Summary: Differences in serotonergic neuron morphology, along with altered gene expression have been identified in patients with MDD. The findings shed light on why some patients do not respond to SSRI antidepressants.
Source: Salk Institute
Selective serotonin reuptake inhibitors (SSRIs) are the most commonly prescribed medication for major depressive disorder (MDD), yet scientists still do not understand why the treatment does not work in nearly thirty percent of patients with MDD. Now, Salk Institute researchers have discovered differences in growth patterns of neurons of SSRI-resistant patients. The work, published in Molecular Psychiatry on March 22, 2019, has implications for depression as well as other psychiatric conditions such as bipolar disorder and schizophrenia that likely also involve abnormalities of the serotonin system in the brain.
“With each new study, we move closer to a fuller understanding of the complex neural circuitry underlying neuropsychiatric diseases, including major depression,” says Salk Professor Rusty Gage, the study’s senior author, president of the Institute, and the Vi and John Adler Chair for Research on Age-Related Neurodegenerative Disease. “This paper, along with another we recently published, not only provides insights into this common treatment but also suggests that other drugs, such as serotonergic antagonists, could be additional options for some patients.”
The cause of depression is still unknown, but scientists believe the disease is partly linked to the serotonergic circuit in the brain. This is largely because SSRIs, which increase levels of the neurotransmitter serotonin at neuron connections, help alleviate the symptoms of many people diagnosed with depression. Yet, the mechanism of why some people respond to SSRIs, while others do not, remains a mystery. Unraveling the puzzle of SSRI resistance has been challenging because it requires studying the 300,000 neurons that use the neurotransmitter serotonin for communication within a brain of 100 billion total neurons. One way scientists have recently overcome this obstacle is to generate these serotonergic neurons in the lab.
The team’s previous paper in Molecular Psychiatry showed that SSRI non-responders had increased receptors for serotonin, which made the neurons hyperactive in response to serotonin. The current paper wanted to examine SSRI non-responders from a different angle.
“We wanted to know if serotonin biochemistry, gene expression, and circuitry were altered in SSRI non-responders compared to responders using serotonergic neurons derived from MDD patients,” says Krishna Vadodaria, a Salk staff scientist and first author of the new paper. “Using neurons derived from actual MDD patients provides a novel representation of how SSRI responders compare to non-responders.”
From a large-scale clinical study of 800 MDD patients, the researchers selected the most extreme cases of SSRI response–patients who drastically improved when taking SSRIs, and patients who saw no effect. The team took skin samples from these patients and reprogrammed the cells into induced pluripotent stem cells (iPSCs) in order to create serotonergic neurons that they could study.
The scientists examined serotonin targets in patient serotonergic neurons, including the enzyme that makes serotonin, the protein that transports it, and the enzyme that breaks it down, but found no differences in biochemistry interactions between groups. Instead, the researchers observed a difference in how the neurons responded based on their shape.
Neurons from SSRI non-responders had longer neuron projections than responders. Gene analysis revealed that the SSRI non-responders also had low levels of key genes (protocadherins PCDHA6 and PCDHA8) involved in forming neuronal circuits. When these genes were made non-functional in serotonergic neurons (mimicking the low gene levels previously observed), the neurons developed the same unusually long projections in the SSRI non-responders. These abnormal features could lead to too much neuronal communication in some areas of the brain and not enough in other parts, altering communication within the serotonergic circuitry and explaining why SSRIs do not always work to treat MDD.
“These results contribute to a new way of examining, understanding, and addressing depression,” says Gage.
The next step is to examine the protocadherin genes to better understand the genetics of SSRI non-responders.
Funding: This work was funded by the Robert and Mary Jane Engman Foundation, Lynn and Edward Streim, a Takeda-Sanford Consortium Innovation Alliance grant program (Takeda Pharmaceutical Company), the Swiss National Science Foundation (SNSF), the Minnesota Partnership Award for Biotechnology and Medical Genomics, the Mayo Clinic Center for Regenerative Medicine, the NIH-Mayo Clinic KL2 Mentored Career Development Award (NCAT UL1TR000135), the Gerstner Family Mayo Career Development Award in Individualized Medicine, and the National Institutes of Health (GM61388 PGRN and RO1 GM28157).
About this neuroscience research article
Source: Salk Institute Media Contacts: Rusty Gage – Salk Institute Image Source: The image is credited to Salk Institute.
Altered serotonergic circuitry in SSRI-resistant major depressive disorder patient-derived neurons
Disrupted serotonergic neurotransmission has long been implicated in major depressive disorder (MDD), for which selective serotonin reuptake inhibitors (SSRIs) are the first line of treatment. However, a significant percentage of patients remain SSRI-resistant and it is unclear whether and how alterations in serotonergic neurons contribute to SSRI resistance in these patients. Induced pluripotent stem cells (iPSCs) facilitate the study of patient-specific neural subtypes that are typically inaccessible in living patients, enabling the discovery of disease-related phenotypes. In our study of a well-characterized cohort of over 800 MDD patients, we generated iPSCs and serotonergic neurons from three extreme SSRI-remitters (R) and SSRI-nonremitters (NR). We studied serotonin (5-HT) biochemistry and observed no significant differences in 5-HT release and reuptake or in genes related to 5-HT biochemistry. NR patient-derived serotonergic neurons exhibited altered neurite growth and morphology downstream of lowered expression of key Protocadherin alpha genes as compared to healthy controls and Rs. Furthermore, knockdown of Protocadherin alpha genes directly regulated iPSC-derived neurite length and morphology. Our results suggest that intrinsic differences in serotonergic neuron morphology and the resulting circuitry may contribute to SSRI resistance in MDD patients.