Graphene quantum dots disturbed the energy homeostasis by influencing lipid metabolism of macrophages.

Center for Clinical Pharmacy, Cancer Center, Department of Pharmacy, Zhejiang Provincial People's Hospital (Affiliated People's Hospital, Hangzhou Medical College), Hangzhou, Zhejiang 310014, China. Biomedical Analysis Center, Army Medical University, Chongqing 400038, China. Department of Pharmacy, No. 958 Hospital of PLA, Southwest Hospital, Army Military Medical University, Chongqing 400020, China. Electronic address: laixiaodan0926@sina.com. Institute of Rocket Force Medicine, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical University, Chongqing 400038, China. Electronic address: 956873053@qq.com. Biomedical Analysis Center, Army Medical University, Chongqing 400038, China. Electronic address: lf112.2004@163.com. Biomedical Analysis Center, Army Medical University, Chongqing 400038, China. Electronic address: huangyi@tmmu.edu.cn.

Toxicology. 2023;:153389
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Abstract

To investigate the potential factors of graphene quantum dots (GQDs), the assessment impact on the innate immune system is one of the most important. As the innate immune cell, macrophages possess phagocytosis activity and affect immunomodulation. Higher oxygen consumption rates (OCR) are used to gain insight into GQDs' effects on macrophages. Metabolomics profiling also revealed that GQDs exposure provoked an increase in phosphoglycerides, sphingolipids, and oxidized lipids in macrophages. The molecular pathways disrupted by GQDs were associated with lipid and energy metabolisms. Metabolite flux analysis was used to evaluate changes in the lipid metabolism of macrophages exposed to 100 µg mL-1 GQDs for 24 and 48 h. A combination of 13C-flux analysis and metabolomics revealed the regulation of lipid biosynthesis influenced the balance of energy metabolism. Integrated proteomics and metabolomics analyses showed that nicotinic acid adenine dinucleotide and coenzyme Q10 were significantly increased under GQDs treatment, alongside upregulated protein activity (e.g., Cox5b and Cd36). The experimental evidences were expected to be provided in this study to reveal the potential harmful effect from exposure to GQDs.