Loading…

Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia

Microglia have been suggested to be involved in the underlying mechanism of conditional fear memory formation by regulating inflammatory cytokines. However, the mechanism linking microglia and neuronal activity related to fear conditioning remains unclear. This study characterized the transcription...

Full description

Saved in:
Bibliographic Details
Published in:Brain research bulletin 2022-10, Vol.189, p.57-68
Main Authors: Yu, Zhiqian, Sakai, Mai, Fukushima, Hotaka, Ono, Chiaki, Kikuchi, Yoshie, Koyama, Ryuta, Matsui, Ko, Furuyashiki, Tomoyuki, Kida, Satoshi, Tomita, Hiroaki
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c475t-dce22a06a9132cda67eda4acf391c8f15c8ef50e0e074b088e4f56de7132e1c13
cites cdi_FETCH-LOGICAL-c475t-dce22a06a9132cda67eda4acf391c8f15c8ef50e0e074b088e4f56de7132e1c13
container_end_page 68
container_issue
container_start_page 57
container_title Brain research bulletin
container_volume 189
creator Yu, Zhiqian
Sakai, Mai
Fukushima, Hotaka
Ono, Chiaki
Kikuchi, Yoshie
Koyama, Ryuta
Matsui, Ko
Furuyashiki, Tomoyuki
Kida, Satoshi
Tomita, Hiroaki
description Microglia have been suggested to be involved in the underlying mechanism of conditional fear memory formation by regulating inflammatory cytokines. However, the mechanism linking microglia and neuronal activity related to fear conditioning remains unclear. This study characterized the transcription profile of microglia in a fear memory conditional mouse model. Compared with those in control mice microglia, the most significantly induced genes were synapse-related, whereas immune-related genes were reduced due to fear memory consolidation. Whilst the increased expression of synapse-related genes was reversed after fear memory extinction, that of immunological genes was not, strongly suggesting a connection between microglia, neurons, and a dysregulated immune response following contextual fear conditioning. Furthermore, in the hippocampal microglia, we found that the expression of neurotransmitter release regulators, γ-aminobutyric acid (GABA) receptor GABRB3 and synapsin 1/2, increased under fear memory consolidation and restored (decreased) after extinction. In addition, compared with the transcription profile in peripheral monocytes, few overlapping genes were not enriched in biological processes. Taken together, the identified conditional fear stress-induced changes in mouse microglial transcription profiles suggest that microglia-neuron communication mediates contextual fear conditioning. •Synapse-related genes in microglia are changed by contextual fear conditioning.•Consolidation of fear memory induces immune dysfunction in microglia.•Microglial GABRB3 and Synapsin are changed during contextual fear conditioning.•Transcriptional profiles in microglia are different from the peripheral monocytes.
doi_str_mv 10.1016/j.brainresbull.2022.08.017
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2704868859</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0361923022002118</els_id><sourcerecordid>2704868859</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-dce22a06a9132cda67eda4acf391c8f15c8ef50e0e074b088e4f56de7132e1c13</originalsourceid><addsrcrecordid>eNqNkE9LxDAQxYMouK5-h-DJS2uStknqTda_sOBFb0LIptOSpU1rkop-e1PWg0eZwzDwe483D6FLSnJKKL_e5zuvrfMQdnPf54wwlhOZEyqO0IpKUWRMlOIYrUjBaVazgpyisxD2hBAuK75C75vRRfiKs-5xC9pjM7rGRjs66zrsoZt7HSHg8O30FCDzsNwN7sABjl67YLydFh5bh4dxDoAHa_zY9Vafo5NW9wEufvcavT3cv26esu3L4_PmdpuZUlQxawwwpgnXNS2YaTQX0OhSm7aoqZEtrYyEtiKQRpQ7IiWUbcUbEAkHamixRlcH38mPHzOEqAYbDPS9dpASKSZIKbmUVZ3QmwOaIobgoVWTt4P234oStVSq9upvpWqpVBGpUqVJfHcQQ3rm04JXwVhwBhrrwUTVjPY_Nj-upong</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2704868859</pqid></control><display><type>article</type><title>Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia</title><source>ScienceDirect Freedom Collection</source><creator>Yu, Zhiqian ; Sakai, Mai ; Fukushima, Hotaka ; Ono, Chiaki ; Kikuchi, Yoshie ; Koyama, Ryuta ; Matsui, Ko ; Furuyashiki, Tomoyuki ; Kida, Satoshi ; Tomita, Hiroaki</creator><creatorcontrib>Yu, Zhiqian ; Sakai, Mai ; Fukushima, Hotaka ; Ono, Chiaki ; Kikuchi, Yoshie ; Koyama, Ryuta ; Matsui, Ko ; Furuyashiki, Tomoyuki ; Kida, Satoshi ; Tomita, Hiroaki</creatorcontrib><description>Microglia have been suggested to be involved in the underlying mechanism of conditional fear memory formation by regulating inflammatory cytokines. However, the mechanism linking microglia and neuronal activity related to fear conditioning remains unclear. This study characterized the transcription profile of microglia in a fear memory conditional mouse model. Compared with those in control mice microglia, the most significantly induced genes were synapse-related, whereas immune-related genes were reduced due to fear memory consolidation. Whilst the increased