期刊文献+

低氧诱导因子1α在大鼠脊髓损伤中的表达 被引量:5

Expression of hypoxia inducible factor-1α in spinal cord injury
原文传递
导出
摘要 目的 了解低氧诱导因子 1α(hypoxiainduciblefactor- 1α ,HIF - 1α)在实验性脊髓损伤中的表达规律并探讨其在脊髓损伤中的作用。 方法 通过逆转录聚合酶链式反应 (RT -PR)、原位杂交和免疫组化方法 ,分别从mRNA和蛋白水平研究HIF - 1α在脊髓损伤后不同时段的表达情况。结果 HIF - 1α的mRNA和蛋白在损伤脊髓中的各种细胞类型中广泛表达 ,而且表达较正常脊髓明显增高 (P <0 .0 5 ) ,其中蛋白表达高峰 (伤后 1d)较mRNA表达高峰 (伤后 3d)提前。 结论 脊髓损伤中存在缺血缺氧损害 ,缺氧环境可通过诱导转录和增强蛋白稳定性来增加HIF - 1α蛋白量 ,这可能与HIF - 1α的下游基因激活和脊髓组织细胞耐受缺氧环境有关。 Objective To explore the expression pattern and effects of hypoxia inducible factor-1α (HIF-1α) in experimental spinal cord injury. Methods The expression of HIF-1α at various time was detected at levels of mRNA and protein by using methods of reverse transcription-polymerase chain reaction (RT-PCR),in situ hybridization (ISH) and immunohistochemistry. Results HIF-1α expressed more significantly at levels of mRNA and protein in all kinds of cells in the injured spinal cord than in the normal spinal cord (P<0.05). The protein expression of HIF-1α reached climax at the first day after operation, earlier than the mRNA expression (at the third day after operation). Conclusions Hypoxia-ischemia damage exists in spinal cord injury. Hypoxia circumstance can increase protein content by inducing transcription and reinforcing stability of HIF-1α protein, as may relate to the activation of HIF-1α downstream genes and the cell tolerance of spinal cord tissue to hypoxia circumstance.
出处 《中华创伤杂志》 CAS CSCD 北大核心 2003年第9期544-547,共4页 Chinese Journal of Trauma
基金 国家自然科学基金资助项目 ( 3 9970 75 5 )
关键词 脊髓损伤 低氧诱导因子1Α 逆转录聚合酶链式反应 原位杂交 免疫组织化学 Hypoxia inducible factor Spinal cord injury Ischemia hypoxia
  • 相关文献

参考文献17

  • 1Semenza GL, Wang GL. A nuclear factor induced by hypoxia via denovo protein synthesis binds to the human erythropoietin gene enhancer at a site required for transcriptional activation. Mol Cell Biol,1992, 12:5447-5454.
  • 2Forsythe JA, Jiang BH, Iyer NV, et al. Activation of vascular endothelial growth factor gene transcription by hypoxia - inducible factor 1. Mol Cell Biol, 1996, 16:4604-4613.
  • 3Wang GL, Semenza GL. Purification and characterization of hypoxiainducible factor 1. J Biol Chem, 1995, 270:1230-1237.
  • 4Wang GL, Semenza GL. Desferrioxamine induces erythropoietin gene expression and hypoxia-inducible factor 1 DNA-binding activity:implications for models of hypoxia signal transduction. Blood, 1993,82, 3610-3615.
  • 5Kimura H, Weisz A, Kurashima Y, et al. Hypoxia response element of the human vascular endothelial growth factor gene mediates transcriptional regulation by nitric oxide: control of hypoxia-inducible factor-1 activity by nitric oxide. Blood, 2000, 95:189-197.
  • 6Hartsfield CL, Alam J, Choi AM. Differential signaling pathways of HO-1 gene expression in pulmonary and systemic vascular cells. Am J Physiol, 1999, 277:L1133-L1141.
  • 7Jung F, Palmer LA, Zhou N, et al. Hypoxic regulation of inducible nitric oxide synthase via hypoxia inducible factor-1 in cardiac myocytes. Circ Res, 2000, 86:319-325.
  • 8Ebert BL, Firth JD, Ratcliffe PJ. Hypoxia and mitochondrial inhibitors regulate expression of glucose transporter-1 via distinct Cisacting sequences. J Biol Chem, 1995, 270:29083-29089.
  • 9Bianchi L, Tacchini L, Cairo G. HIF-1-mediated activation of transferrin receptor gene transcription by iron chelation. Nucleic Acids Res, 1999, 27:4223- 4227.
  • 10Semenza GL, Jiang BH, Leung SW, et al. Hypoxia response elements in the aldolase A, enolase 1, and lactate dehydrogenase A gene promoters contain essential binding sites for hypoxia-inducible factor 1. J Biol Chem, 1996, 271:32529-32537.

同被引文献83

  • 1曹晓建.一氧化氮在脊髓损伤中的作用[J].国外医学(神经病学.神经外科学分册),1996,23(4):175-178. 被引量:11
  • 2董瑞剑,赵仁亮.缺氧诱导因子-1与脑缺血耐受[J].国际脑血管病杂志,2006,14(5):377-380. 被引量:4
  • 3顾天爵.生物化学(第3版)[M].北京:人民卫生出版社,1994.163-167.
  • 4Vincent KA,Shyu KG,Luo Y,et al.Angiogenesis is induced in a rabbit model of hindlimb ischemia by naked DNA encoding an HIF-1alpha/VP16 hybrid transcription factor.Circulation,2000,102:2255-2261.
  • 5Shyu KG,Wang MT,Wang BW,et al.Intramyocardial injection of naked DNA encoding HIF-1alpha/VP16 hybrid to enhance angiogenesis in an acute myocardial infarction model in the rat.Cardiovasc Res,2002,54:576-583.
  • 6Li J,Post M,Volk R,et al.PR39,a peptide regulator of angiogenesis.Nat Med,2000,6:49-55.
  • 7Willam C,Masson N,Tian YM,et al.Peptide blockade of HIFalpha degradation modulates cellular metabolism and angiogenesis.Proc Natl Acad Sci USA,2002,99:10423-10428.
  • 8Nwogu JI,Geenen D,Bean M,et al.Inhibition of collagen synthesis with prolyl 4-hydroxylase inhibitor improves left ventricular function and alters the pattern of left ventricular dilatation after myocardial infarction.Circulation,2001,104:2216-2221.
  • 9Huang LE,Bunn HF.Hypoxia-inducible factor and its biomedical relevance.J Biol Chem,2003,278:19575-19578.
  • 10Hirota K.Hypoxia-inducible factor 1,a master transcription factor of cellular hypoxic gene expression.J Anesth,2002,16:150-159.

引证文献5

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部