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

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 devel...

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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884885/
https://www.ncbi.nlm.nih.gov/pubmed/29651237
http://dx.doi.org/10.3389/fncel.2018.00084
Descripción
Sumario: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 in vitro 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.