expression of synapse-related genes was reversed after fear memory extinction, that of immunological genes was not, strongly suggesting a connection between microglia, neurons, and a dysregulated immune response following contextual fear conditioning. Furthermore, in the hippocampal microglia, we found that the expression of neurotransmitter release regulators, γ-aminobutyric acid (GABA) receptor GABRB3 and synapsin 1/2, increased under fear memory consolidation and restored (decreased) after extinction. In addition, compared with the transcription profile in peripheral monocytes, few overlapping genes were not enriched in biological processes. Taken together, the identified conditional fear stress-induced changes in mouse microglial transcription profiles suggest that microglia-neuron communication mediates contextual fear conditioning. •Synapse-related genes in microglia are changed by contextual fear conditioning.•Consolidation of fear memory induces immune dysfunction in microglia.•Microglial GABRB3 and Synapsin are changed during contextual fear conditioning.•Transcriptional profiles in microglia are different from the peripheral monocytes.</description><identifier>ISSN: 0361-9230</identifier><identifier>EISSN: 1873-2747</identifier><identifier>DOI: 10.1016/j.brainresbull.2022.08.017</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>Fear memory ; Microarray ; Microglia ; Synapsin ; γ-aminobutyric acid (GABA)</subject><ispartof>Brain research bulletin, 2022-10, Vol.189, p.57-68</ispartof><rights>2022 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-dce22a06a9132cda67eda4acf391c8f15c8ef50e0e074b088e4f56de7132e1c13</citedby><cites>FETCH-LOGICAL-c475t-dce22a06a9132cda67eda4acf391c8f15c8ef50e0e074b088e4f56de7132e1c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Yu, Zhiqian</creatorcontrib><creatorcontrib>Sakai, Mai</creatorcontrib><creatorcontrib>Fukushima, Hotaka</creatorcontrib><creatorcontrib>Ono, Chiaki</creatorcontrib><creatorcontrib>Kikuchi, Yoshie</creatorcontrib><creatorcontrib>Koyama, Ryuta</creatorcontrib><creatorcontrib>Matsui, Ko</creatorcontrib><creatorcontrib>Furuyashiki, Tomoyuki</creatorcontrib><creatorcontrib>Kida, Satoshi</creatorcontrib><creatorcontrib>Tomita, Hiroaki</creatorcontrib><title>Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia</title><title>Brain research bulletin</title><description>Microglia have been suggested to be involved in the underlying mechanism of conditional fear memory formation by regulating inflammatory cytokines. However, the mechanism linking microglia and neuronal activity related to fear conditioning remains unclear. This study characterized the transcription profile of microglia in a fear memory conditional mouse model. Compared with those in control mice microglia, the most significantly induced genes were synapse-related, whereas immune-related genes were reduced due to fear memory consolidation. Whilst the increased expression of synapse-related genes was reversed after fear memory extinction, that of immunological genes was not, strongly suggesting a connection between microglia, neurons, and a dysregulated immune response following contextual fear conditioning. Furthermore, in the hippocampal microglia, we found that the expression of neurotransmitter release regulators, γ-aminobutyric acid (GABA) receptor GABRB3 and synapsin 1/2, increased under fear memory consolidation and restored (decreased) after extinction. In addition, compared with the transcription profile in peripheral monocytes, few overlapping genes were not enriched in biological processes. Taken together, the identified conditional fear stress-induced changes in mouse microglial transcription profiles suggest that microglia-neuron communication mediates contextual fear conditioning. •Synapse-related genes in microglia are changed by contextual fear conditioning.•Consolidation of fear memory induces immune dysfunction in microglia.•Microglial GABRB3 and Synapsin are changed during contextual fear conditioning.•Transcriptional profiles in microglia are different from the peripheral monocytes.</description><subject>Fear memory</subject><subject>Microarray</subject><subject>Microglia</subject><subject>Synapsin</subject><subject>γ-aminobutyric acid (GABA)</subject><issn>0361-9230</issn><issn>1873-2747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqNkE9LxDAQxYMouK5-h-DJS2uStknqTda_sOBFb0LIptOSpU1rkop-e1PWg0eZwzDwe483D6FLSnJKKL_e5zuvrfMQdnPf54wwlhOZEyqO0IpKUWRMlOIYrUjBaVazgpyisxD2hBAuK75C75vRRfiKs-5xC9pjM7rGRjs66zrsoZt7HSHg8O30FCDzsNwN7sABjl67YLydFh5bh4dxDoAHa_zY9Vafo5NW9wEufvcavT3cv26esu3L4_PmdpuZUlQxawwwpgnXNS2YaTQX0OhSm7aoqZEtrYyEtiKQRpQ7IiWUbcUbEAkHamixRlcH38mPHzOEqAYbDPS9dpASKSZIKbmUVZ3QmwOaIobgoVWTt4P234oStVSq9upvpWqpVBGpUqVJfHcQQ3rm04JXwVhwBhrrwUTVjPY_Nj-upong</recordid><startdate>20221015</startdate><enddate>20221015</enddate><creator>Yu, Zhiqian</creator><creator>Sakai, Mai</creator><creator>Fukushima, Hotaka</creator><creator>Ono, Chiaki</creator><creator>Kikuchi, Yoshie</creator><creator>Koyama, Ryuta</creator><creator>Matsui, Ko</creator><creator>Furuyashiki, Tomoyuki</creator><creator>Kida, Satoshi</creator><creator>Tomita, Hiroaki</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20221015</creationdate><title>Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia</title><author>Yu, Zhiqian ; Sakai, Mai ; Fukushima, Hotaka ; Ono, Chiaki ; Kikuchi, Yoshie ; Koyama, Ryuta ; Matsui, Ko ; Furuyashiki, Tomoyuki ; Kida, Satoshi ; Tomita, Hiroaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-dce22a06a9132cda67eda4acf391c8f15c8ef50e0e074b088e4f56de7132e1c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Fear memory</topic><topic>Microarray</topic><topic>Microglia</topic><topic>Synapsin</topic><topic>γ-aminobutyric acid (GABA)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Zhiqian</creatorcontrib><creatorcontrib>Sakai, Mai</creatorcontrib><creatorcontrib>Fukushima, Hotaka</creatorcontrib><creatorcontrib>Ono, Chiaki</creatorcontrib><creatorcontrib>Kikuchi, Yoshie</creatorcontrib><creatorcontrib>Koyama, Ryuta</creatorcontrib><creatorcontrib>Matsui, Ko</creatorcontrib><creatorcontrib>Furuyashiki, Tomoyuki</creatorcontrib><creatorcontrib>Kida, Satoshi</creatorcontrib><creatorcontrib>Tomita, Hiroaki</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Zhiqian</au><au>Sakai, Mai</au><au>Fukushima, Hotaka</au><au>Ono, Chiaki</au><au>Kikuchi, Yoshie</au><au>Koyama, Ryuta</au><au>Matsui, Ko</au><au>Furuyashiki, Tomoyuki</au><au>Kida, Satoshi</au><au>Tomita, Hiroaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia</atitle><jtitle>Brain research bulletin</jtitle><date>2022-10-15</date><risdate>2022</risdate><volume>189</volume><spage>57</spage><epage>68</epage><pages>57-68</pages><issn>0361-9230</issn><eissn>1873-2747</eissn><abstract>Microglia have been suggested to be involved in the underlying mechanism of conditional fear memory formation by regulating inflammatory cytokines. However, the mechanism linking microglia and neuronal activity related to fear conditioning remains unclear. This study characterized the transcription profile of microglia in a fear memory conditional mouse model. Compared with those in control mice microglia, the most significantly induced genes were synapse-related, whereas immune-related genes were reduced due to fear memory consolidation. Whilst the increased expression of synapse-related genes was reversed after fear memory extinction, that of immunological genes was not, strongly suggesting a connection between microglia, neurons, and a dysregulated immune response following contextual fear conditioning. Furthermore, in the hippocampal microglia, we found that the expression of neurotransmitter release regulators, γ-aminobutyric acid (GABA) receptor GABRB3 and synapsin 1/2, increased under fear memory consolidation and restored (decreased) after extinction. In addition, compared with the transcription profile in peripheral monocytes, few overlapping genes were not enriched in biological processes. Taken together, the identified conditional fear stress-induced changes in mouse microglial transcription profiles suggest that microglia-neuron communication mediates contextual fear conditioning. •Synapse-related genes in microglia are changed by contextual fear conditioning.•Consolidation of fear memory induces immune dysfunction in microglia.•Microglial GABRB3 and Synapsin are changed during contextual fear conditioning.•Transcriptional profiles in microglia are different from the peripheral monocytes.</abstract><pub>Elsevier Inc</pub><doi>10.1016/j.brainresbull.2022.08.017</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0361-9230
ispartof Brain research bulletin, 2022-10, Vol.189, p.57-68
issn 0361-9230
1873-2747
language eng
recordid cdi_proquest_miscellaneous_2704868859
source ScienceDirect Freedom Collection
subjects Fear memory
Microarray
Microglia
Synapsin
γ-aminobutyric acid (GABA)
title Contextual fear conditioning regulates synapse-related gene transcription in mouse microglia
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T19%3A11%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Contextual%20fear%20conditioning%20regulates%20synapse-related%20gene%20transcription%20in%20mouse%20microglia&rft.jtitle=Brain%20research%20bulletin&rft.au=Yu,%20Zhiqian&rft.date=2022-10-15&rft.volume=189&rft.spage=57&rft.epage=68&rft.pages=57-68&rft.issn=0361-9230&rft.eissn=1873-2747&rft_id=info:doi/10.1016/j.brainresbull.2022.08.017&rft_dat=%3Cproquest_cross%3E2704868859%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c475t-dce22a06a9132cda67eda4acf391c8f15c8ef50e0e074b088e4f56de7132e1c13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2704868859&rft_id=info:pmid/&rfr_iscdi=true