TY - JOUR
T1 - A hypothalamic circuit underlying the dynamic control of social homeostasis
AU - Liu, Ding
AU - Rahman, Mostafizur
AU - Johnson, Autumn
AU - Amo, Ryunosuke
AU - Tsutsui-Kimura, Iku
AU - Sullivan, Zuri A.
AU - Pena, Nicolai
AU - Talay, Mustafa
AU - Logeman, Brandon L.
AU - Finkbeiner, Samantha
AU - Qian, Lechen
AU - Choi, Seungwon
AU - Capo-Battaglia, Athena
AU - Abdus-Saboor, Ishmail
AU - Ginty, David D.
AU - Uchida, Naoshige
AU - Watabe-Uchida, Mitsuko
AU - Dulac, Catherine
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/4/24
Y1 - 2025/4/24
N2 - Social grouping increases survival in many species, including humans1,2. By contrast, social isolation generates an aversive state (‘loneliness’) that motivates social seeking and heightens social interaction upon reunion3, 4–5. The observed rebound in social interaction triggered by isolation suggests a homeostatic process underlying the control of social need, similar to physiological drives such as hunger, thirst or sleep3,6. In this study, we assessed social responses in several mouse strains, among which FVB/NJ mice emerged as highly, and C57BL/6J mice as moderately, sensitive to social isolation. Using both strains, we uncovered two previously uncharacterized neuronal populations in the hypothalamic preoptic nucleus that are activated during either social isolation or social rebound and orchestrate the behaviour display of social need and social satiety, respectively. We identified direct connectivity between these two populations and with brain areas associated with social behaviour, emotional state, reward and physiological needs and showed that mice require touch to assess the presence of others and fulfil their social need. These data show a brain-wide neural system underlying social homeostasis and provide significant mechanistic insights into the nature and function of circuits controlling instinctive social need and for the understanding of healthy and diseased brain states associated with social context.
AB - Social grouping increases survival in many species, including humans1,2. By contrast, social isolation generates an aversive state (‘loneliness’) that motivates social seeking and heightens social interaction upon reunion3, 4–5. The observed rebound in social interaction triggered by isolation suggests a homeostatic process underlying the control of social need, similar to physiological drives such as hunger, thirst or sleep3,6. In this study, we assessed social responses in several mouse strains, among which FVB/NJ mice emerged as highly, and C57BL/6J mice as moderately, sensitive to social isolation. Using both strains, we uncovered two previously uncharacterized neuronal populations in the hypothalamic preoptic nucleus that are activated during either social isolation or social rebound and orchestrate the behaviour display of social need and social satiety, respectively. We identified direct connectivity between these two populations and with brain areas associated with social behaviour, emotional state, reward and physiological needs and showed that mice require touch to assess the presence of others and fulfil their social need. These data show a brain-wide neural system underlying social homeostasis and provide significant mechanistic insights into the nature and function of circuits controlling instinctive social need and for the understanding of healthy and diseased brain states associated with social context.
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UR - http://www.scopus.com/inward/citedby.url?scp=85218751809&partnerID=8YFLogxK
U2 - 10.1038/s41586-025-08617-8
DO - 10.1038/s41586-025-08617-8
M3 - Article
C2 - 40011768
AN - SCOPUS:85218751809
SN - 0028-0836
VL - 640
SP - 1000
EP - 1010
JO - Nature
JF - Nature
IS - 8060
M1 - 372
ER -