Cargando…

Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish

BACKGROUND: Fear conditioning is a form of learning essential for animal survival and used as a behavioral paradigm to study the mechanisms of learning and memory. In mammals, the amygdala plays a crucial role in fear conditioning. In teleost, the medial zone of the dorsal telencephalon (Dm) has bee...

Descripción completa

Detalles Bibliográficos
Autores principales: Lal, Pradeep, Tanabe, Hideyuki, Suster, Maximiliano L., Ailani, Deepak, Kotani, Yuri, Muto, Akira, Itoh, Mari, Iwasaki, Miki, Wada, Hironori, Yaksi, Emre, Kawakami, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978991/
https://www.ncbi.nlm.nih.gov/pubmed/29690872
http://dx.doi.org/10.1186/s12915-018-0502-y
_version_ 1783327597505019904
author Lal, Pradeep
Tanabe, Hideyuki
Suster, Maximiliano L.
Ailani, Deepak
Kotani, Yuri
Muto, Akira
Itoh, Mari
Iwasaki, Miki
Wada, Hironori
Yaksi, Emre
Kawakami, Koichi
author_facet Lal, Pradeep
Tanabe, Hideyuki
Suster, Maximiliano L.
Ailani, Deepak
Kotani, Yuri
Muto, Akira
Itoh, Mari
Iwasaki, Miki
Wada, Hironori
Yaksi, Emre
Kawakami, Koichi
author_sort Lal, Pradeep
collection PubMed
description BACKGROUND: Fear conditioning is a form of learning essential for animal survival and used as a behavioral paradigm to study the mechanisms of learning and memory. In mammals, the amygdala plays a crucial role in fear conditioning. In teleost, the medial zone of the dorsal telencephalon (Dm) has been postulated to be a homolog of the mammalian amygdala by anatomical and ablation studies, showing a role in conditioned avoidance response. However, the neuronal populations required for a conditioned avoidance response via the Dm have not been functionally or genetically defined. RESULTS: We aimed to identify the neuronal population essential for fear conditioning through a genetic approach in zebrafish. First, we performed large-scale gene trap and enhancer trap screens, and created transgenic fish lines that expressed Gal4FF, an engineered version of the Gal4 transcription activator, in specific regions in the brain. We then crossed these Gal4FF-expressing fish with the effector line carrying the botulinum neurotoxin gene downstream of the Gal4 binding sequence UAS, and analyzed the double transgenic fish for active avoidance fear conditioning. We identified 16 transgenic lines with Gal4FF expression in various brain areas showing reduced performance in avoidance responses. Two of them had Gal4 expression in populations of neurons located in subregions of the Dm, which we named 120A-Dm neurons. Inhibition of the 120A-Dm neurons also caused reduced performance in Pavlovian fear conditioning. The 120A-Dm neurons were mostly glutamatergic and had projections to other brain regions, including the hypothalamus and ventral telencephalon. CONCLUSIONS: Herein, we identified a subpopulation of neurons in the zebrafish Dm essential for fear conditioning. We propose that these are functional equivalents of neurons in the mammalian pallial amygdala, mediating the conditioned stimulus–unconditioned stimulus association. Thus, the study establishes a basis for understanding the evolutionary conservation and diversification of functional neural circuits mediating fear conditioning in vertebrates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0502-y) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5978991
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-59789912018-06-06 Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish Lal, Pradeep Tanabe, Hideyuki Suster, Maximiliano L. Ailani, Deepak Kotani, Yuri Muto, Akira Itoh, Mari Iwasaki, Miki Wada, Hironori Yaksi, Emre Kawakami, Koichi BMC Biol Research Article BACKGROUND: Fear conditioning is a form of learning essential for animal survival and used as a behavioral paradigm to study the mechanisms of learning and memory. In mammals, the amygdala plays a crucial role in fear conditioning. In teleost, the medial zone of the dorsal telencephalon (Dm) has been postulated to be a homolog of the mammalian amygdala by anatomical and ablation studies, showing a role in conditioned avoidance response. However, the neuronal populations required for a conditioned avoidance response via the Dm have not been functionally or genetically defined. RESULTS: We aimed to identify the neuronal population essential for fear conditioning through a genetic approach in zebrafish. First, we performed large-scale gene trap and enhancer trap screens, and created transgenic fish lines that expressed Gal4FF, an engineered version of the Gal4 transcription activator, in specific regions in the brain. We then crossed these Gal4FF-expressing fish with the effector line carrying the botulinum neurotoxin gene downstream of the Gal4 binding sequence UAS, and analyzed the double transgenic fish for active avoidance fear conditioning. We identified 16 transgenic lines with Gal4FF expression in various brain areas showing reduced performance in avoidance responses. Two of them had Gal4 expression in populations of neurons located in subregions of the Dm, which we named 120A-Dm neurons. Inhibition of the 120A-Dm neurons also caused reduced performance in Pavlovian fear conditioning. The 120A-Dm neurons were mostly glutamatergic and had projections to other brain regions, including the hypothalamus and ventral telencephalon. CONCLUSIONS: Herein, we identified a subpopulation of neurons in the zebrafish Dm essential for fear conditioning. We propose that these are functional equivalents of neurons in the mammalian pallial amygdala, mediating the conditioned stimulus–unconditioned stimulus association. Thus, the study establishes a basis for understanding the evolutionary conservation and diversification of functional neural circuits mediating fear conditioning in vertebrates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-018-0502-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-25 /pmc/articles/PMC5978991/ /pubmed/29690872 http://dx.doi.org/10.1186/s12915-018-0502-y Text en © Kawakami et al. 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lal, Pradeep
Tanabe, Hideyuki
Suster, Maximiliano L.
Ailani, Deepak
Kotani, Yuri
Muto, Akira
Itoh, Mari
Iwasaki, Miki
Wada, Hironori
Yaksi, Emre
Kawakami, Koichi
Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish
title Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish
title_full Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish
title_fullStr Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish
title_full_unstemmed Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish
title_short Identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish
title_sort identification of a neuronal population in the telencephalon essential for fear conditioning in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978991/
https://www.ncbi.nlm.nih.gov/pubmed/29690872
http://dx.doi.org/10.1186/s12915-018-0502-y
work_keys_str_mv AT lalpradeep identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT tanabehideyuki identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT sustermaximilianol identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT ailanideepak identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT kotaniyuri identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT mutoakira identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT itohmari identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT iwasakimiki identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT wadahironori identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT yaksiemre identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish
AT kawakamikoichi identificationofaneuronalpopulationinthetelencephalonessentialforfearconditioninginzebrafish