期刊文献+

自噬/溶酶体途径在多巴胺神经元变性中的作用 被引量:1

下载PDF
导出
摘要 目的:探索自噬/溶酶体途径是否参与了帕金森病(Parkinson’s disease,PD)病人及PD动物模型黑质多巴胺神经元损伤机制。方法:取PD病人中脑切片,用免疫荧光双标记观察黑质细胞溶酶体蛋白酶B和L(Cathepsin B and L)的表达;用立体定位技术将6-羟基多巴(6-OHDA)8μg/4μl注射到大鼠右侧黑质致密部(Substantia nigra pars compaeta.SNpc。)制作PD大鼠模型,DNA凝胶电泳及TUNEL法检测DA神经元的变性,免疫组化法检测多巴胺神经元cathepsin B及eathepsin L、溶酶体相关膜糖蛋白-1(LAMP-1)的表达,
出处 《中国药理通讯》 2005年第3期32-33,共2页
  • 相关文献

同被引文献15

  • 1陈生弟.帕金森病治疗指南[J].中华神经科杂志,2006,39(6):409-412. 被引量:102
  • 2Levine B,Kroemer G.Autophagy in the pathogenesis of disease[J].Cell,2008,132(1):27-42.
  • 3Pan T,Kondo S.The role of autophagy-lysosome pathway in neurodegeneration associated with Parkinson's disease[J].Brain,2008,131(Pt 8):1 969-1 978.
  • 4Zhang K,Calabrese P,Nordborg M,et al.Haplotype block structure and its applications to association studies:power and study designs[J].Am J Hum Genet,2002,71(6):1 386-1 394.
  • 5Vaineta Valeikiene,Jelena Ceremnych,Diana Mieliauskaite,et al.The prevalence of Parkinson's disease among Vilnius inhabitants[J].Cent Eur J Med,2008,3(2):195-198.
  • 6Rubinsztein DC.The roles of intracellular protein-degradation pathways in neurodegeneration[J].Nature,2006,443:780-786.
  • 7Korolchuk VI,Mansilla A,Menzies FM,et al.Autophagy inhibition compromises degradation of ubiquitin-proteasome pathway substrates[J].Mol Cell,2009,33(4):517-527.
  • 8Bredesen DE.Programmed cell death mechanisms in neurological disease[J].Curr Mol Med,2008,8:173-186.
  • 9Herrera VL,Decano JL,Steffen M,et al.Autophagy:insights from DEspR-deficiency and haploinsufficiency[J].Autophagy,2009,5(2):259-262.
  • 10Mizushima N,Yamamoto A,Hatano M,et al.Dissection of autophagosome formation using Apg5-deficient mouse embryonic stem cells[J].J Cell Biol,2001,152:657-667.

引证文献1

二级引证文献3

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