Neuronal Subtypes and Connectivity of the Adult Mouse Paralaminar Amygdala.
David SaxonPia J AldermanShawn F SorrellsStefano ViciniJoshua G CorbinPublished in: eNeuro (2024)
The paralaminar nucleus of the amygdala (PL) comprises neurons that exhibit delayed maturation. PL neurons are born during gestation but mature during adolescent ages, differentiating into excitatory neurons. These late-maturing PL neurons contribute to the increase in size and cell number of the amygdala between birth and adulthood. However, the function of the PL upon maturation is unknown, as the region has only recently begun to be characterized in detail. In this study, we investigated key defining features of the adult mouse PL; the intrinsic morpho-electric properties of its neurons, and its input and output circuit connectivity. We identify two subtypes of excitatory neurons in the PL based on unsupervised clustering of electrophysiological properties. These subtypes are defined by differential action potential firing properties and dendritic architecture, suggesting divergent functional roles. We further uncover major axonal inputs to the adult PL from the main olfactory network and basolateral amygdala. We also find that axonal outputs from the PL project reciprocally to these inputs and to diverse targets including the amygdala, frontal cortex, hippocampus, hypothalamus, and brainstem. Thus, the adult mouse PL is centrally placed to play a major role in the integration of olfactory sensory information, to coordinate affective and autonomic behavioral responses to salient odor stimuli.
Keyphrases
- functional connectivity
- resting state
- spinal cord
- prefrontal cortex
- spinal cord injury
- childhood cancer
- young adults
- single cell
- mental health
- machine learning
- temporal lobe epilepsy
- preterm infants
- bipolar disorder
- stem cells
- depressive symptoms
- high resolution
- white matter
- rna seq
- mesenchymal stem cells
- blood brain barrier
- working memory
- magnetic resonance
- risk assessment
- subarachnoid hemorrhage
- low birth weight
- cerebral ischemia
- single molecule
- pregnancy outcomes
- high speed