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Updated: Jun 9, 2025
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Published on: April 5, 2016
Translational Insights From Cell Type Variation Across Amygdala Subnuclei in Rhesus Monkeys and Humans
Shawn Kamboj1, Erin L Carlson1, Bradley P Ander1
1Department of Psychology (Kamboj, Fox), California National Primate Research Center (Kamboj, Bauman, Fox), and MIND Institute (Carlson, Ander, Hanson, Bauman, Schumann), University of California, Davis; Department of Psychiatry and Behavioral Sciences (Carlson, Hanson, Schumann), Department of Neurology (Ander), and Department of Physiology and Membrane Biology (Murray, Bauman), School of Medicine, University of California, Davis; Department of Neuroscience and Department of Psychiatry, School of Medicine and Dentistry, University of Rochester, Rochester, NY (Fudge).
Objective:
Theories of amygdala function are central to our understanding of psychiatric and neurodevelopmental disorders. However, limited knowledge of the molecular and cellular composition of the amygdala impedes translational research aimed at developing new treatments and interventions. The aim of this study was to characterize and compare the composition of amygdala cells to help bridge the gap between preclinical models and human psychiatric and neurodevelopmental disorders.
Methods:
Tissue was dissected from multiple amygdala subnuclei in both humans (N=3, male) and rhesus macaques (N=3, male). Single-nucleus RNA sequencing was performed to characterize the transcriptomes of individual nuclei.
Results:
The results reveal substantial heterogeneity between regions, even when restricted to inhibitory or excitatory neurons. Consistent with previous work, the data highlight the complexities of individual marker genes for uniquely targeting specific cell types. Cross-species analyses suggest that the rhesus monkey model is well-suited to understanding the human amygdala, but also identify limitations. For example, a cell cluster in the ventral lateral nucleus of the amygdala (vLa) is enriched in humans relative to rhesus macaques. Additionally, the data describe specific cell clusters with relative enrichment of disorder-related genes. These analyses point to the human-enriched vLa cell cluster as relevant to autism spectrum disorder, potentially highlighting a vulnerability to neurodevelopmental disorders that has emerged in recent primate evolution. Further, a cluster of cells expressing markers for intercalated cells is enriched for genes reported in human genome-wide association studies of neuroticism, anxiety disorders, and depressive disorders.
Conclusions:
Together, these findings shed light on the composition of the amygdala and identify specific cell types that can be prioritized in basic science research to better understand human psychopathology and guide the development of potential treatments.
