Analysis of HK-2 cells exposed to oxalate and calcium oxalate crystals: proteomic insights into the molecular mechanisms of renal injury and stone formation

被引:0
作者
Shushang Chen
Xiaofeng Gao
Yinghao Sun
Chuanliang Xu
Linhui Wang
Tie Zhou
机构
[1] Changhai Hospital of the Second Military Medical University,Department of Urology
[2] Fuzhou General Hospital,Department of Urology
[3] Nanjing Military Area Command of Chinese PLA,undefined
来源
Urological Research | 2010年 / 38卷
关键词
Renal epithelial cell; Oxalate; Calcium oxalate monohydrate; Nephrolithiasis; Proteomics;
D O I
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学科分类号
摘要
Exposure to high levels of oxalate and calcium oxalate monohydrate (COM) crystals is injurious to renal epithelial cells and triggers serial responses related to stone formation. Multiple molecules and proteins are involved in this process, but previous studies have generally been limited, without an overall understanding of protein expression alteration after oxalate and/or crystal exposure as well as its role in stone formation. We used proteomic analysis to reveal the changes in the proteome of HK-2 cells induced by oxalate and COM crystals, so as to provide candidate proteins involved in the molecular mechanisms concerning HK-2 cell injury and kidney stone formation. HK-2 cells were exposed to oxalate plus COM crystals at different concentrations in various samples. Cell viability was determined using a Cell Counting Kit-8 assay kit. For proteomic analysis, cells were exposed to oxalate (2 mM) and COM crystals (200 ug/ml) for 12 h. The proteins were separated by two-dimensional electrophoresis and the differentially expressed proteins were identified by liquid chromatography electrospray ionization tandem mass spectrometry (LC–ESI-MS/MS). Validation of protein expression was further performed by Western blot analysis. Oxalate and COM crystals showed concentration-dependent toxicity on HK-2 cells. A total of 12 differentially expressed proteins in HK-2 cells induced by oxalate and COM crystals were identified, which were involved in various aspects of cellular processes. Our study provides a platform for further studying the molecular mechanism of renal epithelial cell injury and kidney stone formation.
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页码:7 / 15
页数:8
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共 213 条
[21]  
Khan SR(2008)Proteomic analysis of altered proteins in distal renal tubular cells in response to calcium oxalate monohydrate crystal adhesion: implications for kidney stone disease Proteomics Clin Appl 2 1099-1109
[22]  
Verkoelen CF(2008)Altered proteins in MDCK renal tubular cells in response to calcium oxalate dihydrate crystal adhesion: a proteomics approach J Proteome Res 7 2889-2896
[23]  
Schepers MS(1995)Calcium oxalate crystallizing properties of polyanions elaborated by cultured renal proximal tubular cells Urol Res 23 103-110
[24]  
van Ballegooijen ES(2006)Expression profiling of crystal-induced injury in human kidney epithelial cells Nephron Physiol 103 53-62
[25]  
Bangma CH(1995)Adhesion of calcium oxalate monohydrate crystals to renal epithelial cells is inhibited by specific ions Am J Physiol 268 F604-F612
[26]  
Huang HS(2006)Reactive oxygen species-mediated calcium oxalate crystal-induced expression of MCP-1 in HK-2 cells Urol Res 34 26-36
[27]  
Ma MC(2007)Effect of urine fractionation on attachment of calcium oxalate crystals to renal epithelial cells: implications for studying renal calculogenesis Am J Physiol Renal Physiol 292 F1396-F1403
[28]  
Chen J(2005)Quantitative analysis of severe acute respiratory syndrome (SARS)-associated coronavirus-infected cells using proteomic approaches: implications for cellular responses to virus infection Mol Cell Proteomics 4 902-913
[29]  
Khan SR(2008)Developmental fate determination and marker discovery in hematopoietic stem cell biology using proteomic fingerprinting Mol Cell Proteomics 7 573-581
[30]  
Byer KJ(2006)Proteomic screening of glucose-responsive and glucose non-responsive MIN-6 beta cells reveals differential expression of proteins involved in protein folding, secretion and oxidative stress Proteomics 6 6578-6587