Ketamine induces synaptic and monoaminergic remodeling in human iPSC-derived neurons
Abstract
Major depressive disorder (MDD) is a leading cause of global disability, and a substantial proportion of patients develop treatment-resistant depression (TRD), highlighting the urgent need for mechanistically novel and fast-acting antidepressants. Ketamine has emerged as a paradigm-shifting therapy due to its rapid and robust antidepressant effects, yet its molecular mechanisms in human neurons remain incompletely understood. Here, we investigated the cellular and transcriptomic effects of ketamine in human induced pluripotent stem cell (hiPSC)-derived forebrain neurons. Neuronal cultures were treated with ketamine (1 µM) for 72 h and analyzed using immunocytochemistry, western blotting, and RNA sequencing. Ketamine treatment did not alter gross neuronal morphology or presynaptic organization but significantly increased synaptic localization of the postsynaptic scaffolding protein PSD-95, suggesting molecular changes associated with synaptic remodeling. At the signaling level, ketamine selectively modulated the Akt pathway without inducing changes in BDNF protein levels or MAPK activation, and without broadly altering excitatory or inhibitory synaptic protein expression. Transcriptomic profiling revealed 604 differentially expressed genes, with significant enrichment of pathways related to serotonergic and dopaminergic neurotransmission. Notably, ketamine upregulated genes involved in monoamine synthesis and signaling, including DDC and DRD1 , while downregulating genes associated with GPCR ligand binding and neurotransmitter transport. SynGO analysis further identified selective regulation of synapse-associated genes, predominantly affecting presynaptic and neurotransmitter uptake mechanisms. Together, these findings indicate that ketamine induces molecular and transcriptional changes in human neurons that are consistent with synaptic remodeling and with activation of transcriptional programs enriched for monoaminergic signaling pathways. This hiPSC-based model provides a platform to investigate the molecular responses of human neurons to ketamine and to explore patient-specific mechanisms in future studies.
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BibTeX
@article{pagano2026ketamine,
title = {{Ketamine induces synaptic and monoaminergic remodeling in human iPSC-derived neurons}},
author = {Jessica Pagano and Eleonora Mangano and Sofia Eminente and Matteo Marcatili and Michaela Krivosova and Matteo Colombo and Viviana Tritto and Roberta Bordoni and Tobias M. Boeckers and Luciano Conti and Carlo Sala},
journal = {Translational Psychiatry},
year = {2026},
month = oct,
doi = {10.1038/s41398-026-04525-1},
url = {https://www.nature.com/articles/s41398-026-04525-1},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Ketamine induces synaptic and monoaminergic remodeling in human iPSC-derived neurons
AU - Jessica Pagano
AU - Eleonora Mangano
AU - Sofia Eminente
AU - Matteo Marcatili
AU - Michaela Krivosova
AU - Matteo Colombo
AU - Viviana Tritto
AU - Roberta Bordoni
AU - Tobias M. Boeckers
AU - Luciano Conti
AU - Carlo Sala
PY - 2026
DA - 2026/10/16
JO - Translational Psychiatry
DO - 10.1038/s41398-026-04525-1
UR - https://www.nature.com/articles/s41398-026-04525-1
AB - Major depressive disorder (MDD) is a leading cause of global disability, and a substantial proportion of patients develop treatment-resistant depression (TRD), highlighting the urgent need for mechanistically novel and fast-acting antidepressants. Ketamine has emerged as a paradigm-shifting therapy due to its rapid and robust antidepressant effects, yet its molecular mechanisms in human neurons remain incompletely understood. Here, we investigated the cellular and transcriptomic effects of ketamine in human induced pluripotent stem cell (hiPSC)-derived forebrain neurons. Neuronal cultures were treated with ketamine (1 µM) for 72 h and analyzed using immunocytochemistry, western blotting, and RNA sequencing. Ketamine treatment did not alter gross neuronal morphology or presynaptic organization but significantly increased synaptic localization of the postsynaptic scaffolding protein PSD-95, suggesting molecular changes associated with synaptic remodeling. At the signaling level, ketamine selectively modulated the Akt pathway without inducing changes in BDNF protein levels or MAPK activation, and without broadly altering excitatory or inhibitory synaptic protein expression. Transcriptomic profiling revealed 604 differentially expressed genes, with significant enrichment of pathways related to serotonergic and dopaminergic neurotransmission. Notably, ketamine upregulated genes involved in monoamine synthesis and signaling, including DDC and DRD1 , while downregulating genes associated with GPCR ligand binding and neurotransmitter transport. SynGO analysis further identified selective regulation of synapse-associated genes, predominantly affecting presynaptic and neurotransmitter uptake mechanisms. Together, these findings indicate that ketamine induces molecular and transcriptional changes in human neurons that are consistent with synaptic remodeling and with activation of transcriptional programs enriched for monoaminergic signaling pathways. This hiPSC-based model provides a platform to investigate the molecular responses of human neurons to ketamine and to explore patient-specific mechanisms in future studies.
SN - 2158-3188
ER -