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胶质细胞源性神经营养因子体外对脊髓运动神经元的作用
引用本文:宋学琴,吴淑玉,李春岩,王丽琴,王晓娟. 胶质细胞源性神经营养因子体外对脊髓运动神经元的作用[J]. 细胞与分子免疫学杂志, 2003, 19(5): 490-492
作者姓名:宋学琴  吴淑玉  李春岩  王丽琴  王晓娟
作者单位:河北医科大学第二医院神经内科,河北,石家庄,050000
摘    要:目的 :观察不同浓度的胶质细胞源性神经营养因子 (GDNF) ,对大鼠胚胎脊髓运动神经元生长活性的作用。方法 :取大鼠胚胎脊髓腹侧组织体外分离 ,进行原代细胞培养 ,应用抗神经微丝单克隆抗体 (mAb)SMI32进行运动神经元的免疫细胞化学染色 ,从细胞形态学及应用MTT比色法 ,研究GDNF对大鼠脊髓运动神经元的影响。结果 :GDNF能明显促进体外培养的大鼠脊髓运动神经元存活及突起的生长 (P <0 .0 5 ) ,且具有剂量依赖的趋势。结论 :不同浓度的GDNF对体外培养的大鼠胚胎脊髓运动神经元 ,有不同程度的促生长作用

关 键 词:胶质细胞源性神经营养因子 脊髓运动神经元 体外培养 抗神经微丝单克隆抗体
文章编号:1007-8738(2003)05-490-03
修稿时间:2002-10-04

Effect of glia cell line-derived neurotrophic factor on cultured spinal motor neurons from embryonic rat
SONG Xue qin,WU Shu yu,LI Chun yan,WANG Li qin,WANG Xiao juan Neurology Department,Second Hospital of Hebei Medical University,Shijiazhuang ,China. Effect of glia cell line-derived neurotrophic factor on cultured spinal motor neurons from embryonic rat[J]. Chinese journal of cellular and molecular immunology, 2003, 19(5): 490-492
Authors:SONG Xue qin  WU Shu yu  LI Chun yan  WANG Li qin  WANG Xiao juan Neurology Department  Second Hospital of Hebei Medical University  Shijiazhuang   China
Affiliation:Department of Neurology,Second Hospital of Hebei Medical University, Shijiazhuang 050000, China.
Abstract:AIM: To observe the effects of various concentrations of glia cell line derived neurotrophic factor (GDNF) on the growth of cultured spinal motor neurons from embryonic rat. METHODS: Neurons were isolated from embryonic rat spinal ventral tissue and then were primarily cultured in vitro . Morphological feature of neurons was examined by immunocytochemical staining with mAb SMI 32. The effect of GDNF on growth of spinal motor neurons was detected by MTT colorimetry. RESULTS: GDNF could significantly enhance the survival and neurite outgrowth of rat spinal motor neurons cultured in vitro in dose dependent tendency. CONCLUSION: Varying concentrations of GDNF can enhance the growth of embryonic rat spinal motor neurons to various extent.
Keywords:glia cell line derived neurotrophic factor  spinal motor neuron  culture  mAb SMI32
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