Nishimura Masataka, Owens James, Swann John W
The Cain Foundation Laboratories, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
Neurobiol Dis. 2008 Feb;29(2):267-77. doi: 10.1016/j.nbd.2007.08.018. Epub 2007 Sep 12.
Experiments reported here were motivated by studies in both human epilepsy and animal models in which stunted dendritic arbors are observed. Our goal was to determine if chronic network hyperexcitability alters dendritic growth. Experiments were conducted in hippocampal slice cultures obtained from infant mice that express the fluorescent protein YFP in CA1 hippocampal pyramidal cells. Results showed that 4 days of GABAa receptor blockade produced a 40% decrease in basilar dendritic length. When dendritic growth was followed over this 4-day interval, dendrites in untreated slices doubled in length, however dendrites in bicuculline treated cultures failed to grow. These effects were suppressed by APV - suggesting a dependence on NMDA receptor activation. Activation of the transcription factor CREB was also decreased by chronic network hyperexcitability - pointing to possible molecular events underlying the observed suppression of growth. Taken together, our results suggest that chronic hippocampal network hyperexcitability limits dendritic growth.
此处报道的实验受到了人类癫痫和动物模型研究的启发,在这些研究中观察到了发育不良的树突分支。我们的目标是确定慢性网络过度兴奋是否会改变树突生长。实验在从幼鼠获得的海马切片培养物中进行,这些幼鼠的CA1海马锥体细胞中表达荧光蛋白YFP。结果显示,4天的GABAa受体阻断使基底树突长度减少了40%。当在这4天的间隔内跟踪树突生长时,未处理切片中的树突长度增加了一倍,然而荷包牡丹碱处理培养物中的树突未能生长。这些效应被APV抑制——表明依赖于NMDA受体激活。慢性网络过度兴奋也会降低转录因子CREB的激活——指出了观察到的生长抑制背后可能的分子事件。综上所述,我们的结果表明慢性海马网络过度兴奋会限制树突生长。