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Hardwired to attack: Transcriptionally defined amygdala subpopulations play distinct roles in innate social behaviors
Social behaviors are innate and supported by dedicated neural circuits, but it remains unclear whether these circuits are developmentally hardwired or established through social experience. Here, we revealed distinct response patterns and functions in social behavior of medial amygdala (MeA) cells o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055059/ https://www.ncbi.nlm.nih.gov/pubmed/36993508 http://dx.doi.org/10.1101/2023.03.16.532692 |
Sumario: | Social behaviors are innate and supported by dedicated neural circuits, but it remains unclear whether these circuits are developmentally hardwired or established through social experience. Here, we revealed distinct response patterns and functions in social behavior of medial amygdala (MeA) cells originating from two embryonically parcellated developmental lineages. MeA cells in male mice that express the transcription factor Foxp2 (MeA(Foxp2)) are specialized for processing male conspecific cues even before puberty and are essential for adult inter-male aggression. In contrast, MeA cells derived from the Dbx1-lineage (MeA(Dbx1)) respond broadly to social cues and are non-essential for male aggression. Furthermore, MeA(Foxp2) and MeA(Dbx1) cells show differential anatomical and functional connectivity. Altogether, our results support a developmentally hardwired aggression circuit at the level of the MeA and we propose a lineage-based circuit organization by which a cell’s embryonic transcription factor profile determines its social information representation and behavior relevance during adulthood. |
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