| Literature DB >> 33222613 |
Tongwang Luo1,2,3,4, Qi Yu1,2,3, Wenxuan Dong1,2,3, Zhonggui Gong1,2,3, Yun Tan1,2,3, Wenjing Liu1,2,3, Hui Zou1,2,3, Jianhong Gu1,2,3, Yan Yuan1,2,3, Jianchun Bian1,2,3, Chunyan Shao4, Jiaqiao Zhu1,2,3, Zongping Liu1,2,3.
Abstract
Heavy metal pollution is a problem that cannot be ignored. Due to the prevalence of cadmium in the environment and its harmful effects on humans, cadmium pollution has become a research hotspot recently. The mechanism of cadmium-induced toxicity has also drawn much attention and most studies have been conducted using whole cells, but the toxicological mechanism of cadmium remains unclear. In this study, we aimed to obtain NRK-52E cells at different growth stages by various methods and analyze the differences in cadmium toxicity. The results show that the cadmium sensitivity of cells in each phase was different and the late apoptotic rate was increased significantly after 5 µM Cd treatment. In addition, cadmium easily induces apoptosis of G0- and S-phase cells, as well as necrosis of S- and M-phase cells, but has no significant effect on G1-phase cells. Overall, we first explored the differences in the effects of cadmium on NRK-52E cells at various growth phases. Besides, the findings of this study might provide a theoretical basis for further exploration of the toxicological mechanism of cadmium.Abbreviations Cd: cadmium; CDK: cyclin-dependent kinases; DAPI 2-(4-amidinophenyl)-1H-indole-6-carboxamidine; TBST: Tris-buffered saline with Tween-20; PI: propidium iodide; DMEM: Dulbecco's Modified Eagle Medium; BCA: bicinchoninic acid.Entities:
Keywords: Cell cycle synchronization; NRK-52E cells; apoptosis; cadmium; necrosis
Year: 2020 PMID: 33222613 PMCID: PMC7751682 DOI: 10.1080/15384101.2020.1848065
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534