恐怖記憶形成に関与するシナプスの検出法の開発

In the auditory cued fear conditioning, memories are stored in synapses between engram neurons, which increased activity during the memory formation. Although molecular imaging of memory-related synapses contributes to deciphering the molecular basis of memory, there is no established method for vis...

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Published in日本薬理学会年会要旨集 p. 2-B-P-151
Main Authors 大久保, 洋平, 並木, 繁行, 廣瀬, 謙造, 大西, 泰地, 坂本, 寛和
Format Journal Article
LanguageJapanese
Published 公益社団法人 日本薬理学会 2022
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ISSN2435-4953
DOI10.1254/jpssuppl.96.0_2-B-P-151

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Abstract In the auditory cued fear conditioning, memories are stored in synapses between engram neurons, which increased activity during the memory formation. Although molecular imaging of memory-related synapses contributes to deciphering the molecular basis of memory, there is no established method for visualizing them. In this study, we developed a method to selectively visualize synapses between engram neurons, using the c-fos promoter-driven Tet-On system. Tag-fused synaptophysin (tagSyp) and FingR.PSD95 were expressed in presynaptic auditory cortex neurons and postsynaptic lateral amygdala neurons, respectively, in an activity-dependent manner. We found that the number of synapses positive for both tagSyp and FingR.PSD95 in the lateral amygdala was 15-fold higher in mice with cued fear conditioning than in control mice. Thus, we concluded that synapses both positive for tagSyp and FingR.PSD95 correspond to memory-related synapses. Furthermore, combining this method with immunohistochemistry, we found greater amounts of several kinds of synaptic molecules accumulate in memory-related synapses compared to other synapses. It is expected that our method enables comprehensive analysis of molecular changes in synapses induced by fear memory formation.
AbstractList In the auditory cued fear conditioning, memories are stored in synapses between engram neurons, which increased activity during the memory formation. Although molecular imaging of memory-related synapses contributes to deciphering the molecular basis of memory, there is no established method for visualizing them. In this study, we developed a method to selectively visualize synapses between engram neurons, using the c-fos promoter-driven Tet-On system. Tag-fused synaptophysin (tagSyp) and FingR.PSD95 were expressed in presynaptic auditory cortex neurons and postsynaptic lateral amygdala neurons, respectively, in an activity-dependent manner. We found that the number of synapses positive for both tagSyp and FingR.PSD95 in the lateral amygdala was 15-fold higher in mice with cued fear conditioning than in control mice. Thus, we concluded that synapses both positive for tagSyp and FingR.PSD95 correspond to memory-related synapses. Furthermore, combining this method with immunohistochemistry, we found greater amounts of several kinds of synaptic molecules accumulate in memory-related synapses compared to other synapses. It is expected that our method enables comprehensive analysis of molecular changes in synapses induced by fear memory formation.
Author 坂本, 寛和
大西, 泰地
大久保, 洋平
並木, 繁行
廣瀬, 謙造
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  fullname: 大西, 泰地
  organization: 東京大・院医・細胞分子薬理学
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  fullname: 坂本, 寛和
  organization: 東京大・院医・細胞分子薬理学
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Snippet In the auditory cued fear conditioning, memories are stored in synapses between engram neurons, which increased activity during the memory formation. Although...
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SubjectTerms memory
synapse
Title 恐怖記憶形成に関与するシナプスの検出法の開発
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