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Published August 25, 2022 | Supplemental Material + Accepted Version
Journal Article Open

Transformations of neural representations in a social behaviour network

Abstract

Mating and aggression are innate social behaviours that are controlled by subcortical circuits in the extended amygdala and hypothalamus. The bed nucleus of the stria terminalis (BNSTpr) is a node that receives input encoding sex-specific olfactory cues from the medial amygdala, and which in turn projects to hypothalamic nuclei that control mating (medial preoptic area (MPOA)) and aggression (ventromedial hypothalamus, ventrolateral subdivision (VMHvl)), respectively15. Previous studies have demonstrated that male aromatase-positive BNSTpr neurons are required for mounting and attack, and may identify conspecific sex according to their overall level of activity. However, neural representations in BNSTpr, their function and their transformations in the hypothalamus have not been characterized. Here we performed calcium imaging of male BNSTprEsr1 neurons during social behaviours. We identify distinct populations of female- versus male-tuned neurons in BNSTpr, with the former outnumbering the latter by around two to one, similar to the medial amygdala and MPOA but opposite to VMHvl, in which male-tuned neurons predominate. Chemogenetic silencing of BNSTpr^(Esr1) neurons while imaging MPOA^(Esr1) or VMHvl^(Esr1) neurons in behaving animals showed, unexpectedly, that the male-dominant sex-tuning bias in VMHvl was inverted to female-dominant whereas a switch from sniff- to mount-selective neurons during mating was attenuated in MPOA. Our data also indicate that BNSTpr^(Esr1) neurons are not essential for conspecific sex identification. Rather, they control the transition from appetitive to consummatory phases of male social behaviours by shaping sex- and behaviour-specific neural representations in the hypothalamus.

Additional Information

© 2022 Springer Nature. Received 26 March 2021. Accepted 29 June 2022. Published 03 August 2022. We thank A. Kennedy and A. Nair for advice on miniscope data analysis; M. Hui and C. Kim for assistance with animal surgery and behaviour experiments; M. Zelikowsky for advice on statistical analysis; W. Hong for pilot experiments performed on BNSTpr; X. Da, J. Chang and X. Wang for histology; Y. Huang for genotyping; Caltech OLAR staff for animal care; J. Costanza for mouse colony management; M. Schnitzer, A. Vinograd and B. Weissbourd for constructive comments on the manuscript; C. Chiu for laboratory management; G. Mancuso for administrative assistance; and members of the Anderson laboratory for helpful comments on this project. This paper was supported by NIH grant nos. MH070053, MH112593 and NS123916 and by the Simons Collaboration on the Global Brain. D.J.A. is an investigator of the Howard Hughes Medical Institute. Contributions. B.Y. performed experiments, analysed data and prepared figures. T.K. performed retrograde tracing experiments. B.Y. and D.J.A. designed the study and wrote the paper. Data availability. The data on which this study is based are available on reasonable request. Code availability. The custom MATLAB and Python codes used to analyse the data in this study are available on request. Reporting summary. Further information on research design is available in the Nature Research Reporting Summary linked to this paper. The authors declare no competing interests. Peer review information. Nature thanks the anonymous reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.

Attached Files

Accepted Version - nihms-1832469.pdf

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Additional details

Created:
August 22, 2023
Modified:
December 22, 2023