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细胞内和细胞外非靶向代谢组学揭示了急性铀暴露对HK-2细胞的影响。

Intracellular and extracellular untargeted metabolomics reveal the effect of acute uranium exposure in HK-2 cells.

作者信息

Cheng Xuedan, Chu Jian, Zhang Liandong, Suo Zhirong, Tang Wei

机构信息

School of Materials Science and Engineering, Southwest University of Science and Technology, Mianyang 621010, China; Center for Medical Radiation Biology, 903 Hospital, Institute of Materials, China Academy of Engineering Physics, Mianyang 621907, China.

Center for Medical Radiation Biology, 903 Hospital, Institute of Materials, China Academy of Engineering Physics, Mianyang 621907, China.

出版信息

Toxicology. 2022 May 15;473:153196. doi: 10.1016/j.tox.2022.153196. Epub 2022 May 4.

Abstract

Uranium exposure poses a serious threat to the health of occupational populations and the public. Although metabolomics is a promising research approach to study the toxicological mechanisms of uranium exposure, in vitro studies using human cells are scarce. Applying cultured cell metabolomics, we exhaustively analyzed the intracellular and extracellular differential metabolites upon uranium exposure and characterized the possible biological effects of uranium exposure on human kidney cells. Uranium exposure significantly induced disturbance in the amino acid biosynthesis and linoleic acid metabolism of the cells. Cells exposed to uranium produce excessive amounts of arachidonic acid, which has the potential to cause oxidative stress and damage cells. The results provide new evidence for an oxidative stress mechanism of uranium-induced renal cell injury. Cell metabolomics has proven to be a useful diagnostic tool to study the molecular mechanisms of uranium poisoning.

摘要

铀暴露对职业人群和公众的健康构成严重威胁。尽管代谢组学是研究铀暴露毒理学机制的一种有前景的研究方法,但使用人类细胞的体外研究却很匮乏。应用培养细胞代谢组学,我们详尽分析了铀暴露后细胞内和细胞外的差异代谢物,并表征了铀暴露对人肾细胞可能产生的生物学效应。铀暴露显著诱导了细胞氨基酸生物合成和亚油酸代谢的紊乱。暴露于铀的细胞会产生过量的花生四烯酸,这有可能导致氧化应激并损伤细胞。这些结果为铀诱导肾细胞损伤的氧化应激机制提供了新证据。细胞代谢组学已被证明是研究铀中毒分子机制的一种有用诊断工具。

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