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二肽基肽酶6缺失影响海马突触发育,并导致认知、学习和记忆方面的行为障碍。

DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory.

作者信息

Lin Lin, Murphy Jonathan G, Karlsson Rose-Marie, Petralia Ronald S, Gutzmann Jakob J, Abebe Daniel, Wang Ya-Xian, Cameron Heather A, Hoffman Dax A

机构信息

Molecular Neurophysiology and Biophysics Section, Program in Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United States.

Section on Neuroplasticity, National Institute of Mental Health, Bethesda, MD, United States.

出版信息

Front Cell Neurosci. 2018 Mar 29;12:84. doi: 10.3389/fncel.2018.00084. eCollection 2018.

Abstract

DPP6 is well known as an auxiliary subunit of Kv4-containing, A-type K channels which regulate dendritic excitability in hippocampal CA1 pyramidal neurons. We have recently reported, however, a novel role for DPP6 in regulating dendritic filopodia formation and stability, affecting synaptic development and function. These results are notable considering recent clinical findings associating DPP6 with neurodevelopmental and intellectual disorders. Here we assessed the behavioral consequences of DPP6 loss. We found that DPP6 knockout (DPP6-KO) mice are impaired in hippocampus-dependent learning and memory. Results from the Morris water maze and T-maze tasks showed that DPP6-KO mice exhibit slower learning and reduced memory performance. DPP6 mouse brain weight is reduced throughout development compared with WT, and imaging results indicated that DPP6 loss affects synaptic structure and motility. Taken together, these results show impaired synaptic development along with spatial learning and memory deficiencies in DPP6-KO mice.

摘要

DPP6作为含Kv4的A型钾通道的辅助亚基而广为人知,该通道调节海马CA1锥体神经元的树突兴奋性。然而,我们最近报道了DPP6在调节树突丝状伪足形成和稳定性、影响突触发育和功能方面的新作用。考虑到最近将DPP6与神经发育和智力障碍相关联的临床发现,这些结果值得关注。在此,我们评估了DPP6缺失的行为后果。我们发现DPP6基因敲除(DPP6-KO)小鼠在海马依赖性学习和记忆方面受损。莫里斯水迷宫和T迷宫任务的结果表明,DPP6-KO小鼠学习较慢且记忆表现降低。与野生型相比,DPP6小鼠脑重量在整个发育过程中均降低,成像结果表明DPP6缺失会影响突触结构和运动性。综上所述,这些结果表明DPP6-KO小鼠存在突触发育受损以及空间学习和记忆缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5580/5884885/1008ae91e7b0/fncel-12-00084-g0001.jpg

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