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电磁辐射对N9小胶质细胞STAT3核转位以及磷酸化水平的影响

Effect of electromagnetic irradiation induced STAT3 DNA binding and phosphorylation in N9 microglial cells
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摘要 目的研究STAT3信号分子是否参与电磁辐射诱导的小胶质细胞活化。方法Western-blot检测小胶质细胞STAT3蛋白质表达及磷酸化表达变化,凝胶迁移率实验(Electrophoretic Mobility Shift Assay,EMSA)检测小胶质细胞STAT3的DNA结合活性的变化。结果电磁辐射后小胶质细胞STAT3磷酸化增强,STAT3核转位与DNA结合活性在辐照后6-24h增加,并以12h最为明显。结论STAT3信号分子参与了电磁辐射诱导的小胶质细胞活化过程。 Objective To investigate the possible participation of STAT3 signaling molecule and activation of microglia after electromagnetic irradiation. Methods Phosphorylation of STAT3 was tested using western blotting. STAT3 DNA binding activity was detected by EMSA. Results After electromagnetic irradiation, the phosphorylation of STAT3 was detected rapidly post microwave exposure. A significant increase of STAT3 DNA-binding ability was noted from 6b to 24h after exposure, especially at 12h. Conclusion The STAT3 signaling molecule may participate in the activation of microglia induced by electromagnetic irradiation.
出处 《中国国境卫生检疫杂志》 CAS 2011年第2期73-76,共4页 Chinese Journal of Frontier Health and Quarantine
基金 国家自然科学基金项目(30470418)
关键词 电磁辐射 N9小胶质细胞 STAT3信号分子 磷酸化 Electromagnetic irradiation N9 microglial cell STAT3 Signaling molecule Phosphorylation
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  • 1Schwab BL, Guerini D, Didszun C, et al. Cleavage of plasma membrane calcium pumps by caspases: a link between apoptosis and necrosis. Cell Death Differ, 2002, 9: 818-831.
  • 2Wang B, Lai H. Acute exposure to pulsed 2450-MHz microwaves affects water-maze performance of rats. Bioelectromagnetics, 2000, 21 :52-56.
  • 3Dias N, Nicolau A, Carvallco GS, et al. Miniatarization and application of the MTT assay to evaluate metabolic activity of protozoa in the presence of toxicants. Basic Microbiol, 1999, 39: 103-108.
  • 4Koopman G, Reutelingsperger CP, Kuijten GA, et al. Annexin V for flow cytometric detection of phosphatidylserine expression on B cells undergoing apoptosis. Blood, 1994, 84: 1415-1420.
  • 5Grondahl T, Langmoen IA. Confocal laser scanning microscopy used tomonitor intracellular Ca^2+ changes in hippocampal CA1 neurons during energy deprivation. Brain Res, 1998,785: 58-65.
  • 6Jang YK, Park JJ, Lee MC, et al. Retinoic acid-mediated induction of neurons and glial cells from human umbilical cord-derived hematopoietic stem cells. J Neurosci Res, 2004, 75: 573-584.
  • 7Carreno-Muller E, Herrera A J, de Pablos RM, et al. Thrombin induces in vivo degeneration of nigral dopaminergic neurons along with the activation of microglia[J]. J Neurochem, 2003, 84(5): 1201-1214.
  • 8Choi SH, Joe EH, Kim SU, et al. Thrombin-induced microglial activation produces degeneration of nigral dopaminergic neurons in vivo [J]. J Neurosci, 2003, 23(13) :5877-5886.
  • 9Choi SH, Lee DY, Ryu JK, et al. Thrombin induces nigral dopaminergic neurodegeneration in vivo by altering expression of death-related proteins [ J ]. Neurobiol Dis, 2003, 14(2): 181-193.
  • 10Herrera A J, Tomas-Camardiel M, Venero J L, et al. Inflammatory process as a determinant factor for the degeneration of substantia nigra dopaminergic neurons [J].J Neural Transm, 2005, 112(1): 111-119.

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