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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2008-01-01
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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 |
work_keys_str_mv |
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