Zhang Yajing, Huang Yan, Chen Rong, Chen Shulin, Lü Xiaoying
State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, 2# Si Pailou, Nanjing 210096, China.
Regen Biomater. 2022 Jun 23;9:rbac040. doi: 10.1093/rb/rbac040. eCollection 2022.
The aim of this article was to study the toxicity mechanism of nickel ions (Ni) 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 μM Ni 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. Ni 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.
本文旨在通过蛋白质组学和代谢组学相结合的方法研究镍离子(Ni)对L929细胞的毒性机制。首先,采用基于iTRAQ的蛋白质组学和LC/MS代谢组学分析方法,测定100μM Ni处理12、24和48小时后L929细胞中的蛋白质和代谢物表达谱。共发现177、2191和2109种蛋白质以及40、60和74种代谢物差异表达。然后,鉴定了差异表达的蛋白质和代谢物均参与的代谢途径,在所有三个时间点均有三条蛋白质和代谢物呈现上下游关系的途径受到影响。此外,构建了蛋白质-代谢物-代谢途径网络,鉴定出两条涉及4种代谢物和17种蛋白质的重要代谢途径。最后,对筛选出的重要代谢途径、代谢物和蛋白质的功能进行了研究并通过实验验证。Ni主要影响谷胱甘肽代谢途径和精氨酸与脯氨酸代谢途径中上游蛋白质的表达,进而调节下游代谢物的合成,降低细胞的抗氧化能力,增加超氧阴离子水平以及GSSG与GSH的比值,导致氧化应激,影响能量代谢并诱导细胞凋亡。