Chemogenetic Activation of Astrocytes in the Basolateral Amygdala Contributes to Fear Memory Formation by Modulating the Amygdala-Prefrontal Cortex Communication.

anxiety astrocytes basolateral amygdala chemogenetic electrophysiology fear conditioning medial prefrontal cortex neurons projection

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
29 May 2022
Historique:
received: 28 02 2022
revised: 25 05 2022
accepted: 27 05 2022
entrez: 10 6 2022
pubmed: 11 6 2022
medline: 14 6 2022
Statut: epublish

Résumé

The basolateral amygdala (BLA) is one of the key brain areas involved in aversive learning, especially fear memory formation. Studies of aversive learning in the BLA have largely focused on neuronal function, while the role of BLA astrocytes in aversive learning remains largely unknown. In this study, we manipulated the BLA astrocytes by expressing the Gq-coupled receptor hM3q and discovered that astrocytic Gq modulation during fear conditioning promoted auditorily cued fear memory but did not affect less stressful memory tasks or induce anxiety-like behavior. Moreover, chemogenetic activation of BLA astrocytes during memory retrieval had no effect on fear memory expression. In addition, astrocytic Gq activation increased c-Fos expression in the BLA and the medial prefrontal cortex (mPFC) during fear conditioning, but not in the home cage. Combining these results with retrograde virus tracing, we found that the activity of mPFC-projecting BLA neurons showed significant enhancement after astrocytic Gq activation during fear conditioning. Electrophysiology recordings showed that activating astrocytic Gq in the BLA promoted spike-field coherence and phase locking percentage, not only within the BLA but also between the BLA and the mPFC. Finally, direct chemogenetic activation of mPFC-projecting BLA neurons during fear conditioning enhanced cued fear memory. Taken together, our data suggest that astrocytes in the BLA may contribute to aversive learning by modulating amygdala-mPFC communication.

Identifiants

pubmed: 35682767
pii: ijms23116092
doi: 10.3390/ijms23116092
pmc: PMC9181030
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : General Research Fund, Research Grants Council of Hong Kong
ID : 11103721
Organisme : General Research Fund, Research Grants Council of Hong Kong
ID : 11102820
Organisme : General Research Fund, Research Grants Council of Hong Kong
ID : 11100018
Organisme : National Natural Science Foundation of China (NSFC) and RGC Joint Research Scheme
ID : 3171101014, N_CityU114/17
Organisme : Innovation and Technology Fund Hong Kong
ID : CityU 9445909
Organisme : Shenzhen-Hong Kong Institute of Brain Science Innovation Open Project Contract
ID : NYKFKT2019012
Organisme : City University of Hong Kong Neuroscience Research Infrastructure Grant
ID : 9610211
Organisme : Centre for Biosystems, Neuroscience, and Nanotechnology Grant
ID : 9360148

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Auteurs

Zhuogui Lei (Z)

Department of Neuroscience, City University of Hong Kong, Hong Kong 999077, China.
Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.

Li Xie (L)

Department of Neuroscience, City University of Hong Kong, Hong Kong 999077, China.

Cheuk Hin Li (CH)

Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.

Yuk Yan Lam (YY)

Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.

Aruna Surendran Ramkrishnan (AS)

Department of Neuroscience, City University of Hong Kong, Hong Kong 999077, China.
Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.

Zhongqi Fu (Z)

Department of Neuroscience, City University of Hong Kong, Hong Kong 999077, China.
Centre for Regenerative Medicine and Health, Hong Kong Institute of Science & Innovation, Chinese Academy of Sciences, Hong Kong 999077, China.

Xianlin Zeng (X)

Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.

Shu Liu (S)

Department of Neuroscience, City University of Hong Kong, Hong Kong 999077, China.
Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.

Zafar Iqbal (Z)

Department of Neuroscience, City University of Hong Kong, Hong Kong 999077, China.
Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.

Ying Li (Y)

Department of Neuroscience, City University of Hong Kong, Hong Kong 999077, China.
Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China.
Centre for Regenerative Medicine and Health, Hong Kong Institute of Science & Innovation, Chinese Academy of Sciences, Hong Kong 999077, China.
Centre for Biosystems, Neuroscience, and Nanotechnology, City University of Hong Kong, Hong Kong 999077, China.

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Classifications MeSH