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神经元中 CD200 功能障碍导致突触缺陷和认知障碍。

CD200 dysfunction in neuron contributes to synaptic deficits and cognitive impairment.

机构信息

Department of Neurology, Liaocheng People's Hospital, Liaocheng, Shandong, People's Republic of China, 252000.

Department of Neurology, Liaocheng People's Hospital, Liaocheng, Shandong, People's Republic of China, 252000.

出版信息

Biochem Biophys Res Commun. 2019 Sep 3;516(4):1053-1059. doi: 10.1016/j.bbrc.2019.06.134. Epub 2019 Jul 3.

Abstract

Neuronal CD200 plays critical role in neuron-microglia communication and negatively related to pathological development of Alzheimer's disease, but its contribution retroacts to synaptic function is still not clear. Here, we directly injected adeno-associated virus into hippocampus of APP/PS1 mice to induce neuron-specific CD200 overexpression; subsequently, we detected cognition function, synaptic function, and the microglial responses during AD pathological development. Notably, specific upregulation of neuronal CD200 promoted cognitive function by inhibiting microglial activation and secretion, improving synaptic function, and preventing synaptic loss. To further investigate the role of neuronal CD200 on synaptic function, we depressed CD200 expression in neuron by hippocampal AAV injection and also evaluated microglial activation and cognitive and synaptic function. Interestingly, data revealed that neuronal CD200 deficiency significantly impairs synaptic and cognitive function. Taken these results together, we concluded that neuronal CD200 mediated microglial response and synaptic function during AD pathological development, and provided evidence that neuronal CD200 restoration ameliorates synaptic and cognitive deficits.

摘要

神经元 CD200 在神经元-小胶质细胞通讯中发挥关键作用,与阿尔茨海默病的病理发展呈负相关,但它对突触功能的反作用仍不清楚。在这里,我们直接将腺相关病毒注射到 APP/PS1 小鼠的海马体中,以诱导神经元特异性 CD200 过表达;随后,我们检测了 AD 病理发展过程中的认知功能、突触功能和小胶质细胞反应。值得注意的是,神经元 CD200 的特异性上调通过抑制小胶质细胞激活和分泌、改善突触功能和防止突触丢失来促进认知功能。为了进一步研究神经元 CD200 对突触功能的作用,我们通过海马体 AAV 注射抑制神经元 CD200 的表达,并评估小胶质细胞激活以及认知和突触功能。有趣的是,数据显示神经元 CD200 缺陷显著损害了突触和认知功能。综合这些结果,我们得出结论,神经元 CD200 在 AD 病理发展过程中调节小胶质细胞反应和突触功能,并且提供了神经元 CD200 恢复改善突触和认知缺陷的证据。

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