期刊文献+

磷酸化Rb蛋白在正常成年大鼠与脑缺血大鼠神经元内的表达变化

Expression and subcellular localization of phospho-Rb in neurons of adult rats and rats subjected to focal cerebral ischemia
暂未订购
导出
摘要 目的观察正常成年大鼠与局灶性脑缺血大鼠神经元内磷酸化Rb蛋白(p-Rb)的表达及变化特点。方法应用免疫荧光组织化学染色方法观察成年大鼠不同脑区神经元内p-Rb表达特点,比较大鼠大脑中动脉闭塞(MCAO)后不同时间点(12h、1d、3d、7d)缺血半暗带内神经元p-Rb的变化特点。结果成年大鼠神经元内p-Rb主要在细胞核内表达;与对照组相比,MCAO再灌注后各时间点p-Rb免疫反应性均增强;再灌注1d,缺血半暗带内部分神经元p-Rb表达由细胞核转移到细胞浆。结论成熟神经元内p-Rb在细胞核内表达可能对于维持神经元的有丝分裂后状态有一定作用,当其发生核浆转移提示神经元细胞周期调控机制紊乱,可能再进入细胞周期。 Objective To investigate the expression and changes of subcellular localization of phospho-Rb in neu- rons of adult rats and rats subjected to transient focal cerebral isehemia. Methods Immunofluorescence staining was used to detect the expression and subcellular localization of phospho-Rb in neurons of adult rats in different cerebral regions and in the penumbra zone at 12h, 1 d, 3d and 7d after middle cerebral artery occlusion (MCAO)/reperfusion. Results Phos- pho-Rb was mainly located in the nuclei under normal conditions. Compared with sham-operated controls, increased phos- pho-Rb immunoreactivity was seen at each time point after MCAO/reperfusion. One day after reperfusion,it was showed that subcellular localization of phospho-Rb translocated from the nucleus to the cytoplasm in many neurons in the penumbra zone. Conclusion Located in the nuclei of mature neurons, phospho-Rh palys a potential role in maintaining neuronal post- mitotic quiescence. Cytoplasmic translocation of phospho-Rb from nucleus occurs in impaired neurons, suggesting that these neurons attempt to reenter cell cycle mediated by dysregulation of the cell cycle machinery after focal cerebral ischemia.
出处 《中风与神经疾病杂志》 CAS CSCD 北大核心 2012年第6期484-486,共3页 Journal of Apoplexy and Nervous Diseases
基金 国家自然科学基金重点项目(No.81030021) 武汉大学青年教师自主创新项目(No.111089)
关键词 局灶性脑缺血 神经元 细胞周期 磷酸化Rb Focal cerebral ischemia Neuron Cell cycle Phospho-Rb
  • 相关文献

参考文献12

  • 1Schmetsdorf S, Gartner U, Arendt T. Expression of cell cycle-related proteins in developing and adult mouse hippocampus [ J ]. Int J Devl Neuroscience ,2005,23 ( 1 ) : 101 - 112.
  • 2Hata R, Mies G, Wiessner C, et al. A reproducible model of middle cerebral artery occlusion in mice : hemodynamic, biochemical, and magnetic resonance imaging[ J ]. J Cereb Blood Flow Metab, 1998,18 (4) :367 -375.
  • 3Bederson JB,Pitts LH, Tsuji M, et al. Rat middle cerebral artery oc- clusion : evaluation of the model and development of a neurologic ex- amination [ J ]. Stroke, 1986,17 (3) :472 - 476.
  • 4Weinberg RA. The retinoblastoma protein and cell cycle control[ J ]. Ce11,1995,81 (3) :323 -330.
  • 5Malik B, Currais A, Andres A, et al. Loss of neuronal cell cycle con- trol as a mechanism of neurodegeneration in the presenilin-1 Alzhei- merg disease brain[ J]. Cell Cycle ,2008,7 (5) :637 - 646.
  • 6Rashidian J, Iyirhiaro G, Aleyasin H, et al. Multiple cyclin-dependent kinases signals are critical mediators of ischemia/hypoxic neuronal death in vitro and in vivo[ J]. Proc Natl Acad Sci USA,2005,102 (39) : 14080 - 14085.
  • 7Osuga H, Osuga S, Wang F, et al. Cyclin-dependent kinases as a ther- apeutic target for stroke [ J ]. Proc Natl Acad Sci USA, 2000,97 ( 18 ) : 10254 - 10259.
  • 8Nguyen MD, Boudreau M, Kriz J,et al. Cell cycle regulators in the neu- ronal death pathway of amyotrophic lateral sclerosis caused by mutant, superoxide dismutase 1 [ J ]. J Neurosci ,2003,23 (6) :2131 - 2140.
  • 9Park DS, Obeidat A, Giovanni A et al. Cell cycle regulators in neuro- nal death evoked by excitotoxic stress : implications for neurodegenera- tion and its treatment [ J 1. Neurobiol Aging,2000,21 (6) :771 - 781.
  • 10Jordan-Sciutto KL, Malaiyandi LM, Bowser R. Altered distribution of celi cycle transcriptional regulators during Alzheimer disease [ J ]. J Neuropathol Exp Neurol,2002,61 (4) :358 -367.

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