Short-term social isolation acts on hypothalamic neurons to promote social behavior in a sex- and context-dependent manner

Author:

Zhao Xin1ORCID,Chae Yurim1,Smith Destiny1,Chen Valerie1,DeFelipe Dylan1,Sokol Joshua W1,Sadangi Archana1,Tschida Katherine1ORCID

Affiliation:

1. Department of Psychology, Cornell University

Abstract

Social animals, including both humans and mice, are highly motivated to engage in social interactions. Short-term social isolation increases social motivation and promotes social behavior, but the neural circuits through which it does so remain incompletely understood. Here, we sought to identify neurons that promote social behavior in single-housed female mice, which exhibit increased rates of social investigation, social ultrasonic vocalizations (USVs), and mounting during same-sex interactions that follow a period of short-term (3-day) isolation. We first used immunostaining for the immediate early gene Fos to identify a population of neurons in the preoptic hypothalamus (POA) that increase their activity in single-housed females following same-sex interactions (POA iso neurons). TRAP2-mediated chemogenetic silencing of POA iso neurons in single-housed females significantly attenuates the effects of short-term isolation on social investigation and USV production and also tends to reduce mounting. In contrast, caspase-mediated ablation of POA iso neurons in single-housed females robustly attenuates mounting but has no effect on social investigation or USV production. Optogenetic activation of POA iso neurons in group-housed females promotes USV production but does not recapitulate the effects of short-term isolation on social investigation and mounting. To understand whether a similar population of POA iso neurons promotes social behavior in single-housed males, we performed Fos immunostaining in single-housed males following either same-sex or opposite-sex social interactions. These experiments revealed a population of POA neurons that increase Fos expression in single-housed males following opposite-sex, but not same-sex, interactions.Chemogenetic silencing of POA iso neurons in single-housed males during interactions with females tends to reduce mounting but does not decrease social investigation or USV production. These experiments identify a population of hypothalamic neurons that promote social behavior following short-term isolation in a sex- and social context-dependent manner.

Publisher

eLife Sciences Publications, Ltd

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