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体外培养的啮齿类海马神经元髓鞘形成。

Myelination of rodent hippocampal neurons in culture.

机构信息

Neuroscience Graduate Studies Program, The Ohio State University, Columbus, Ohio, USA.

出版信息

Nat Protoc. 2012 Oct;7(10):1774-82. doi: 10.1038/nprot.2012.100. Epub 2012 Sep 6.

Abstract

Axons of various hippocampal neurons are myelinated mainly postnatally, which is important for the proper function of neural circuits. Demyelination in the hippocampus has been observed in patients with multiple sclerosis, Alzheimer's disease or temporal lobe epilepsy. However, very little is known about the mechanisms and exact functions of the interaction between the myelin-making oligodendrocytes and the axons within the hippocampus. This is mainly attributable to the lack of a system suitable for molecular studies. We recently established a new myelin coculture from embryonic day (E) 18 rat embryos consisting of hippocampal neurons and oligodendrocytes, with which we identified a novel intra-axonal signaling pathway regulating the juxtaparanodal clustering of Kv1.2 channels. Here we describe the detailed protocol for this new coculture. It takes about 5 weeks to set up and use the system. This coculture is particularly useful for studying myelin-mediated regulation of ion channel trafficking and for understanding how neuronal excitability and synaptic transmission are regulated by myelination.

摘要

各种海马神经元的轴突主要在出生后髓鞘化,这对于神经回路的正常功能很重要。在多发性硬化症、阿尔茨海默病或颞叶癫痫患者中,已经观察到海马脱髓鞘。然而,对于少突胶质细胞和海马内轴突之间相互作用的机制和确切功能知之甚少。这主要归因于缺乏适合分子研究的系统。我们最近从胚胎期 (E) 18 天大鼠胚胎中建立了一种新的髓鞘共培养物,其中包含海马神经元和少突胶质细胞,我们用其鉴定了一种调节 Kv1.2 通道近旁节簇集的新型轴内信号通路。在这里,我们将详细描述该新共培养系统的建立过程。建立和使用该系统大约需要 5 周的时间。该共培养物特别适用于研究髓鞘介导的离子通道运输调节以及了解髓鞘如何调节神经元兴奋性和突触传递。

相似文献

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Myelination of rodent hippocampal neurons in culture.体外培养的啮齿类海马神经元髓鞘形成。
Nat Protoc. 2012 Oct;7(10):1774-82. doi: 10.1038/nprot.2012.100. Epub 2012 Sep 6.
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Neuron/Oligodendrocyte Myelination Coculture.神经元/少突胶质细胞共培养
Methods Mol Biol. 2018;1791:131-144. doi: 10.1007/978-1-4939-7862-5_10.

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