Chromium [Cr(VI)] Exposure Causes Cytotoxicity of Human Bronchial Epithelial Cells (16-HBE) and Proteomic Alterations

被引:4
|
作者
Xia, Bo [1 ,2 ]
Yuan, Jiao [1 ]
Pang, Li [3 ]
He, Kaiwu [2 ]
机构
[1] Hunan Agr Univ, Coll Food Sci & Technol, East Renmin Rd, Changsha 410128, Hunan, Peoples R China
[2] Shenzhen Ctr Dis Control & Prevent, Key Lab Modern Toxicol Shenzhen, Shenzhen 518055, Guangdong, Peoples R China
[3] Hunan Agr Univ, Coll Hort, East Renmin Rd, Changsha, Peoples R China
关键词
hexavalent chromium; human bronchial epithelial cells; proteomics; cytotoxicity; INDUCED DNA-DAMAGE; HEXAVALENT CHROMIUM; KAPPA-B; EXPRESSION; CHROMATE; NICKEL; CANCER; TRANSFORMATION; METHYLATION; ACTIVATION;
D O I
10.1177/10915818221078277
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hexavalent chromium [Cr(VI)] is a common industrial pollutant, and exposure may cause toxic effects in multiple organ systems and carcinogenesis, including lung cancer. However, the toxic effect of Cr(VI) on the respiratory system is poorly understood. In the present study, it was demonstrated that Cr(VI) exposure significantly decreased the viability of human bronchial epithelial cells (16-HBE) in a dose-dependent manner. Flow cytometry demonstrated that Cr(VI) enhanced the transition of 16-HBE cells from G(1) to S phase and arrested S-phase progression. Reverse transcription-quantitative polymerase chain reaction analysis revealed a significant alteration in the expression of apoptosis-associated genes in Cr(VI)-treated 16-HBE cells. In addition, using two-dimensional fluorescence differential gel electrophoresis with mass spectrometry, 15 differentially expressed proteins (1 upregulated and 14 downregulated) were identified in 16-HBE cells with Cr(VI) treatment compared with controls. Functional classification revealed that these differentially expressed proteins were involved in apoptosis, cytoskeletal structure, and energy metabolism. In conclusion, these data suggested that Cr(VI) caused toxic effects in bronchial epithelial cells and the mechanisms may involve the abnormal expression of apoptosis-associated proteins, cytoskeletal proteins, and energy metabolism-associated proteins.
引用
收藏
页码:225 / 233
页数:9
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