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作 者:刘宝华[1] 沙莹[2] 白光辉[3] 李勇[4] 邬伟[4] 商萍[1] 王小同[1]
机构地区:[1]温州医科大学附属第二医院康复中心,浙江温州325027 [2]吉林大学第一医院干部病房,吉林长春130021 [3]温州医科大学附属第二医院影像科,浙江温州325027 [4]温州医科大学附属第二医院神经内科,浙江温州325027
出 处:《温州医学院学报》2014年第5期329-333,337,共6页Journal of Wenzhou Medical College
基 金:浙江省医药卫生平台骨干人才计划项目(2013RCA036)
摘 要:目的:研究造血干细胞动员剂重组人粒细胞集落刺激因子(rhG-CSF)对脑缺血神经系统具有保护作用的蛋白质组学机制。方法:本实验利用脑缺血再灌注大鼠模型(tMCAO模型)在再灌注2 h后颈部皮下注射rhG-CSF,在灌注后14 d提取大脑皮质蛋白进行双向电泳。结果:缺血再灌注损伤(模型组)大鼠与假手术组大鼠比较,筛选到56个差异表达蛋白质点,其中17个上调,39个下调,应用基质辅助激光解吸电离飞行时间质谱仪(MALDI-TOF-MS)得到肽质量指纹图,输入美国国立生物技术信息中心(NCBI)蛋白质数据库进行检索,并在Swiss-Prot数据库中进一步验证,鉴定出其中19个为已知蛋白质。而经过人粒细胞集落刺激因子(G-CSF)治疗(G-CSF治疗组)大鼠与模型组大鼠比较,筛选出35个蛋白质点,其中16个下调,19个上调,其中鉴定为已知蛋白质的有6个,分别为二氢嘧啶酶相关蛋白2、胶质纤维酸性蛋白、内皮黏蛋白、Rho GDP解离抑制因子、Rab GDP解离抑制因子、鸟嘌呤核苷酸结合蛋白。结论:脑缺血后大鼠脑组织蛋白质表达发生变化,G-CSF在脑缺血亚急性期可能通过调节多种神经再生相关蛋白质的表达,参与保护脑缺血的神经元。Objective: To research the relation between difference protein with neuron protective effect of G-CSF in ischemia-reperfusion rats brain by using proteomics.Methods: Twenty-four experimental Wistar rats were divide into 3 groups, control group, rats cured by G-CSF group (G-CSF group), ischemia-reperfusion injured rats group (I/R group). Ischemia-reperfusion injury rats model was generated by using Koizumi’s way in G group and I/R group, one nylon thread was used to block the rats middle cerebral artery and reperfused after 2 hours. G-CSF (50μg/kg/d) was injected subcutaneously on rats’ backs for successive 5 days in G-CSF group. Rats were executed and decapitated after 14 days after reperfusion to get the brain respectively. Sodium chloride injection was used in I/R group and control group.Cortex proteins were extracted in the 3 groups of rats. Then the maps of the proteins were established by DIGE (differential gel electrophoresis, DIGE). The altered protein spots were identiifed with MALDI-TOF-MS and database searching.Results: Compared with the contrl group, the I/R group gained 56 differential protein spots, 39 spots expressed lowly, and 17 spots high. Compared with I/R group, the G-SCF group gained 35 differential protein spots, 16 spots expressed lowly, and 19 spots high, identiifed 6 protein spots, including dihydropyrimidinase-associated protein 2, glial ifbrillary acidic protein, endo-mucin, Rho GDP dissociation inhibitor, Rab GDP dissociation inhibitor and guanine-nucleotide-binding protein. Conclusion: G-CSF is involved in neuroprotection after brain ischemia, possibly by regulating the expression of various neural regeneration-associated proteins at the subacute stage.
关 键 词:粒细胞集落刺激因子 脑缺血 蛋白质组 神经再生 大鼠
分 类 号:R743[医药卫生—神经病学与精神病学]
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