Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK.
UCL Institute of Cognitive Neuroscience, UCL Queen Square Institute of Neurology, University College London WC1N 3AZ, UK.
Cell Rep. 2020 Jan 28;30(4):1152-1163.e4. doi: 10.1016/j.celrep.2019.12.065.
Altered neural dynamics in the medial prefrontal cortex (mPFC) and hippocampus may contribute to cognitive impairments in the complex chromosomal disorder Down syndrome (DS). Here, we demonstrate non-overlapping behavioral differences associated with distinct abnormalities in hippocampal and mPFC electrophysiology during a canonical spatial working memory task in three partially trisomic mouse models of DS (Dp1Tyb, Dp10Yey, and Dp17Yey) that together cover all regions of homology with human chromosome 21 (Hsa21). Dp1Tyb mice show slower decision-making (unrelated to the gene dose of DYRK1A, which has been implicated in DS cognitive dysfunction) and altered theta dynamics (reduced frequency, increased hippocampal-mPFC coherence, and increased modulation of hippocampal high gamma); Dp10Yey mice show impaired alternation performance and reduced theta modulation of hippocampal low gamma; and Dp17Yey mice are not significantly different from the wild type. These results link specific hippocampal and mPFC circuit dysfunctions to cognitive deficits in DS models and, importantly, map them to discrete regions of Hsa21.
内侧前额叶皮层(mPFC)和海马体中的神经活动改变可能导致复杂染色体疾病唐氏综合征(DS)中的认知障碍。在这里,我们在三个部分三体 DS 小鼠模型(Dp1Tyb、Dp10Yey 和 Dp17Yey)中展示了与海马体和 mPFC 电生理学的独特异常相关的非重叠行为差异,这些模型共同涵盖了与人类染色体 21(Hsa21)同源的所有区域。Dp1Tyb 小鼠表现出较慢的决策速度(与 DYRK1A 的基因剂量无关,该基因与 DS 认知功能障碍有关)和改变的θ波动力学(频率降低、海马体-mPFC 相干性增加以及海马体高频γ的调制增加);Dp10Yey 小鼠表现出交替性能受损和海马体低频γ的θ波调制减少;而 Dp17Yey 小鼠与野生型小鼠没有显著差异。这些结果将特定的海马体和 mPFC 电路功能障碍与 DS 模型中的认知缺陷联系起来,并且重要的是,将它们映射到 Hsa21 的离散区域。