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作 者:柴继侠[1,2] 于剑锋[1] 陈明军[1] 陈祖林 李瑞锡[1] 彭裕文[1]
机构地区:[1]复旦大学上海医学院人体解剖学与组织胚胎学系,上海200032 [2]蚌埠医学院组织学与胚胎学教研室,蚌埠233030 [3]洛克菲勒大学神经生物学和遗传学实验室,纽约10021
出 处:《解剖学杂志》2010年第4期502-505,F0002,共5页Chinese Journal of Anatomy
基 金:受安徽省高校优秀青年人才基金(2010SQRL125)部分资助
摘 要:目的: 探讨阿尔茨海默病(AD)脑内β-淀粉样蛋白(Aβ)积聚与树突棘蛋白drebrin表达变化之间的关系.方法: 采用免疫细胞化学、ELISA和免疫印迹法等方法检测大脑皮层原代培养的APP/PS1转基因小鼠的神经元和同种野生型(WT)小鼠的神经元Aβ和drebrin的表达.结果: 培养至12d (days in vitro)时,可见Aβ在APP/PS1神经元胞体内聚集,培养基内的Aβ水平也同时升高;此期神经元内drebrin斑点状免疫反应产物分布较为稀疏,drebrin的表达水平下降.18d时,Aβ在胞体内聚集的基础上,向突起内延伸,培养基内的Aβ水平进一步升高;drebrin的表达则明显下降.结论: 原代培养的APP/PS1小鼠神经元内Aβ积聚的同时,树突棘蛋白drebrin的表达下降.提示AD脑内Aβ积聚可能是影响树突棘蛋白drebrin表达的因素之一.Objective: To investigate the relationship between β-amyloid protein (Aβ) accumulation and the expression change of the dendritic spine protein drebrin in the brain of Alzheimer's disease (AD). Methods: The expressions of Aβ and drebrin in primary cultured neurons from the cerebral cortex of the APP/PS1 transgenic and wild type mice by means of immunocy- tochemistry, ELISA and Western blotting. Results: Compared with control neurons from the wild type mice, the Aβ was observed to be gathered in perikarya of the neurons of the APP/PS1 transgenic mice and the Aβ level was increased in the same time in culture medium at 12 days in vitro ; meanwhile, the irnmunoreactive spot of the drebrin was rarely seen, the ex- pression level of drebrin was decreased. In 18 d in vitro, the pericaryon gathered Aβ was observed to be spread into the processes, and the Aβ level in the culture medium was obviously increased; the expression level of drebrin was significantly decreased. Conclusion: These results indicated that accumulation of the Aβin the primary cultured APP/PS1 neurons followed by a decreased expression of the drebrin, which suggested that Aβ accumulation might be one of the reasons of decrease of the drehrin in the brain of AD.
关 键 词:Β-淀粉样蛋白 DREBRIN 阿尔茨海默病 APP/PS1 转基因 神经元 原代培养
分 类 号:R322.81[医药卫生—人体解剖和组织胚胎学]
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