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Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity

The accessory olfactory system (AOS) is critical for the development and expression of social behavior. The first dedicated circuit in the AOS, the accessory olfactory bulb (AOB), exhibits cellular and network plasticity in male and female mice after social experience. In the AOB, interneurons calle...

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Autores principales: Zuk, Kelsey E., Cansler, Hillary L., Wang, Jinxin, Meeks, Julian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9962775/
https://www.ncbi.nlm.nih.gov/pubmed/36623874
http://dx.doi.org/10.1523/JNEUROSCI.0847-22.2022
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author Zuk, Kelsey E.
Cansler, Hillary L.
Wang, Jinxin
Meeks, Julian P.
author_facet Zuk, Kelsey E.
Cansler, Hillary L.
Wang, Jinxin
Meeks, Julian P.
author_sort Zuk, Kelsey E.
collection PubMed
description The accessory olfactory system (AOS) is critical for the development and expression of social behavior. The first dedicated circuit in the AOS, the accessory olfactory bulb (AOB), exhibits cellular and network plasticity in male and female mice after social experience. In the AOB, interneurons called internal granule cells (IGCs) express the plasticity-associated immediate-early gene Arc following intermale aggression or mating. Here, we sought to better understand how Arc-expressing IGCs shape AOB information processing and social behavior in the context of territorial aggression. We used “ArcTRAP” (Arc-CreERT2) transgenic mice to selectively and permanently label Arc-expressing IGCs following male–male resident–intruder interactions. Using whole-cell patch-clamp electrophysiology, we found that Arc-expressing IGCs display increased intrinsic excitability for several days after a single resident–intruder interaction. Further, we found that Arc-expressing IGCs maintain this increased excitability across repeated resident–intruder interactions, during which resident mice increase or “ramp” their aggression. We tested the hypothesis that Arc-expressing IGCs participate in ramping aggression. Using a combination of ArcTRAP mice and chemogenetics (Cre-dependent hM4D(G(i))-mCherry AAV injections), we found that disruption of Arc-expressing IGC activity during repeated resident–intruder interactions abolishes the ramping aggression exhibited by resident male mice. This work shows that Arc-expressing AOB IGC ensembles are activated by specific chemosensory environments, and play an integral role in the establishment and expression of sex-typical social behavior. These studies identify a population of plastic interneurons in an early chemosensory circuit that display physiological features consistent with simple memory formation, increasing our understanding of central chemosensory processing and mammalian social behavior. SIGNIFICANCE STATEMENT The accessory olfactory system plays a vital role in rodent chemosensory social behavior. We studied experience-dependent plasticity in the accessory olfactory bulb and found that internal granule cells expressing the immediate-early gene Arc after the resident–intruder paradigm increase their excitability for several days. We investigated the roles of these Arc-expressing internal granule cells on chemosensory social behavior by chemogenetically manipulating their excitability during repeated social interactions. We found that inhibiting these cells eliminated intermale aggressive ramping behavior. These studies identify a population of plastic interneurons in an early chemosensory circuit that display physiological features consistent with simple memory formation, increasing our understanding of central chemosensory processing and mammalian social behavior.
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spelling pubmed-99627752023-02-26 Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity Zuk, Kelsey E. Cansler, Hillary L. Wang, Jinxin Meeks, Julian P. J Neurosci Research Articles The accessory olfactory system (AOS) is critical for the development and expression of social behavior. The first dedicated circuit in the AOS, the accessory olfactory bulb (AOB), exhibits cellular and network plasticity in male and female mice after social experience. In the AOB, interneurons called internal granule cells (IGCs) express the plasticity-associated immediate-early gene Arc following intermale aggression or mating. Here, we sought to better understand how Arc-expressing IGCs shape AOB information processing and social behavior in the context of territorial aggression. We used “ArcTRAP” (Arc-CreERT2) transgenic mice to selectively and permanently label Arc-expressing IGCs following male–male resident–intruder interactions. Using whole-cell patch-clamp electrophysiology, we found that Arc-expressing IGCs display increased intrinsic excitability for several days after a single resident–intruder interaction. Further, we found that Arc-expressing IGCs maintain this increased excitability across repeated resident–intruder interactions, during which resident mice increase or “ramp” their aggression. We tested the hypothesis that Arc-expressing IGCs participate in ramping aggression. Using a combination of ArcTRAP mice and chemogenetics (Cre-dependent hM4D(G(i))-mCherry AAV injections), we found that disruption of Arc-expressing IGC activity during repeated resident–intruder interactions abolishes the ramping aggression exhibited by resident male mice. This work shows that Arc-expressing AOB IGC ensembles are activated by specific chemosensory environments, and play an integral role in the establishment and expression of sex-typical social behavior. These studies identify a population of plastic interneurons in an early chemosensory circuit that display physiological features consistent with simple memory formation, increasing our understanding of central chemosensory processing and mammalian social behavior. SIGNIFICANCE STATEMENT The accessory olfactory system plays a vital role in rodent chemosensory social behavior. We studied experience-dependent plasticity in the accessory olfactory bulb and found that internal granule cells expressing the immediate-early gene Arc after the resident–intruder paradigm increase their excitability for several days. We investigated the roles of these Arc-expressing internal granule cells on chemosensory social behavior by chemogenetically manipulating their excitability during repeated social interactions. We found that inhibiting these cells eliminated intermale aggressive ramping behavior. These studies identify a population of plastic interneurons in an early chemosensory circuit that display physiological features consistent with simple memory formation, increasing our understanding of central chemosensory processing and mammalian social behavior. Society for Neuroscience 2023-02-15 /pmc/articles/PMC9962775/ /pubmed/36623874 http://dx.doi.org/10.1523/JNEUROSCI.0847-22.2022 Text en Copyright © 2023 Zuk et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Zuk, Kelsey E.
Cansler, Hillary L.
Wang, Jinxin
Meeks, Julian P.
Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity
title Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity
title_full Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity
title_fullStr Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity
title_full_unstemmed Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity
title_short Arc-Expressing Accessory Olfactory Bulb Interneurons Support Chemosensory Social Behavioral Plasticity
title_sort arc-expressing accessory olfactory bulb interneurons support chemosensory social behavioral plasticity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9962775/
https://www.ncbi.nlm.nih.gov/pubmed/36623874
http://dx.doi.org/10.1523/JNEUROSCI.0847-22.2022
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