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DOI 10.1016/j.chemosphere.2019.125629

Медицинская библиотека · Chemosphere · 2019

A metabolomics study: CdTe/ZnS quantum dots induce polarization in mice microglia.

He Keyu, Liang Xue, Wei Tingting, Liu Na, Wang Yan, Zou Linyue, Bai Changcun, Yao Ying, Wu Tianshu, Kong Lu, Zhang Ting, Xue Yuying, Tang Meng

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Аннотация

In this study, a metabolomic analysis was used to reveal the neurotoxicity of the CdTe/ZnS QDs via microglia polarization. A gas chromatography-mass spectrometer (GC-MS) was applied to uncover the metabonomic changes in microglia (BV-2 cell line) after exposure to 1.25 μM CdTe/ZnS QDs. 11 annotated metabolic pathways (KEGG database) were significantly changed in all exposed groups (3 h, 6 h, 12 h), 3 of them were related to glucose metabolism. The results of the Seahorse XFe96 Analyzer indicated that the CdTe/ZnS QDs increased the glycolysis level of microglia by 86% and inhibited the aerobic respiration level by 54% in a non-hypoxic environment. In vivo study, 3 h after the injection of CdTe/ZnS QDs (2.5 mM) through the tail vein in mice, the concentration of the CdTe/ZnS QDs in hippocampus reached the peak (1.25 μM). The polarization level of microglia (Iba-1 immunofluorescence) increased 2.7 times. In vitro study, the levels of the extracellular TNF-α, IL-1β and NO of BV-2 cells were all increased significantly after a 6 h or 12 h exposure. According to the results of the Cell Counting Kit-8, after a 6 h or 12 h exposure to the CdTe/ZnS QDs, the exposed microglia could significantly decrease the number of neurons (HT-22 cell line). This study proved that CdTe/ZnS QDs could polarize microglia in the brain and cause secondary inflammatory damage to neurons. There are potential risks in the application of the CdTe/ZnS QDs in brain tissue imaging.

Для цитирования: He Keyu, Liang Xue, Wei Tingting, Liu Na, Wang Yan, Zou Linyue, Bai Changcun, Yao Ying, Wu Tianshu, Kong Lu, Zhang Ting, Xue Yuying, Tang Meng. A metabolomics study: CdTe/ZnS quantum dots induce polarization in mice microglia.. Chemosphere. 2019. DOI: 10.1016/j.chemosphere.2019.125629.

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