Connectivity and molecular profiles of Foxp2‐ and Dbx1‐lineage neurons in the accessory olfactory bulb and medial amygdala

Author:

Prakash Nandkishore1ORCID,Matos Heidi Y.1ORCID,Sebaoui Sonia1ORCID,Tsai Luke1ORCID,Tran Tuyen1,Aromolaran Adejimi1,Atrachji Isabella1,Campbell Nya1,Goodrich Meredith1,Hernandez‐Pineda David1,Herrero Maria Jesus1ORCID,Hirata Tsutomu1,Lischinsky Julieta1ORCID,Martinez Wendolin1,Torii Shisui1,Yamashita Satoshi1,Hosseini Hassan2ORCID,Sokolowski Katie1,Esumi Shigeyuki1,Kawasawa Yuka Imamura3ORCID,Hashimoto‐Torii Kazue1,Jones Kevin S.24ORCID,Corbin Joshua G.1ORCID

Affiliation:

1. Center for Neuroscience Research Children's Research Institute, Children's National Hospital Washington District of Columbia USA

2. Department of Pharmacology University of Michigan Medical School Ann Arbor Michigan USA

3. Department of Pharmacology Pennsylvania State University College of Medicine Hershey Pennsylvania USA

4. Neuroscience Graduate Program University of Michigan Medical School Ann Arbor Michigan USA

Abstract

AbstractIn terrestrial vertebrates, the olfactory system is divided into main (MOS) and accessory (AOS) components that process both volatile and nonvolatile cues to generate appropriate behavioral responses. While much is known regarding the molecular diversity of neurons that comprise the MOS, less is known about the AOS. Here, focusing on the vomeronasal organ (VNO), the accessory olfactory bulb (AOB), and the medial amygdala (MeA), we reveal that populations of neurons in the AOS can be molecularly subdivided based on their ongoing or prior expression of the transcription factors Foxp2 or Dbx1, which delineate separate populations of GABAergic output neurons in the MeA. We show that a majority of AOB neurons that project directly to the MeA are of the Foxp2 lineage. Using single‐neuron patch‐clamp electrophysiology, we further reveal that in addition to sex‐specific differences across lineage, the frequency of excitatory input to MeA Dbx1‐ and Foxp2‐lineage neurons differs between sexes. Together, this work uncovers a novel molecular diversity of AOS neurons, and lineage and sex differences in patterns of connectivity.

Publisher

Wiley

Subject

General Neuroscience

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