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The Corticostriatal System in Dissociated Cell Culture

机译:分离细胞培养中的皮质口系统

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摘要

The sparse connectivity within the striatum in vivo makes the investigation of individual corticostriatal synapses very difficult. Most studies of the corticostriatal input have been done using electrical stimulation under conditions where it is hard to identify the precise origin of the cortical input. We have employed an in vitro dissociated cell culture system that allows the identification of individual corticostriatal pairs and have been developing methods to study individual neuron inputs to striatal neurons. In mixed corticostriatal cultures, neurons had resting activity similar to the system in vivo. Up/down states were obvious and seemed to encompass the entire culture. Mixed cultures of cortical neurons from transgenic mice expressing green fluorescent protein with striatal neurons from wild-type mice of the same developmental stage allowed visual identification of individual candidate corticostriatal pairs. Recordings were performed between 12 and 37 days in vitro (DIV). To investigate synaptic connections we recorded from 69 corticostriatal pairs of which 44 were connected in one direction and 25 reciprocally. Of these connections 41 were corticostriatal (nine inhibitory) and 53 striatocortical (all inhibitory). The observed excitatory responses were of variable amplitude (−10 to −370 pA, n = 32). We found the connections very secure – with negligible failures on repeated stimulation (approximately 1 Hz) of the cortical neuron. Inhibitory corticostriatal responses were also observed (−13 to −314 pA, n = 9). Possibly due to the mixed type of culture we found an inhibitory striatocortical response (−14 to −598 pA, n = 53). We are now recording from neurons in separate compartments to more closely emulate neuroanatomical conditions but still with the possibility of the easier identification of the connectivity.
机译:体内纹状体内的稀疏连通性使得对单个皮质口突触的研究非常困难。在难以确定皮层输入的确切来源的条件下,大多数使用皮质刺激进行皮质上皮输入的研究。我们采用了一种体外分离的细胞培养系统,该系统可识别单个皮质口对,并已在开发研究纹状体神经元的单个神经元输入的方法。在混合皮质上皮培养物中,神经元具有与体内系统相似的静息活动。上下状态很明显,似乎涵盖了整个文化。来自表达绿色荧光蛋白的转基因小鼠的皮层神经元与来自相同发育阶段的野生型小鼠的纹状体神经元的混合培养物,可以目视鉴定单个候选的成骨皮质对。在体外(DIV)的12到37天之间进行记录。为了研究突触连接,我们记录了69对皮层皮质口对,其中44对沿一个方向连接,而25对相互连接。在这些连接中,有41个为皮质骨皮质(抑制性),有53个为皮层皮层(均具有抑制性)。观察到的兴奋反应的幅度是可变的(-10至-370ApA,n = 32)。我们发现连接非常安全-皮层神经元的重复刺激(大约1 Hz)可忽略不计。还观察到抑制性皮层皮质反应(-13至-314 pA,n = 9)。可能由于文化的混合类型,我们发现了抑制纹状体皮层反应(-14至-598 pA,n = 53)。现在,我们正在从单独的隔室中的神经元进行记录,以更紧密地模拟神经解剖学状况,但仍有可能更容易识别连接性。

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