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 develop...

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Main Authors: Lin Lin, Jonathan G. Murphy, Rose-Marie Karlsson, Ronald S. Petralia, Jakob J. Gutzmann, Daniel Abebe, Ya-Xian Wang, Heather A. Cameron, Dax A. Hoffman
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fncel.2018.00084/full
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spelling doaj-05a6499f4fe14158879ccafb343662c32020-11-24T22:45:35ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022018-03-011210.3389/fncel.2018.00084343856DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and MemoryLin Lin0Jonathan G. Murphy1Rose-Marie Karlsson2Ronald S. Petralia3Jakob J. Gutzmann4Daniel Abebe5Ya-Xian Wang6Heather A. Cameron7Dax A. Hoffman8Molecular Neurophysiology and Biophysics Section, Program in Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United StatesMolecular Neurophysiology and Biophysics Section, Program in Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United StatesSection on Neuroplasticity, National Institute of Mental Health, Bethesda, MD, United StatesAdvanced Imaging Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, United StatesMolecular Neurophysiology and Biophysics Section, Program in Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United StatesMolecular Neurophysiology and Biophysics Section, Program in Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United StatesAdvanced Imaging Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, United StatesSection on Neuroplasticity, National Institute of Mental Health, Bethesda, MD, United StatesMolecular Neurophysiology and Biophysics Section, Program in Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, United StatesDPP6 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.http://journal.frontiersin.org/article/10.3389/fncel.2018.00084/fullDPP6neurodevelopmentlearning and memoryautism spectrum disorder
collection DOAJ
language English
format Article
sources DOAJ
author Lin Lin
Jonathan G. Murphy
Rose-Marie Karlsson
Ronald S. Petralia
Jakob J. Gutzmann
Daniel Abebe
Ya-Xian Wang
Heather A. Cameron
Dax A. Hoffman
spellingShingle Lin Lin
Jonathan G. Murphy
Rose-Marie Karlsson
Ronald S. Petralia
Jakob J. Gutzmann
Daniel Abebe
Ya-Xian Wang
Heather A. Cameron
Dax A. Hoffman
DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory
Frontiers in Cellular Neuroscience
DPP6
neurodevelopment
learning and memory
autism spectrum disorder
author_facet Lin Lin
Jonathan G. Murphy
Rose-Marie Karlsson
Ronald S. Petralia
Jakob J. Gutzmann
Daniel Abebe
Ya-Xian Wang
Heather A. Cameron
Dax A. Hoffman
author_sort Lin Lin
title DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory
title_short DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory
title_full DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory
title_fullStr DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory
title_full_unstemmed DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory
title_sort dpp6 loss impacts hippocampal synaptic development and induces behavioral impairments in recognition, learning and memory
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2018-03-01
description 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.
topic DPP6
neurodevelopment
learning and memory
autism spectrum disorder
url http://journal.frontiersin.org/article/10.3389/fncel.2018.00084/full
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