Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.

Neurabin is a scaffolding protein that interacts with actin and protein phosphatase-1. Highly enriched in the dendritic spine, neurabin is important for spine morphogenesis and synaptic formation. However, less is known about the role of neurabin in hippocampal plasticity and its possible effect on...

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Main Authors: Long-Jun Wu, Ming Ren, Hansen Wang, Susan S Kim, Xiaoyan Cao, Min Zhuo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18183288/pdf/?tool=EBI
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spelling doaj-97cf09fbba8644b58e512bf00bc034802021-03-03T22:26:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-0131e140710.1371/journal.pone.0001407Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.Long-Jun WuMing RenHansen WangSusan S KimXiaoyan CaoMin ZhuoNeurabin is a scaffolding protein that interacts with actin and protein phosphatase-1. Highly enriched in the dendritic spine, neurabin is important for spine morphogenesis and synaptic formation. However, less is known about the role of neurabin in hippocampal plasticity and its possible effect on behavioral functions. Using neurabin knockout (KO) mice, here we studied the function of neurabin in hippocampal synaptic transmission, plasticity and behavioral memory. We demonstrated that neurabin KO mice showed a deficit in contextual fear memory but not auditory fear memory. Whole-cell patch clamp recordings in the hippocampal CA1 neurons showed that long-term potentiation (LTP) was significantly reduced, whereas long-term depression (LTD) was unaltered in neurabin KO mice. Moreover, increased AMPA receptor but not NMDA receptor-mediated synaptic transmission was found in neurabin KO mice, and is accompanied by decreased phosphorylation of GluR1 at the PKA site (Ser845) but no change at the CaMKII/PKC site (Ser831). Pre-conditioning with LTD induction rescued the following LTP in neurabin KO mice, suggesting the loss of LTP may be due to the saturated synaptic transmission. Our results indicate that neurabin regulates contextual fear memory and LTP in hippocampal CA1 pyramidal neurons.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18183288/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Long-Jun Wu
Ming Ren
Hansen Wang
Susan S Kim
Xiaoyan Cao
Min Zhuo
spellingShingle Long-Jun Wu
Ming Ren
Hansen Wang
Susan S Kim
Xiaoyan Cao
Min Zhuo
Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.
PLoS ONE
author_facet Long-Jun Wu
Ming Ren
Hansen Wang
Susan S Kim
Xiaoyan Cao
Min Zhuo
author_sort Long-Jun Wu
title Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.
title_short Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.
title_full Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.
title_fullStr Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.
title_full_unstemmed Neurabin contributes to hippocampal long-term potentiation and contextual fear memory.
title_sort neurabin contributes to hippocampal long-term potentiation and contextual fear memory.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-01-01
description Neurabin is a scaffolding protein that interacts with actin and protein phosphatase-1. Highly enriched in the dendritic spine, neurabin is important for spine morphogenesis and synaptic formation. However, less is known about the role of neurabin in hippocampal plasticity and its possible effect on behavioral functions. Using neurabin knockout (KO) mice, here we studied the function of neurabin in hippocampal synaptic transmission, plasticity and behavioral memory. We demonstrated that neurabin KO mice showed a deficit in contextual fear memory but not auditory fear memory. Whole-cell patch clamp recordings in the hippocampal CA1 neurons showed that long-term potentiation (LTP) was significantly reduced, whereas long-term depression (LTD) was unaltered in neurabin KO mice. Moreover, increased AMPA receptor but not NMDA receptor-mediated synaptic transmission was found in neurabin KO mice, and is accompanied by decreased phosphorylation of GluR1 at the PKA site (Ser845) but no change at the CaMKII/PKC site (Ser831). Pre-conditioning with LTD induction rescued the following LTP in neurabin KO mice, suggesting the loss of LTP may be due to the saturated synaptic transmission. Our results indicate that neurabin regulates contextual fear memory and LTP in hippocampal CA1 pyramidal neurons.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18183288/pdf/?tool=EBI
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AT susanskim neurabincontributestohippocampallongtermpotentiationandcontextualfearmemory
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