Basolateral Amygdala Astrocytes Are Engaged by the Acquisition and Expression of a Contextual Fear Memory

R. L. Suthard, R. Senne, Michelle D. Buzharsky, Angela Y. Pyo, Kaitlyn E. Dorst, A. H. Diep, Rebecca H. Cole, S. Ramirez
{"title":"Basolateral Amygdala Astrocytes Are Engaged by the Acquisition and Expression of a Contextual Fear Memory","authors":"R. L. Suthard, R. Senne, Michelle D. Buzharsky, Angela Y. Pyo, Kaitlyn E. Dorst, A. H. Diep, Rebecca H. Cole, S. Ramirez","doi":"10.1101/2022.09.11.507456","DOIUrl":null,"url":null,"abstract":"Astrocytes are key cellular regulators within the brain. The basolateral amygdala (BLA) is implicated in fear memory processing, yet most research has entirely focused on neuronal mechanisms, despite a significant body of work implicating astrocytes in learning and memory. In the present study, we used in vivo fiber photometry in C57BL/6J male mice to record from amygdalar astrocytes across fear learning, recall, and three separate periods of extinction. We found that BLA astrocytes robustly responded to foot shock during acquisition, their activity remained remarkably elevated across days in comparison to unshocked control animals, and their increased activity persisted throughout extinction. Further, we found that astrocytes responded to the initiation and termination of freezing bouts during contextual fear conditioning and recall, and this behavior-locked pattern of activity did not persist throughout the extinction sessions. Importantly, astrocytes do not display these changes while exploring a novel context, suggesting that these observations are specific to the original fear-associated environment. Chemogenetic inhibition of fear ensembles in the BLA did not affect freezing behavior or astrocytic calcium dynamics. Overall, our work presents a real-time role for amygdalar astrocytes in fear processing and provides new insight into the emerging role of these cells in cognition and behavior. SIGNIFICANCE STATEMENT We show that basolateral amygdala astrocytes are robustly responsive to negative experiences, like shock, and display changed calcium activity patterns through fear learning and memory. Additionally, astrocytic calcium responses become time locked to the initiation and termination of freezing behavior during fear learning and recall. We find that astrocytes display calcium dynamics unique to a fear-conditioned context, and chemogenetic inhibition of BLA fear ensembles does not have an impact on freezing behavior or calcium dynamics. These findings show that astrocytes play a key real-time role in fear learning and memory.","PeriodicalId":22786,"journal":{"name":"The Journal of Neuroscience","volume":"25 1","pages":"4997 - 5013"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2022.09.11.507456","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Astrocytes are key cellular regulators within the brain. The basolateral amygdala (BLA) is implicated in fear memory processing, yet most research has entirely focused on neuronal mechanisms, despite a significant body of work implicating astrocytes in learning and memory. In the present study, we used in vivo fiber photometry in C57BL/6J male mice to record from amygdalar astrocytes across fear learning, recall, and three separate periods of extinction. We found that BLA astrocytes robustly responded to foot shock during acquisition, their activity remained remarkably elevated across days in comparison to unshocked control animals, and their increased activity persisted throughout extinction. Further, we found that astrocytes responded to the initiation and termination of freezing bouts during contextual fear conditioning and recall, and this behavior-locked pattern of activity did not persist throughout the extinction sessions. Importantly, astrocytes do not display these changes while exploring a novel context, suggesting that these observations are specific to the original fear-associated environment. Chemogenetic inhibition of fear ensembles in the BLA did not affect freezing behavior or astrocytic calcium dynamics. Overall, our work presents a real-time role for amygdalar astrocytes in fear processing and provides new insight into the emerging role of these cells in cognition and behavior. SIGNIFICANCE STATEMENT We show that basolateral amygdala astrocytes are robustly responsive to negative experiences, like shock, and display changed calcium activity patterns through fear learning and memory. Additionally, astrocytic calcium responses become time locked to the initiation and termination of freezing behavior during fear learning and recall. We find that astrocytes display calcium dynamics unique to a fear-conditioned context, and chemogenetic inhibition of BLA fear ensembles does not have an impact on freezing behavior or calcium dynamics. These findings show that astrocytes play a key real-time role in fear learning and memory.
杏仁核基底外侧星形胶质细胞参与情境恐惧记忆的获取和表达
星形胶质细胞是大脑中关键的细胞调节器。基底外侧杏仁核(BLA)与恐惧记忆处理有关,尽管有大量的工作表明星形胶质细胞与学习和记忆有关,但大多数研究都集中在神经元机制上。在本研究中,我们使用体内纤维光度法记录了C57BL/6J雄性小鼠的杏仁核星形胶质细胞在恐惧学习、回忆和三个不同的消退时期的变化。我们发现,BLA星形胶质细胞在获得足部电击时反应强烈,与未受到电击的对照动物相比,它们的活性在数天内保持显著升高,并且在灭绝过程中它们的活性持续增加。此外,我们发现星形胶质细胞在情境恐惧条件反射和回忆过程中对冻结发作的开始和结束作出反应,而这种行为锁定的活动模式在整个消失过程中并不持续。重要的是,星形胶质细胞在探索新环境时不会表现出这些变化,这表明这些观察结果是特定于原始恐惧相关环境的。BLA中恐惧集合的化学发生抑制不影响冻结行为或星形细胞钙动力学。总的来说,我们的工作展示了杏仁核星形胶质细胞在恐惧处理中的实时作用,并为这些细胞在认知和行为中的新兴作用提供了新的见解。我们发现杏仁核基底外侧星形胶质细胞对负面经历(如休克)有强烈的反应,并通过恐惧、学习和记忆显示钙活性模式的改变。此外,星形细胞钙反应在恐惧学习和回忆过程中被冻结行为的开始和终止所锁定。我们发现星形胶质细胞在恐惧条件下表现出独特的钙动力学,BLA恐惧集合的化学发生抑制对冻结行为或钙动力学没有影响。这些发现表明星形胶质细胞在恐惧学习和记忆中起着关键的实时作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信