Protective Effects of Cerium Oxide Nanoparticles on MC3T3-E1 Osteoblastic Cells Exposed to X-Ray Irradiation

被引:27
作者
Wang, Cuifen [1 ,2 ]
Blough, Eric [1 ,2 ]
Dai, Xiaoniu [3 ]
Olajide, Omolola [4 ]
Driscoll, Henry [4 ,5 ]
Leidy, John W. [4 ,5 ]
July, Mose [4 ]
Triest, William E. [5 ]
Wu, Miaozong [1 ,2 ,4 ]
机构
[1] Marshall Univ, Ctr Diagnost Nanosyst, Huntington, WV USA
[2] Marshall Univ, Sch Pharm, Huntington, WV USA
[3] Southeast Univ, Sch Med, Nanjing, Jiangsu, Peoples R China
[4] Marshall Univ, Dept Internal Med, Joan C Edwards Sch Med, Huntington, WV USA
[5] Huntington Vet Affairs Med Ctr, Huntington, WV USA
关键词
X-ray irradiation; Cerium oxide nanoparticles; MC3T3-E1; cells; Oxidative stress; Micronucleus; Mineralization; IONIZING-RADIATION; GAMMA-RADIATION; IN-VITRO; ALKALINE-PHOSPHATASE; LIPID-PEROXIDATION; HUMAN-LYMPHOCYTES; DNA-DAMAGE; P38; MAPK; BONE; APOPTOSIS;
D O I
10.1159/000443092
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: Exposure to ionizing radiation can result in bone damage, including decreased osteocyte number and suppressed osteoblastic activity. However, molecular mechanisms remain to be elucidated, and effective prevention strategies are still limited. This study was to investigate whether cerium oxide nanoparticles (CeO2 NP) can protect MC3T3-E1 osteoblast-like cells from damaging effects of X-ray irradiation, and to study the underpinning mechanism(s) Methods: MC3T3-El, a osteoblast-like cell line, was exposed to X-ray irradiation and treated with different concentration of CeO2 nanoparticles. The micronucleus frequency was counted under a fluorescence microscope. Cell viability was evaluated using MTT assay. The effects of irradiation and CeO2 nanoparticles on alkaline phosphatase activity and MC3T3-E1 mineralization were further assayed. Results: We found that the ratio of micronuclei to binuclei was dose -dependently increased with X-ray irradiation (from 2 to 6 Gy), but diminished with the increased concentration of CeO2 NP treatment (from 50 to 100 nM). Exposure to X-rays (6 Gy) decreased cell viability, differentiation and the mineralization, but CeO2 NP treatment (100 nM) attenuated the deteriorative effects of irradiation. Both intracellular reactive oxygen species (ROS) production and extracellular H2O2 concentration were increased after X-ray irradiation, but reduced following CeO2 NP treatment. Similar to irradiation, exposure to H2O2 (10 p M) elevated the frequency of micronuclei and diminished cell viability and mineralization, while these changes were ameliorated following CeO2 NP treatment. Conclusions: Taken together, our findings suggest that CeO2 nanoparticles exhibit astonishing protective effects on irradiation induced osteoradionecrosis in MC3T3-E1 cells, and the protective effects appear to be mediated, at least partially, by reducing oxidative stress. (C) 2016 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:1510 / 1519
页数:10
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