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Hippocampal Network Oscillations in APP/APLP2-Deficient Mice

The physiological function of amyloid precursor protein (APP) and its two homologues APP-like protein 1 (APLP1) and 2 (APLP2) is largely unknown. Previous work suggests that lack of APP or APLP2 impairs synaptic plasticity and spatial learning. There is, however, almost no data on the role of APP or...

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Autores principales: Zhang, Xiaomin, Herrmann, Ulrike, Weyer, Sascha W., Both, Martin, Müller, Ulrike C., Korte, Martin, Draguhn, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621758/
https://www.ncbi.nlm.nih.gov/pubmed/23585881
http://dx.doi.org/10.1371/journal.pone.0061198
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author Zhang, Xiaomin
Herrmann, Ulrike
Weyer, Sascha W.
Both, Martin
Müller, Ulrike C.
Korte, Martin
Draguhn, Andreas
author_facet Zhang, Xiaomin
Herrmann, Ulrike
Weyer, Sascha W.
Both, Martin
Müller, Ulrike C.
Korte, Martin
Draguhn, Andreas
author_sort Zhang, Xiaomin
collection PubMed
description The physiological function of amyloid precursor protein (APP) and its two homologues APP-like protein 1 (APLP1) and 2 (APLP2) is largely unknown. Previous work suggests that lack of APP or APLP2 impairs synaptic plasticity and spatial learning. There is, however, almost no data on the role of APP or APLP at the network level which forms a critical interface between cellular functions and behavior. We have therefore investigated memory-related synaptic and network functions in hippocampal slices from three lines of transgenic mice: APPsα-KI (mice expressing extracellular fragment of APP, corresponding to the secreted APPsα ectodomain), APLP2-KO, and combined APPsα-KI/APLP2-KO (APPsα-DM for “double mutants”). We analyzed two prominent patterns of network activity, gamma oscillations and sharp-wave ripple complexes (SPW-R). Both patterns were generally preserved in all strains. We find, however, a significantly reduced frequency of gamma oscillations in CA3 of APLP2-KO mice in comparison to APPsα-KI and WT mice. Network activity, basic synaptic transmission and short-term plasticity were unaltered in the combined mutants (APPsα-DM) which showed, however, reduced long-term potentiation (LTP). Together, our data indicate that APLP2 and the intracellular domain of APP are not essential for coherent activity patterns in the hippocampus, but have subtle effects on synaptic plasticity and fine-tuning of network oscillations.
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spelling pubmed-36217582013-04-12 Hippocampal Network Oscillations in APP/APLP2-Deficient Mice Zhang, Xiaomin Herrmann, Ulrike Weyer, Sascha W. Both, Martin Müller, Ulrike C. Korte, Martin Draguhn, Andreas PLoS One Research Article The physiological function of amyloid precursor protein (APP) and its two homologues APP-like protein 1 (APLP1) and 2 (APLP2) is largely unknown. Previous work suggests that lack of APP or APLP2 impairs synaptic plasticity and spatial learning. There is, however, almost no data on the role of APP or APLP at the network level which forms a critical interface between cellular functions and behavior. We have therefore investigated memory-related synaptic and network functions in hippocampal slices from three lines of transgenic mice: APPsα-KI (mice expressing extracellular fragment of APP, corresponding to the secreted APPsα ectodomain), APLP2-KO, and combined APPsα-KI/APLP2-KO (APPsα-DM for “double mutants”). We analyzed two prominent patterns of network activity, gamma oscillations and sharp-wave ripple complexes (SPW-R). Both patterns were generally preserved in all strains. We find, however, a significantly reduced frequency of gamma oscillations in CA3 of APLP2-KO mice in comparison to APPsα-KI and WT mice. Network activity, basic synaptic transmission and short-term plasticity were unaltered in the combined mutants (APPsα-DM) which showed, however, reduced long-term potentiation (LTP). Together, our data indicate that APLP2 and the intracellular domain of APP are not essential for coherent activity patterns in the hippocampus, but have subtle effects on synaptic plasticity and fine-tuning of network oscillations. Public Library of Science 2013-04-09 /pmc/articles/PMC3621758/ /pubmed/23585881 http://dx.doi.org/10.1371/journal.pone.0061198 Text en © 2013 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Xiaomin
Herrmann, Ulrike
Weyer, Sascha W.
Both, Martin
Müller, Ulrike C.
Korte, Martin
Draguhn, Andreas
Hippocampal Network Oscillations in APP/APLP2-Deficient Mice
title Hippocampal Network Oscillations in APP/APLP2-Deficient Mice
title_full Hippocampal Network Oscillations in APP/APLP2-Deficient Mice
title_fullStr Hippocampal Network Oscillations in APP/APLP2-Deficient Mice
title_full_unstemmed Hippocampal Network Oscillations in APP/APLP2-Deficient Mice
title_short Hippocampal Network Oscillations in APP/APLP2-Deficient Mice
title_sort hippocampal network oscillations in app/aplp2-deficient mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3621758/
https://www.ncbi.nlm.nih.gov/pubmed/23585881
http://dx.doi.org/10.1371/journal.pone.0061198
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