首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Vomeronasal neurons promote synaptic formation on dendritic spines but not dendritic shafts in primary culture of accessory olfactory bulb neurons.
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Vomeronasal neurons promote synaptic formation on dendritic spines but not dendritic shafts in primary culture of accessory olfactory bulb neurons.

机译:在副嗅球神经元的原代培养中,犁鼻神经元促进树突棘上的突触形成,但不促进树突干。

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摘要

To investigate the morphological changes of accessory olfactory bulb (AOB) neurons arising from pheromonal signals, a coculture system of AOB neurons and vomeronasal (VN) neurons had been established. Our previous study indicates that under coculture condition, the density of dendritic spines of an AOB neuron is less and the individual spine-head volume is larger than those under monoculture condition. In this study, to determine whether these differences in the dendrites of AOB neurons reflect the differences in synapse formation and synaptic properties, we observed these cultured cells by electron microscopy. Various synapses were observed under each culture condition. Synapses were classified on the basis of their postsynaptic structure and the size of postsynaptic density (PSD) was measured. Under the coculture condition with VN neurons, synapses on dendritic spines, which formed between AOB neurons, were observed frequently. In contrast, many synapses were formed on dendritic shafts under monoculture condition. The PSD of asymmetrical synapses on the spines under coculture condition was larger than that under monoculture condition. Moreover, some dendrodendritic reciprocal synapses were found only in coculture. We confirmed synapse formation between VN axons and AOB dendrites by immunohistochemical electron microscopy; thus, the characteristics of synapses between AOB neurons are considered to be modified by the synaptic contacts with VN axons.
机译:为了研究由信息素信号引起的副嗅球(AOB)神经元的形态变化,已建立了AOB神经元和犁鼻(VN)神经元的共培养系统。我们以前的研究表明,在共培养条件下,AOB神经元的树突棘密度较小,单个脊柱头体积比在单培养条件下大。在这项研究中,为了确定AOB神经元树突中的这些差异是否反映了突触形成和突触特性的差异,我们通过电子显微镜观察了这些培养的​​细胞。在每种培养条件下观察到各种突触。根据突触后结构对突触进行分类,并测量突触后密度(PSD)的大小。在与VN神经元共培养的条件下,经常观察到AOB神经元之间形成的树突棘突触。相反,在单培养条件下,许多突触形成在树突轴上。共培养条件下棘突不对称突触的PSD大于单培养条件下突棘的PSD。而且,仅在共培养中发现了一些树突状相互的突触。我们通过免疫组织化学电子显微镜证实了VN轴突和AOB树突之间的突触形成。因此,认为AOB神经元之间的突触特征被与VN轴突的突触接触所修饰。

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