Identifying a functional role for transcriptionally distinct, BLA-activated LS ensembles in social behaviors - Project Summary
Social recognition is the ability to distinguish between novel and familiar conspecifics. This social
behavior is essential for organismal survival as an organism mist be able to direct their behavior based on a
social stimulus or presentation. Recent evidence from our lab has identified that neurons projecting from the
basolateral amygdala (BLA) to the lateral septum (LS) are critically involved in social recognition. However, the
mechanisms governing activation of LS neurons by BLA input are understudied. My long-term goal is to better
understand the neural substrates regulating social behaviors at the circuit, cellular, and molecular levels. The
objective of this project – to study the role of BLA-activated LS neuronal ensembles in regulating social
recognition, and to characterize both the spatial topography and transcriptional heterogeneity of these
ensembles, is the first step toward this long-term goal. Based on previous findings implicating the BLA-LS circuit
in regulating social recognition, my central hypothesis is that activating LS-projecting BLA neurons recruits a
transcriptionally distinct ensemble of LS neurons that are required for social recognition. The rationale for the
proposed research is that identifying a functional role for a specific, molecularly defined LS neuronal
subpopulation in social recognition will provide further understanding of the neural substrates regulating
hardcoded social behaviors essential for organismal survival. The central hypothesis of this proposal will be
tested by pursuing two specific aims: 1) elucidate molecular signatures of BLA-activated LS ensembles across
the spatial topography of the LS, and 2) test the necessity and sufficiency of BLA-activated LS neuronal
ensembles in social recognition. This approach is innovative because it proposes to use circuit-specific, activity-
dependent tagging of neuronal ensembles to both functionally interrogate the population and comprehensively
characterize its molecular signature. The proposed research is significant because it will shed light on the
neurobiological underpinnings that govern the development of social behaviors, and could potentially identify
novel therapeutic targets for the treatment of neurodevelopmental disorders with social deficits.