Integration of transcriptomic and metabolomic data reveals metabolic pathway alteration in mouse spermatogonia with the effect of copper exposure. (October 2020)

• Record Type: Journal Article
• Authors: Lin, Shuai; Qiao, Na; Chen, Hanming; Tang, Zhaoxin; Han, Qingyue; Mehmood, Khalid; Fazlani, Sarfaraz Ali; Hameed, Sajid; Li, Ying; Zhang, Hui
• Is Part Of: Chemosphere. Volume 256(2020)
• Publication Date: 2020-10
• Subjects: Copper -- Metabolomic -- Mouse spermatogonia -- Toxicity -- Transcriptomic; Pollution -- Periodicals; Pollution -- Physiological effect -- Periodicals; Environmental sciences -- Periodicals; Atmospheric chemistry -- Periodicals; 551.511
• DOI: 10.1016/j.chemosphere.2020.126974
• Languages: English
• ISSNs: 0045-6535

Abstract

Abstract: Copper is a widespread heavy metal in environment and has toxic effects when exposed. However, study of copper-induced male reproductive toxicity is still insufficient to report, and the underlying mechanisms are unknown. Keeping in view, RNA-Seq and metabolomic were performed to identify metabolic pathways that were distressed in mouse spermatogonia with the effect of copper sulfate, and the integrated analysis of the mechanism of copper administered GC-1 cells from metabolomic and transcriptomic data. Our results demonstrated that many genes and metabolites were regulated in the copper sulfate-treated cells. The differential metabolites analysis showed that 49 and 127 metabolites were significantly different in ESI+ and ESI- mode, respectively. Meanwhile, a total of 2813 genes were up-regulated and 2488 genes were down-regulated in the treatment groups compared to those in the control groups. Interestingly, ophthalmic acid and gamma glutamylleucine were markedly increased by copper treatment in two modes. By integrating with transcriptomic and metabolomic data, we revealed that 37 and 22 most related pathways were over-enriched in ESI+ and ESI- mode, respectively. Whereas, amino acid biosynthesis and metabolism play essential role in the potential relationship between DEGs and metabolites, which suggests that amino acid biosynthesis and metabolism may be the major metabolic pathways disturbed by copper in GC-1 cells. This study provides important clues and evidence for understanding the mechanisms responsible for copper-induced male spermatogenesis toxicity, and useful biomarkers indicative of copper exposure could be discovered from present study. Graphical abstract: Image 1 Highlights: Copper exposure resulted male infertility in mouse. Various genes expression and metabolic pathways change in GC-1 cells in copper toxicity. Amino acid biosynthesis is major pathway in GC-1 cells exposed to copper. This study provides new insight in understanding the crosstalk between copper toxicity and spermatogenesis.