首页> 美国卫生研究院文献>The Journal of Neuroscience >Reciprocal Homosynaptic and Heterosynaptic Long-Term Plasticity of Corticogeniculate Projection Neurons in Layer VI of the Mouse Visual Cortex
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Reciprocal Homosynaptic and Heterosynaptic Long-Term Plasticity of Corticogeniculate Projection Neurons in Layer VI of the Mouse Visual Cortex

机译:小鼠视觉皮层第六层中成皮质的投射神经元的相互同态和突触的长期可塑性

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摘要

Most neurons in layer VI of the visual cortex project to the dorsal lateral geniculate nucleus (dLGN). These corticogeniculate projection neurons (CG cells) receive top-down synaptic inputs from upper layers (ULs) and bottom-up inputs from the underlying white matter (WM). Use-dependent plasticity of these synapses in layer VI of the cortex has received less attention than in other layers. In the present study, we used a retrograde tracer injected into dLGN to identify CG cells, and, by analyzing EPSPs evoked by electrical stimulation of the UL or WM site, examined whether these synapses show long-term synaptic plasticity. Theta-burst stimulation induced long-term potentiation (LTP) of activated synapses (hom-LTP) and long-term depression (LTD) of nonactivated synapses (het-LTD) in either pathway. The paired-pulse stimulation protocol and the analysis of coefficient variation of EPSPs suggested postsynaptic induction of these changes except UL-induced het-LTD, which may be presynaptic in origin. Intracellular injection of a Ca2+-chelator suggested an involvement of postsynaptic Ca2+ rise in all types of long-term plasticity. Pharmacological analysis indicated that NMDA receptors and type-5 metabotropic glutamate receptors are involved in WM-induced and UL-induced plasticity, respectively. Analysis with inhibitors and/or in transgenic mice suggested an involvement of cannabinoid type 1 receptors and calcineurin in UL-induced and WM-induced het-LTD, respectively. These results suggest that hom-LTP and het-LTD may play a role in switching the top-down or bottom-up regulation of CG cell function and/or in maintaining stability of synaptic transmission efficacy through different molecular mechanisms.
机译:视觉皮层VI层中的大多数神经元都投射到背外侧膝状核(dLGN)。这些成皮质的投射神经元(CG细胞)从上层(UL)接收自上而下的突触输入,从基础白质(WM)接收自下而上的输入。这些突触在皮层第六层的依赖于使用的可塑性比其他层受到较少的关注。在本研究中,我们使用了注入dLGN中的逆行示踪剂来鉴定CG细胞,并通过分析由UL或WM部位的电刺激诱发的EPSP,检查了这些突触是否显示出长期的突触可塑性。 θ爆发刺激可在任一途径中诱导活化突触(hom-LTP)的长期增强(LTP)和未活化突触(het-LTD)的长期抑制(LTD)。配对脉冲刺激方案和EPSPs的系数变化分析表明,除了UL诱导的het-LTD(可能起源于突触前)外,这些变化还发生在突触后。胞内注射Ca 2 + -螯合剂提示突触后Ca 2 + 升高与所有类型的长期可塑性有关。药理分析表明,NMDA受体和5型代谢型谷氨酸受体分别与WM诱导的可塑性和UL诱导的可塑性有关。用抑制剂和/或转基因小鼠进行的分析表明,大麻素1型受体和钙调神经磷酸酶分别参与UL诱导和WM诱导的het-LTD。这些结果表明,hom-LTP和het-LTD可能在改变CG细胞功能的自上而下或自下而上的调节和/或通过不同分子机制维持突触传递功效的稳定性中起作用。

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