期刊文献+

缺氧对神经细胞缺氧诱导因子-1αmRNA表达的影响 被引量:1

The expression and clinical significance of HIF-1α mRNA in neurons under hypoxia
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摘要 目的 揭示在缺氧状态下神经细胞缺氧诱导因子 - 1α(HIF - 1α)mRNA表达的时空规律。方法 对分离的新生SD大鼠大脑皮质神经细胞分别进行常规和缺氧培养 ,采用定量逆转录多聚酶链反应 (RT -PCR)检测神经细胞在不同缺氧时间HIF - 1αmRNA的表达。结果 神经细胞在常氧下HIF - 1αmRNA有极低的表达 ,在缺氧30min时表达量显著上升 ,6 0min达到高峰 ,90min后逐渐下降。与对照组比较 ,各缺氧组HIF - 1αmRNA的表达均有显著性差异 (P <0 .0 1)。结论 神经细胞在缺氧早期HIF - 1αmRNA表达有短暂。 Objective To explore the law of the expression of HIF-1α mRNA in neurons under hypoxia and its clinical implication. Methods The cortical neurons,prepared from neonatal SD rats, were cultured in normoxic and hypoxic condition respectively.Quantitative reverse transcription-polymerase chain reaction (RT-PCR) was employed to examine the expression of HIF-1α mRNA in neurons. Results In normoxic condition the expression of HIF-1α mRNA in neurons was at a very low level.While under hypoxia, the level of expression increased rapidly and transiently, with the maximal expression at 90 min after hypoxia. Compared with the normoxic group, the expression of HIF-1α mRNA in the hypoxic groups all had a significant difference (P<0.01). Conclusion These results demonstrate the expression of HIF-1α increases rapidly and transiently under hypoxia.
出处 《徐州医学院学报》 CAS 2001年第2期87-88,共2页 Acta Academiae Medicinae Xuzhou
基金 江苏省科委应用基础课题 !(DJ995 0 1)
关键词 缺氧 诱导因子-1Α 逆转录聚合酶链反应 神经细胞 缺氧 MRNA hypoxia inducible factor-1α RT-PCR neuron hypoxia
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参考文献4

  • 1Semenza GL.Expression of hypoxia- inducible factor 1: mechanisms and consequence[].Biochemical Pharmacology.2000
  • 2Ruscher K,Isaev N.Induction of hypoxia inducible factor 1 by oxygen glucose deprivation is attenuated by hypoxic preconditioning in rat cultured neurons[].Neuroscience Letters.1998
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同被引文献9

  • 1Suzuki H,Tomida A,Tsuruo T.Dephosphorylated hypoxia-inducible factor 1alpha as a mediator of p53-dependent apoptosis during hypoxia.Oncogene 2001 ;20(41):5779-88.
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  • 3Semenza GL,Wang GL.A nuclear factor inducd by hypoxia via de novo protein synthesis binds to the human erythropoietin gene enhancer at a site required for transcriptional activation.Moll Cell Biol 1992; 12(12):5447-54.
  • 4Caro J.Hypoxia regulation of gene transcription.High Alt Med Biol 2001 ;2(2):145-54.
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  • 6Semenza GL.Expression of hypoxia-inducible factor 1:mechanisms and consequence.Biochem Pharmacol 2000; 59(1):47-53.
  • 7徐少骏,鲍卫汉,陈东明,王琦.增殖瘢痕成纤维细胞接触后增殖及生物合成特性对异常瘢痕形成的机理[J].中华整形外科杂志,2002,18(2):86-88. 被引量:19
  • 8秦泽莲.增生性瘢痕异常增生的启动因素[J].中华整形外科杂志,2003,19(2):135-137. 被引量:23
  • 9李高峰,罗成群,刘浔阳,贺全勇,李萍,徐阳成.烧伤后瘢痕内缺氧环境的变化[J].中国烧伤创疡杂志,2004,16(1):4-8. 被引量:8

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