1. Academic Validation
  2. Hippocampal SGK1 promotes vulnerability to depression: the role of early life adversity, stress, and genetic risk

Hippocampal SGK1 promotes vulnerability to depression: the role of early life adversity, stress, and genetic risk

  • Mol Psychiatry. 2025 Oct 1. doi: 10.1038/s41380-025-03269-6.
Amira Millette 1 Milenna T van Dijk 2 Irina Pokhvisneva 3 Yifei Li 1 Rory Thompson 1 Sachin Patel 3 Rosemary C Bagot 3 4 Aniko Naray-Fejes-Toth 5 Geza Fejes-Toth 5 Patricia Pelufo Silveira 3 Gustavo Turecki 6 Juan Pablo Lopez 7 Christoph Anacker 8 9 10
Affiliations

Affiliations

  • 1 Division of Systems Neuroscience, Research Foundation for Mental Hygiene, Inc., (RFMH) / New York State Psychiatric Institute (NYSPI), Department of Psychiatry, Columbia University Irving Medical Center (CUIMC), New York, NY, 10032, USA.
  • 2 Division of Translational Epidemiology and Mental Health Equity, Research Foundation for Mental Hygiene, Inc., (RFMH) / New York State Psychiatric Institute (NYSPI), Department of Psychiatry, Columbia University Irving Medical Center (CUIMC), New York, NY, 10032, USA.
  • 3 Ludmer Centre for Neuroinformatics and Mental Health, Douglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, QC, Canada.
  • 4 Department of Psychology, McGill University, Montreal, QC, Canada.
  • 5 Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 03755, USA.
  • 6 McGill Group for Suicide Studies, Douglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, QC, Canada.
  • 7 Department of Neuroscience, Karolinska Institutet, Stockholm, 17165, Sweden.
  • 8 Division of Systems Neuroscience, Research Foundation for Mental Hygiene, Inc., (RFMH) / New York State Psychiatric Institute (NYSPI), Department of Psychiatry, Columbia University Irving Medical Center (CUIMC), New York, NY, 10032, USA. ca2635@cumc.columbia.edu.
  • 9 Division of Developmental Neuroscience, Research Foundation for Mental Hygiene, Inc., (RFMH) / New York State Psychiatric Institute (NYSPI), Department of Psychiatry, Columbia University Irving Medical Center (CUIMC), New York, NY, 10032, USA. ca2635@cumc.columbia.edu.
  • 10 Columbia University Stem Cell Initiative (CSCI), Columbia University Irving Medical Center (CUIMC), New York, NY, 10032, USA. ca2635@cumc.columbia.edu.
Abstract

Serum and Glucocorticoid-regulated Kinase 1 (SGK1) is elevated in hippocampal neurons following glucocorticoid exposure and in peripheral blood of depressed patients. However, its mechanistic role in psychopathology and its relevance to the human brain are unknown. To address this gap, we investigated human postmortem brain tissue and found higher SGK1 expression in the hippocampus of depressed suicide decedents compared to healthy subjects who died of natural causes. We observed the highest levels of SGK1 in subjects with reported early life adversity (ELA) - a major risk factor for psychiatric disorders. To determine potential genetic factors underlying increased SGK1 in the hippocampus, we computed expression-based polygenic risk scores (ePRS) for a large population sample from the ABCD study and found that a collection of genetic variants associated with high hippocampal SGK1 expression predicts depression severity and moderates associations between ELA, depressive symptoms, and suicide attempts. Similar to the human brain, hippocampal SGK1 expression was increased in mouse models of ELA, adult chronic stress, and chronic corticosterone exposure, and hippocampal-specific knockdown of SGK1 conferred resilience to stress-induced behavior abnormalities. To test SGK1 as a potential therapeutic target, we injected mice with the small molecule inhibitor, GSK650394, and found that pharmacological inhibition conferred stress resilience, increased adult hippocampal neurogenesis, and rescued stress-induced dentate gyrus hyperactivity. Our cross-species findings reveal a novel role for hippocampal SGK1 in stress resilience, highlight an interaction between ELA and SGK1 on depression and suicide risk, and establish for the first time a functional role for SGK1 in stress-induced psychopathology.

Figures
Products