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首页> 外文期刊>American Journal of Nephrology >Protein Expression Profile of Human Renal Mesangial Cells under High Glucose.
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Protein Expression Profile of Human Renal Mesangial Cells under High Glucose.

机译:高糖下人肾小球膜细胞的蛋白质表达谱。

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摘要

Background: To understand the spectrum of proteins affected by diabetic nephropathy and to characterize the molecular functions and biological processes they control, the protein expression profile of human renal mesangial cells (HMCs) under high glucose was analyzed. Methods: HMCs were divided into a high glucose-cultured group (30 mmol/l) and a normal glucose-cultured group (5 mmol/l). The total proteins of the two groups were separated and analyzed by two-dimensional difference gel electrophoresis (DIGE). Spots that were differentially expressed were picked and digested with trypsin and subjected to MALDI-TOF MS for protein identification. Results: 147 protein spots whose expression levels were significantly increased or decreased more than 1.5-fold in HMCs under high glucose culture were identified. 32 proteins were identified by peptide mass fingerprinting. The protein spots of phosphatidylethanolamine-binding protein 1, granulysin, ATP synthase, H(+) transporter, mitochondrial F0 complex and subunit F2 were observed only in the high glucose group. The expression of 24 proteins was upregulated by high glucose, including eosinophil cationic protein and others. The expression of 5 proteins was downregulated by high glucose, including proteasome beta6 subunit precursor, among others. Conclusion: 32 protein expressions of human glomerular mesangial cells were regulated by high glucose. In-depth analysis of these differentially expressed proteins' function and crosstalk is expected to provide an experimental basis for clarifying the pathogenesis of diabetic nephropathy.
机译:背景:为了了解受糖尿病肾病影响的蛋白质谱并表征其控制的分子功能和生物学过程,分析了高葡萄糖条件下人肾小球膜细胞(HMC)的蛋白质表达谱。方法:将HMC分为高糖培养组(30 mmol / l)和正常糖培养组(5 mmol / l)。分离两组的总蛋白,并通过二维差异凝胶电泳(DIGE)进行分析。挑选差异表达的斑点,并用胰蛋白酶消化,然后用MALDI-TOF MS进行蛋白质鉴定。结果:在高糖培养条件下,鉴定出147个蛋白斑点,其表达水平在HMC中显着升高或降低了1.5倍以上。通过肽质谱指纹图谱鉴定了32种蛋白质。仅在高葡萄糖组中观察到磷脂酰乙醇胺结合蛋白1,颗粒溶素,ATP合酶,H(+)转运蛋白,线粒体F0复合体和F2亚基的蛋白斑点。高糖可上调24种蛋白的表达,其中包括嗜酸性粒细胞阳离子蛋白等。 5种蛋白质的表达被高葡萄糖下调,其中包括蛋白酶体beta6亚基前体。结论:高糖调节人肾小球系膜细胞的32种蛋白表达。这些差异表达蛋白的功能和串扰的深入分析有望为阐明糖尿病性肾病的发病机理提供实验基础。

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