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作 者:吴蕾[1] 胡祥友[1] 许浩[2] 王月菊[1] 秦松[2] 李嘉嘉[1] 周江宁[1]
机构地区:[1]安徽医科大学第一附属医院老年病研究所,合肥230022 [2]中国科学技术大学生命科学院,合肥230027
出 处:《安徽医科大学学报》2003年第5期329-333,共5页Acta Universitatis Medicinalis Anhui
基 金:国家 973项目资助课题 (编号 :G19990 5 40 0 7)
摘 要:目的 探讨雌激素对神经干细胞分裂分化的作用。方法 大鼠神经干细胞培养模型加入剂量为 10mg/L 17β 雌二醇和 10mmol/LBrdU ,分别在培养 4、12h取出细胞 ,进行免疫细胞化学标记。结果 培养 4h ,雌二醇组单位面积细胞总数和BrdU标记细胞与对照组比较差别无显著性 (P=0 2 5 9,P =0 0 6 7) ,培养 12h ,雌二醇组细胞BrdU胞核着色变浅 ,胞浆有着色 ,有 4 0 %的细胞可见明显突起 ,单位面积的细胞总数较对照组无显著性改变 (P =0 0 6 ) ,BrdU标记细胞数目减少 (P =0 0 0 3) ,提示分裂细胞减少。另一方面 ,培养 12h时的雌二醇处理组BrdU免疫荧光阳性细胞的光密度 (OD)显著高于对照组 (P <0 0 1)。结论 17β 雌二醇可以抑制大鼠神经干细胞分裂 ,促进神经干细胞分化。Objective To detect the action of 17beta-est r adiol on division and differentiation of neural stem cells. Methods The neural stem cells derived from 12~12.5 d embryonic rat cortex were exposed to 17beta-estradiol (10 mg/L) and coincubated with BrdU to mark new DNA synthesis. Results No differences in the number of total cells and BrdU- immunopositive cells per unit was found between the estradiol and control group after 4h culture(P=0 259, P=0 067). However,after 12 h culture,Brd U-immunopositive cell number was decreased in the estradiol group,compared wit h the control (P=0 003). But the optical density of BrdU-immunopositive ce lls was increased in estradiol group (P<0 01). Also,40% of BrdU-immunopos itive cells with processes were found in estradiol group while only nucleus coul d be seen in the control. There was no difference in total cell number between t he two groups (P=0 06). Conclusion All these results sugge st that estradiol may inhibit division of neural stem cell and induce cell differentiation of morphology.oincubatedwithBrdUtomarknew
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