Differentially Expressed Protein Profile of Renal Tubule Cell Stimulated by Elevated Uric Acid Using SILAC Coupled to LC-MS

细胞培养中氨基酸的稳定同位素标记 尿酸 细胞凋亡 阻抑素 细胞 细胞生长 信号转导 污渍 细胞生物学 化学 生物 蛋白质组学 分子生物学 癌症研究 生物化学 基因
作者
Quan Hong,Peng Xue,Shuwen Liu,Bo Fu,Yang Lv,Zhiyong Huang,Haixia Li,Xiangmei Chen,Di Wu
出处
期刊:Cellular Physiology and Biochemistry [Karger Publishers]
卷期号:27 (1): 91-98 被引量:27
标识
DOI:10.1159/000325209
摘要

Background/Aims: Hyperuricemia could lead to serious renal disease. It will advance our understanding of the mechanism of this disease to study the differentially expressed protein in renal tubular epithelial cells stimulated by elevated uric acid. Methods: We used SILAC coupled to LC-MS to study differentially expressed protein profile and to analysis the functional status of renal tubular epithelial cells stimulated by 600µM uric acid, and to investigate the potential biology function. The MS results were analyzed by online platform and further confirmed by western blotting. Results: 789 differentially expressed proteins were identified, of which 42 proteins and 49 proteins were related with cell proliferation and cell apoptosis, respectively. Pathway analysis showed that MAPK signaling pathway was a key pathway related to the function of these proteins. In addition, prohibitin-2 was identified to be related to renal cell transdifferentiation stimulated by elevated uric acid. Conclusion: This work provides an overview of protein expression changes in HK-2 cells treated with elevated uric acid and will contribute to further study of cell apoptosis and fibrosis in renal disease patients.

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