TY - JOUR
T1 - Connectivity and molecular profiles of Foxp2- and Dbx1-lineage neurons in the accessory olfactory bulb and medial amygdala
AU - Prakash, Nandkishore
AU - Matos, Heidi Y.
AU - Sebaoui, Sonia
AU - Tsai, Luke
AU - Tran, Tuyen
AU - Aromolaran, Adejimi
AU - Atrachji, Isabella
AU - Campbell, Nya
AU - Goodrich, Meredith
AU - Hernandez-Pineda, David
AU - Herrero, Maria Jesus
AU - Hirata, Tsutomu
AU - Lischinsky, Julieta
AU - Martinez, Wendolin
AU - Torii, Shisui
AU - Yamashita, Satoshi
AU - Hosseini, Hassan
AU - Sokolowski, Katie
AU - Esumi, Shigeyuki
AU - Kawasawa, Yuka Imamura
AU - Hashimoto-Torii, Kazue
AU - Jones, Kevin S.
AU - Corbin, Joshua G.
N1 - Publisher Copyright:
© 2024 Wiley Periodicals LLC.
PY - 2024/2
Y1 - 2024/2
N2 - In 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.
AB - In 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.
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U2 - 10.1002/cne.25545
DO - 10.1002/cne.25545
M3 - Article
C2 - 37849047
AN - SCOPUS:85174256799
SN - 0021-9967
VL - 532
JO - Journal of Comparative Neurology
JF - Journal of Comparative Neurology
IS - 2
M1 - e25545
ER -