Abstract
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 geneArcfollowing intermale aggression or mating. Here, we sought to better understand howArc-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 labelArc-expressing IGCs following male–male resident–intruder interactions. Using whole-cell patch-clamp electrophysiology, we found thatArc-expressing IGCs display increased intrinsic excitability for several days after a single resident–intruder interaction. Further, we found thatArc-expressing IGCs maintain this increased excitability across repeated resident–intruder interactions, during which resident mice increase or “ramp” their aggression. We tested the hypothesis thatArc-expressing IGCs participate in ramping aggression. Using a combination of ArcTRAP mice and chemogenetics (Cre-dependent hM4D(Gi)-mCherry AAV injections), we found that disruption ofArc-expressing IGC activity during repeated resident–intruder interactions abolishes the ramping aggression exhibited by resident male mice. This work shows thatArc-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 STATEMENTThe 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 geneArcafter the resident–intruder paradigm increase their excitability for several days. We investigated the roles of theseArc-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.
Funder
HHS | NIH | National Institute on Deafness and Other Communication Disorders
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1 articles.
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