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机构地区:[1]华中科技大学同济医学院附属同济医院神经内科,武汉430030
出 处:《神经损伤与功能重建》2013年第6期421-425,共5页Neural Injury and Functional Reconstruction
基 金:国家自然科学基金青年基金(No.81000537)
摘 要:目的:研究NMDA受体NR2B基因对海马成年新生神经元生存的影响。方法:通过Cre-loxp重组酶系统构建NMDA受体NR2B亚型基因单细胞敲除模型。观察NR2B基因敲除神经元的存活情况及其形态发生。结果:在逆转录病毒注射后7、17、28、56 d,NR2Bfl/fl小鼠中,成年海马新生神经元生存比例在各观察时间点一致,与同组野生型神经元无显著性差异。NR2B基因敲除神经元神经元大体形态分化发育与野生型神经元类似,但在17、28 d时顶端树突上的棘突发生显著减少(P<0.01)。结论:NMDA受体NR2B亚型基因敲除对海马成年新生神经元生存无显著性影响,但可影响突触发生。Objective: To investigate the effects of conditional NR2B knock out on selective survival of the adult-born granule cells generated fi'om subgranule zone (SGZ) in the hippocampus. Methods: Using retroviral genetic labeling approaches to mark the adult born neurons with GFP/Cre, the survival of the adult born neurons was evaluated by the ratio of Cre+/Cre granule cells at different time points after viral injection in both the WT and NR2Ba transgenic mice. The development of the newborn neurons was also observed. Results: The ratio of the Cre+/Cre granule cells in the dentate gyms was constant in the both WT and NR2B^rfl/ti transgenic mice at all the time points. Meanwhile, there was no statistical difference in survival ratio between the different genotypes (WT and NR2B^tl/tl mice) at each time point. The development of the NR2B-depletion neurons is similar to that in the WT neurons, however synaptogenesis was reduced significantly at 17 and 28 dpi (P〈0.01). Conclusion: NR2B-containing NMDA receptors are not required for selective survival of the hippocampal adult born granule cells, but for the synaptogenesis.
关 键 词:成年神经发生 NMDA受体NR2B亚型 选择性生存 突触发生
分 类 号:R741[医药卫生—神经病学与精神病学] R741.02[医药卫生—临床医学]
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