Aggression in male mice depends on developmental estrogen exposure, yet the neural mechanisms underlying this phenomenon remain poorly understood. Although estrogen receptor α (Esr1) has served as a genetic marker to identify aggression-regulating neurons in the ventrolateral division of ventromedial hypothalamus (VMHvl), its functional role in organizing male-aggression circuits remains poorly understood. Here, we developed a genetic strategy to knock out Esr1 in VMHvl neurons while simultaneous tracing and manipulating Esr1-deleted cells. Developmental Esr1 knockout selectively altered synaptic inputs from aggression-regulating regions onto VMHvl neurons, with a stronger effect observed in males, revealing the posterior intralaminar thalamic nucleus (PIL) as a critical upstream region involved in male aggression. Additionally, VMHvl Esr1+ neurons in knockout males showed reduced excitability and failed to initiate attacks upon chemogenetic activation. These findings underscore the essential role of Esr1 in establishing male-specific aggression circuits, providing new insights into male-specific neural circuit development and function.
Keywords: Esr1; VMHvl; aggression circuit; developmental critical period; estrogen; hypothalamus; neural circuit formation; neuronal excitability; sex differences; the posterior intralaminar thalamic nucleus.
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