Objective To investigate the bioeffects of extremely low frequency （ELF） magnetic field （MF） （50 Hz, 400 μT） and magnetic nanoparticles （MNPs） via cytotoxicity and apoptosis assays on PC12 cells. Methods MNPs...Objective To investigate the bioeffects of extremely low frequency （ELF） magnetic field （MF） （50 Hz, 400 μT） and magnetic nanoparticles （MNPs） via cytotoxicity and apoptosis assays on PC12 cells. Methods MNPs modified by SiO2 （MNP-SiO2） were characterized by transmission electron microscopy （TEM）, dynamic light scattering and hysteresis loop measurement. PC12 cells were administrated with MNP-SiO2 with or without MF exposure for 48 h. Cytotoxicity and apoptosis were evaluated with MTI- assay and annexin V-FITC/PI staining, respectively. The morphology and uptake of MNP-SiO2 were determined by TEM. MF simulation was performed by Ansoft Maxwell based on the finite element method. Results MNP-SiO2 were identified as -20 nm （diameter） ferromagnetic particles. MNP-SiO2 reduced cell viability in a dose-dependent manner. MF also reduced cell viability with increasing concentrations of MNP-SiO2. MNP-SiO2 alone did not cause apoptosis in PC12 cells; instead, the proportion of apoptotic cells increased significantly under MF exposure and increasing doses of MNP-SiO2. MNP-SiO2 could be ingested and then cause a slight change in cell morphology. Conclusion Combined exposure of MF and MNP-SiO2 resulted in remarkable cytotoxicity and increased apoptosis in PC12 cells. The results suggested that MF exposure could strengthen the MF of MNPs, which may enhance the bioeffects of ELF MF.展开更多
基金supported by the State Key Development Program for Basic Research of China(2011CB503702)the Key Program of National Natural Science of China(51037006)
文摘Objective To investigate the bioeffects of extremely low frequency （ELF） magnetic field （MF） （50 Hz, 400 μT） and magnetic nanoparticles （MNPs） via cytotoxicity and apoptosis assays on PC12 cells. Methods MNPs modified by SiO2 （MNP-SiO2） were characterized by transmission electron microscopy （TEM）, dynamic light scattering and hysteresis loop measurement. PC12 cells were administrated with MNP-SiO2 with or without MF exposure for 48 h. Cytotoxicity and apoptosis were evaluated with MTI- assay and annexin V-FITC/PI staining, respectively. The morphology and uptake of MNP-SiO2 were determined by TEM. MF simulation was performed by Ansoft Maxwell based on the finite element method. Results MNP-SiO2 were identified as -20 nm （diameter） ferromagnetic particles. MNP-SiO2 reduced cell viability in a dose-dependent manner. MF also reduced cell viability with increasing concentrations of MNP-SiO2. MNP-SiO2 alone did not cause apoptosis in PC12 cells; instead, the proportion of apoptotic cells increased significantly under MF exposure and increasing doses of MNP-SiO2. MNP-SiO2 could be ingested and then cause a slight change in cell morphology. Conclusion Combined exposure of MF and MNP-SiO2 resulted in remarkable cytotoxicity and increased apoptosis in PC12 cells. The results suggested that MF exposure could strengthen the MF of MNPs, which may enhance the bioeffects of ELF MF.
