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持续低氧对海马神经元凋亡及蛋白表达影响 被引量:1

Apoptosis and expressions of c-jun,c-fos in rat hippocampal cells in vitro with continuous hypoxia
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摘要 目的观察持续低氧致体外培养SD乳大鼠海马神经元细胞凋亡及c-jun、c-fos的表达情况。方法海马神经元原代细胞培养,取培养10 d的海马神经元,置于90%N2、5%O2、5%CO2混合气体培养箱中培养2,6,12,24h后,Hoechst 33258染色观察神经元细胞凋亡情况,并用蛋白印迹法检测c-jun、c-fos蛋白表达水平。结果随缺氧时间延长,凋亡细胞所占比例由(23.79±3.43)%上升至(74.36±5.58)%;c-jun、c-fos蛋白在缺氧2 h时表达增高,6 h时达高峰,之后逐渐降低,24 h时仍略高于正常对照。结论持续低氧可引起体外培养海马神经元c-jun、c-fos蛋白表达升高,这可能与神经细胞凋亡以及保护机制有关。 Objective To observe the cell apoptosis and the expressions of c-jun,c-fos in neonatal SD rat hippocampal cells with continuous hypoxia in vitro.Methods After ten-days primary culture,the hippocampal cells were exposed to 90% N2,5% O2,5% CO2 for 2,6,12,and 24 hours.The apoptosis of the cells was identified by Hoechst 33258 staining and the expressions of c-jun,c-fos was analyzed with western-blot.Results With the extension period of hypoxia,the number of apoptotic cells was significantly increased from 23.79 ± 3.43% to 74.36 ± 5.58%.Western-blot assay showed the ex-pressions of c-jun,c-fos increased at 2 hr,and reached the highest at 6 hr and then gradually decreased,but were still higher than those of the control at 24 hr.Conclusion Continuous hypoxia can induce the expression of c-jun,c-fos in hippocampal cells in vitro,which might be related to the cell apoptosis and the neuron protective mechanism.
出处 《中国公共卫生》 CAS CSCD 北大核心 2010年第11期1397-1398,共2页 Chinese Journal of Public Health
基金 国家自然科学基金(30671779)
关键词 持续低氧 海马神经元 凋亡 C-JUN C-FOS continuous hypoxia hippocampus neuron apoptosis c-jun c-fos
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  • 1颚征 主编.组织培养技术.第2版[M].北京:人民卫生出版社,1993.63.
  • 2Zhang Y,Zhou L,& Miller CA (1998).A splicing variant of a death domain protein that is regulated by a mitogen-activated kinase is a substrate for c-Jun N-terminal kinase in the human central nervous system.Proc.Natl.Acad.Sci.U.S.A.,95,2586-2591.
  • 3Ferrer I,Planas AM.Signaling of cell death and cell survival following focal cerebral ischemia:life and death struggle in the penumbra.J Neu-ropathol Exp Neurol,2003,62:329-339.
  • 4Perry DK.Ceramide and apoptosis.Biochem Soc Trans,1999,27:399-404.
  • 5Kabuyama Y,Homma MK,Sekimata M,Homma Y.Wavelength-specific activation of MAP kinase family proteins by monochromatic UV irradiation.Photochem Photobiol 2001;73:147-152.
  • 6Adler V,Polotskaya A,Kim J,Dolan L,Davis R,Pincus M,Ronai Z.Dose rate and mode of exposure are key factors in JNK activation by UV irradiation.Carcinogenesis 1996;17:2073-2076.
  • 7Iordanov MS,Magun BE.Different mechanisms of c-Jun NH(2)-terminal kinase-1 (JNK1) activation by ultraviolet-B radiation and by oxidative stressors.J Biol Chem 1999;274:25801-25806.
  • 8Chen YH,Wang X,Templeton D,Davis RJ,Tan TH.The role of c-Jun N-terminal kinase (JNK) in apoptosis induced by ultraviolet C and gamma radiation.Duration of JNK activation may determine cell death and proliferation.J Biol Chem 1996;271:31929-31936.
  • 9Tournier C,Hess P,Yang DD,XuJ,Turner TK,Nimnual A,Bar-Sagi D,Jones SN,Flavell RA,Davis RJ.Requirement of JNK for stress-induced activation of the cytochrome c-mediated death pathway.Science 2000;288:870-874.
  • 10Wang X,Martindale JL,Liu Y,Holbrook NJ.The cellular response to oxidative stress:Influences of mitogenactivated protein kinase signalling pathways on cell survival.Biochem J 1998;333:291-300.

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