4.8 Article

Serotonin-induced hyperactivity in SSRI-resistant major depressive disorder patient-derived neurons

Journal

MOLECULAR PSYCHIATRY
Volume 24, Issue 6, Pages 795-807

Publisher

SPRINGERNATURE
DOI: 10.1038/s41380-019-0363-y

Keywords

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Funding

  1. Robert and Mary Jane Engman Foundation
  2. Takeda-Sanford Consortium Innovation Alliance grant program (Takeda Pharmaceutical Company)
  3. Swiss National Science Foundation (SNSF) outgoing postdoctoral fellowship
  4. Minnesota Partnership Award for Biotechnology and Medical Genomics
  5. Mayo Clinic Center for Regenerative Medicine
  6. NIH-Mayo Clinic KL2 Mentored Career Development Award [NCAT UL1TR000135]
  7. Gerstner Family Mayo Career Development Award in Individualized Medicine
  8. NIH [RO1 GM28157, U19 GM61388]
  9. Mayo Clinic NIH-PGRN [U19 GM61388]
  10. [NCI P30 CA014195]

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Selective serotonin reuptake inhibitors (SSRIs) are the most prescribed antidepressants. They regulate serotonergic neurotransmission, but it remains unclear how altered serotonergic neurotransmission may contribute to the SSRI resistance observed in approximately 30% of major depressive disorder (MDD) patients. Patient stratification based on pharmacological responsiveness and the use of patient-derived neurons may make possible the discovery of disease-relevant neural phenotypes. In our study from a large cohort of well-characterized MDD patients, we have generated induced pluripotent stem cells (iPSCs) from SSRI-remitters and SSRI-nonremitters. We studied serotonergic neurotransmission in patient forebrain neurons in vitro and observed that nonremitter patient-derived neurons displayed serotonin-induced hyperactivity downstream of upregulated excitatory serotonergic receptors, in contrast to what is seen in healthy and remitter patient-derived neurons. Our data suggest that postsynaptic forebrain hyperactivity downstream of SSRI treatment may play a role in SSRI resistance in MDD.

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