlation of tubulointerstitial pathology rather than glomerular pathology with declining renal function in DN suggests the involvement of the tubulointerstitium. The etiology of the tubulointerstitial pathology in DN, however, is not fully understood. In this study, to understand the DN pathways, we constructed an initial 2-DE reference map for primitively cultured human proximal tubule (HK-2) cell in the presence of 5 mM and 25 mM glucose, which correspond to blood glucose concentrations during the normal and hyperglycemia conditions, respectively. Differentially expressed HK-2 cell cellular proteins at the high glucose concentration were identified via ESI-Q-TOF MS/MS and confirmed by Western blotting; enolase 1 (up-regulated) and lactate dehydrogenase (down-regulated). The regulation of these proteins will help in understanding DN mechanism through the glycolysis metabolic pathways in high glucose stimulated HK-2 cells.
机译:高血糖症是糖尿病微血管并发症(包括糖尿病肾病(DN))发病机理中的主要关键因素。迄今为止,大多数研究都集中在DN中发现的肾小球异常。然而,糖尿病早期的肾肿大和肾小管间质病变而不是肾小球病理与DN肾功能下降的相关性提示肾小管间质受累。但是,DN的肾小管间质病变的病因尚未完全了解。在这项研究中,为了了解DN途径,我们为存在5 mM和25 mM葡萄糖的情况下原始培养的人近端肾小管(HK-2)细胞构建了一个初始2-DE参考图,这对应于正常和高血糖情况。通过ESI-Q-TOF MS / MS鉴定高葡萄糖浓度下差异表达的HK-2细胞细胞蛋白,并通过Western印迹进行确认;烯醇酶1(上调)和乳酸脱氢酶(下调)。这些蛋白质的调节将通过高糖刺激的HK-2细胞中的糖酵解代谢途径帮助理解DN机制。

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