The interaction mechanism of nickel ions with L929 cells based on integrative analysis of proteomics and metabolomics data

被引:2
|
作者
Zhang, Yajing [1 ]
Huang, Yan [1 ]
Chen, Rong [1 ]
Chen, Shulin [1 ]
Lu, Xiaoying [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, 2 Si Pailou, Nanjing 210096, Peoples R China
基金
中国国家自然科学基金;
关键词
nickel ion (Ni2+); proteomics; metabolomics; protein-metabolite-metabolic pathway network; SILVER NANOPARTICLES; GLUTATHIONE-REDUCTASE; OXIDATIVE STRESS; GENE-EXPRESSION; MICE; CYTOTOXICITY; METABOLISM; TOXICITY; PROLINE; DEATH;
D O I
10.1093/rb/rbac040
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The aim of this article was to study the toxicity mechanism of nickel ions (Ni2+) on L929 cells by combining proteomics and metabolomics. First, iTRAQ-based proteomics and LC/MS metabolomics analyses were used to determine the protein and metabolite expression profiles in L929 cells after treatment with 100 mu M Ni2+ for 12, 24 and 48 h. A total of 177, 2191 and 2109 proteins and 40, 60 and 74 metabolites were found to be differentially expressed. Then, the metabolic pathways in which both differentially expressed proteins and metabolites were involved were identified, and three pathways with proteins and metabolites showing upstream and downstream relationships were affected at all three time points. Furthermore, the protein-metabolite-metabolic pathway network was constructed, and two important metabolic pathways involving 4 metabolites and 17 proteins were identified. Finally, the functions of the important screened metabolic pathways, metabolites and proteins were investigated and experimentally verified. Ni2+ mainly affected the expression of upstream proteins in the glutathione metabolic pathway and the arginine and proline metabolic pathway, which further regulated the synthesis of downstream metabolites, reduced the antioxidant capacity of cells, increased the level of superoxide anions and the ratio of GSSG to GSH, led to oxidative stress, affected energy metabolism and induced apoptosis.
引用
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页数:12
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