Mechanisms underlying the development, evolution, and function of human-specific cortical dopaminergic interneurons

Active Project Grant Awarded Last action

Award ID
F30MH140382
Recipient
Awarding agency
Obligated
$150,900

Award facts

Assistance listing
93.242 Mental Health Research Grants
Completion date 73% complete
Place of performance
Madison, WI 53715, USA

Award details come from USAspending.gov.

About this award

The National Institute of Mental Health awarded the University of Wisconsin - Madison $150,900 under the Mental Health Research Grants program (CFDA 93.242) on September 17, 2025, to investigate the mechanisms underlying the development, evolution, and function of human-specific cortical dopaminergic interneurons.

The funded research addresses fundamental gaps in understanding a population of inhibitory interneurons in the human cerebral cortex that produce and release dopamine—a capability absent in nonhuman primate species including chimpanzees, bonobos, and gorillas. The investigator will characterize the functional properties of these neurons and identify the developmental and evolutionary mechanisms that explain their selective presence in humans but absence in closely related species. Elucidating the dopaminergic system's molecular, cellular, and physiological underpinnings is intended to support development of novel therapeutic interventions for psychiatric disorders including attention deficit hyperactivity disorder, bipolar disorder, and schizophrenia, which involve dysregulation of dopaminergic neurotransmission.

The period of performance runs through March 31, 2027, with work performed in Madison, Wisconsin.

Description

Abstract
Dopamine is a monoamine neuromodulator that is critical for the regulation of complex behaviors in the human brain. Dysregulation of dopaminergic neurotransmission has been implicated in a spectrum of psychiatric disorders, including attention deficit hyperactivity disorder (adhd), bipolar disorder, and schizophrenia. Moreover, a substantial proportion of psychotropic medications, most notably antipsychotics, exert their therapeutic effects through the modulation of dopamine signaling. Elucidating the molecular, cellular, and physiological underpinnings of the human dopaminergic system will be essential in the development of novel and targeted therapeutic interventions for psychiatric illnesses. Recently, our lab has uncovered a population of inhibitory interneurons in the cerebral cortex that although present in non-human primate species, display unique molecular features in humans. We found that in humans, but not other mammalian species, these interneurons express the key components of dopamine synthesis and are capable of producing and releasing dopamine. Importantly, we identified that dopaminergic interneurons are completely absent from the cerebral cortices of our closest living relatives, the nonhuman african great apes (chimpanzee, bonobo, and gorilla species). These observed differences in the abundance of dopaminergic interneurons between species, along with their distinct molecular profile in the human cortex, suggests a human-specific role for these neurons within neocortical circuits. However, fundamental questions on the development and function of these interneurons remain unanswered. The objective of this proposal is to unravel the functional properties of human cortical dopaminergic interneurons and to identify the developmental and evolutionary mechanisms underlying the selective absence of dopaminergic interneurons in the cerebral cortices of nonhuman african great apes. To accomplish this, we will use human and chimpanzee stem cell-derived brain organoids to model developmental dynamics of brain development and assess the function of dopaminergic interneurons with simultaneous profiling of electrophysiology and transcriptomics in single cells (patch-SEQ). The proposed experiments stand to significantly deepen our mechanistic and physiological understanding of a highly-derived neuronal subtype in the human cerebral cortex. Unraveling the function of cortical dopaminergic interneurons as well as the developmental and evolutionary mechanisms that underlie these functions will provide crucial insights into the human dopaminergic system and identify putative targets for intervention in dopamine-associated psychopathologies. In addition to this research, my training with the university of wisconsin medical scientist training program will provide an exceptional foundation in the technical skills, responsible conduct of research, leadership, and clinical expertise to become a successful independent physician-scientist in child and adolescent psychiatry.

Transactions

Action Obligated Date
Amendment $5,060
Amendment $34,114
Amendment $34,114
Amendment $564
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Amendment $0
Amendment $37,960
Original award $37,960

Quick answers

Who received award F30MH140382?

F30MH140382 was awarded to University Of Wisconsin System by National Institute of Mental Health (National Institutes of Health) on September 17, 2025.

How much is award F30MH140382 worth?

$150,900 has been obligated on F30MH140382.

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