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首页> 外文期刊>BMC Urology >Comprehensive study of altered proteomic landscape in proximal renal tubular epithelial cells in response to calcium oxalate monohydrate crystals
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Comprehensive study of altered proteomic landscape in proximal renal tubular epithelial cells in response to calcium oxalate monohydrate crystals

机译:近端肾小管上皮细胞改变蛋白质组学横向响应含钙酸钙一水合物晶体的综合研究

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摘要

Calcium oxalate monohydrate (COM), the major crystalline composition of most kidney stones, induces inflammatory infiltration and injures in renal tubular cells. However, the mechanism of COM-induced toxic effects in renal tubular cells remain ambiguous. The present study aimed to investigate the potential changes in proteomic landscape of proximal renal tubular cells in response to the stimulation of COM crystals. Clinical kidney stone samples were collected and characterized by a stone component analyzer. Three COM-enriched samples were applied to treat human proximal tubular epithelial cells HK-2. The proteomic landscape of COM-crystal treated HK-2 cells was screened by TMT-labeled quantitative proteomics analysis. The differentially expressed proteins (DEPs) were identified by pair-wise analysis. Gene Ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis of DEPs were performed. Protein interaction networks were identified by STRING database. The data of TMT-labeled quantitative proteomic analysis showed that a total of 1141 proteins were differentially expressed in HK-2 cells, of which 699 were up-regulated and 442 were down-regulated. Functional characterization by KEGG, along with GO enrichments, suggests that the DEPs are mainly involved in cellular components and cellular processes, including regulation of actin cytoskeleton, tight junction and focal adhesion. 3 high-degree hub nodes, CFL1, ACTN and MYH9 were identified by STRING analysis. These results suggested that calcium oxalate crystal has a significant effect on protein expression profile in human proximal renal tubular epithelial cells.
机译:草酸钙一水合物(COM),大多数肾结石的主要晶体组合物,诱导肾小管细胞炎症浸润和损伤。然而,肾小管细胞中COM诱导的毒性作用的机制仍然存在含糊不清。本研究旨在探讨近端肾小管细胞蛋白质组学景观响应刺激COM晶体的潜在变化。收集临床肾脏石样品,并通过石材成分分析仪为特征。施用三个COM-富集样品以治疗人近端管状上皮细胞HK-2。通过TMT标记的定量蛋白质组学分析筛选COM晶体处理的HK-2细胞的蛋白质组学景观。通过对明智的分析鉴定差异表达的蛋白质(DEP)。基因本体(GO)分析(GO)分析和基因的京都百科全书(KEGG)DEPS的途径分析。通过字符串数据库识别蛋白质交互网络。 TMT标记的定量蛋白质组学分析的数据表明,在HK-2细胞中,总共1141个蛋白质在HK-2细胞中表达,其中699调节,442℃下调。 Kegg和GO富集的功能表征表明,DEPS主要参与细胞成分和细胞过程,包括肌动蛋白细胞骨架,紧密结和局灶性粘附的调节。 3通过字符串分析确定了3个高级中心节点,CFL1,ActN和MyH9。这些结果表明,草酸钙晶体对人近端肾小管上皮细胞中的蛋白质表达谱具有显着影响。

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