CREB and neuronal selection for memory trace
Despite considerable progress over the past several decades, our understanding of the mechanisms underlying memory encoding, storage, and expression in a complex neural network are far from complete. In particular, how some neurons rather than others are selectively engaged to encode memory remains...
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doaj-78d894adb9c34211b477d81507a62ef82020-11-24T22:58:21ZengFrontiers Media S.A.Frontiers in Neural Circuits1662-51102013-03-01710.3389/fncir.2013.0004446332CREB and neuronal selection for memory traceJieun eKim0Jeong-Tae eKwon1Hyung-Su eKim2Jin-Hee eHan3Korea Advanced Institute of Science and TechnologyKorea Advanced Institute of Science and TechnologyKorea Advanced Institute of Science and TechnologyKorea Advanced Institute of Science and TechnologyDespite considerable progress over the past several decades, our understanding of the mechanisms underlying memory encoding, storage, and expression in a complex neural network are far from complete. In particular, how some neurons rather than others are selectively engaged to encode memory remains largely unknown. Using virus-mediated gene delivery into a small subset of neurons in a given network, molecular imaging of neuronal activity, pharmacological perturbation of specific neurons’ activity and animal behavior assays, recent studies have begun to provide insight into molecular and cellular mechanisms responsible for the selection of neurons for inclusion into a memory trace. Here, we focus on a review of recent findings supporting the hypothesis that the level of the transcription factor CREB (cAMP/Ca2+-response element binding protein) is a key factor governing which neurons are recruited to a given memory trace. These recent findings open a new perspective on memory trace at the neural circuit level and also raise many important questions. Future studies employing more advanced neurobiological techniques for targeting defined populations of neurons and manipulating their activity in time and space in a complex neural network will give answers to these newly emerging questions and extend our understanding of the neurobiological basis of the memory trace.http://journal.frontiersin.org/Journal/10.3389/fncir.2013.00044/fullexcitabilityNeural NetworkCREBdendritic spinememory traceneuronal selection |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jieun eKim Jeong-Tae eKwon Hyung-Su eKim Jin-Hee eHan |
spellingShingle |
Jieun eKim Jeong-Tae eKwon Hyung-Su eKim Jin-Hee eHan CREB and neuronal selection for memory trace Frontiers in Neural Circuits excitability Neural Network CREB dendritic spine memory trace neuronal selection |
author_facet |
Jieun eKim Jeong-Tae eKwon Hyung-Su eKim Jin-Hee eHan |
author_sort |
Jieun eKim |
title |
CREB and neuronal selection for memory trace |
title_short |
CREB and neuronal selection for memory trace |
title_full |
CREB and neuronal selection for memory trace |
title_fullStr |
CREB and neuronal selection for memory trace |
title_full_unstemmed |
CREB and neuronal selection for memory trace |
title_sort |
creb and neuronal selection for memory trace |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neural Circuits |
issn |
1662-5110 |
publishDate |
2013-03-01 |
description |
Despite considerable progress over the past several decades, our understanding of the mechanisms underlying memory encoding, storage, and expression in a complex neural network are far from complete. In particular, how some neurons rather than others are selectively engaged to encode memory remains largely unknown. Using virus-mediated gene delivery into a small subset of neurons in a given network, molecular imaging of neuronal activity, pharmacological perturbation of specific neurons’ activity and animal behavior assays, recent studies have begun to provide insight into molecular and cellular mechanisms responsible for the selection of neurons for inclusion into a memory trace. Here, we focus on a review of recent findings supporting the hypothesis that the level of the transcription factor CREB (cAMP/Ca2+-response element binding protein) is a key factor governing which neurons are recruited to a given memory trace. These recent findings open a new perspective on memory trace at the neural circuit level and also raise many important questions. Future studies employing more advanced neurobiological techniques for targeting defined populations of neurons and manipulating their activity in time and space in a complex neural network will give answers to these newly emerging questions and extend our understanding of the neurobiological basis of the memory trace. |
topic |
excitability Neural Network CREB dendritic spine memory trace neuronal selection |
url |
http://journal.frontiersin.org/Journal/10.3389/fncir.2013.00044/full |
work_keys_str_mv |
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