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首页> 外文期刊>Journal of Neuroscience Methods >Low-density neuronal networks cultured using patterned poly-l-lysine on microelectrode arrays.
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Low-density neuronal networks cultured using patterned poly-l-lysine on microelectrode arrays.

机译:在微电极阵列上使用带图案的聚l-赖氨酸培养的低密度神经元网络。

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摘要

Synaptic activity recorded from low-density networks of cultured rat hippocampal neurons was monitored using microelectrode arrays (MEAs). Neuronal networks were patterned with poly-l-lysine (PLL) using microcontact printing (muCP). Polydimethysiloxane (PDMS) stamps were fabricated with relief structures resulting in patterns of 2mum-wide lines for directing process growth and 20mum-diameter circles for cell soma attachment. These circles were aligned to electrode sites. Different densities of neurons were plated in order to assess the minimal neuron density required for development of an active network. Spontaneous activity was observed at 10-14 days in networks using neuron densities as low as 200cells/mm(2). Immunocytochemistry demonstrated the distribution of dendrites along the lines and the location of foci of the presynaptic protein, synaptophysin, on neuron somas and dendrites. Scanning electron microscopy demonstrated that single fluorescent tracks contained multiple processes. Evoked responses of selected portions of the networks were produced by stimulation of specific electrode sites. In addition, the neuronal excitability of the network was increased by the bath application of high K(+) (10-12mM). Application of DNQX, an AMPA antagonist, blocked all spontaneous activity, suggesting that the activity is excitatory and mediated through glutamate receptors.
机译:使用微电极阵列(MEA)监测从培养的大鼠海马神经元的低密度网络记录的突触活动。使用微接触印刷(muCP),用聚-1-赖氨酸(PLL)对神经元网络进行图案化。聚二甲基硅氧烷(PDMS)压模以浮雕结构制成,形成了2mum宽的线用于引导工艺生长,并形成20mm直径的圆用于细胞体附着。这些圆圈与电极部位对齐。电镀不同密度的神经元,以评估开发活动网络所需的最小神经元密度。在使用神经元密度低至200cells / mm(2)的网络中,观察到了10-14天的自发活动。免疫细胞化学表明,树突沿线分布以及突触前蛋白突触素的病灶位置在神经元体和树突上。扫描电子显微镜显示单个荧光轨迹包含多个过程。网络的选定部分的诱发反应是通过刺激特定电极部位产生的。此外,网络的神经元兴奋性通过高K(+)(10-12mM)的沐浴应用而增加。 AMPQ拮抗剂DNQX的使用阻止了所有自发活性,表明该活性是兴奋性的,并通过谷氨酸受体介导。

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