mPFC Synaptosome Proteomics Reveals Novel Pathways and Muscarinic Receptor Changes in a Learned Helplessness Mouse Model
Zuhair I. AbdullaiD, Rolando Garcia-Milian, Ernestine Giahyue, Sofia FertuzinhosiD, Florine ColliniD, Weiwei Wang, TuKiet T. LamiD, Angus Clark NairniD, Marina R. PicciottoiD
Abstract
Stressful events are a leading factor in development of depression. The medial prefrontal cortex (mPFC) is strongly associated with depression etiology and exposure to uncontrollable stressors results in synaptic dysfunction and loss. Learned helplessness is a behavioral paradigm that measures effects of repeated exposure to uncontrollable, inescapable stress on later responses to escapable stress. We therefore performed a proteomic analysis of mPFC synaptosomes in a mouse learned helplessness model to identify molecular changes that could contribute to functional consequences of inescapable stress. Male and female mice were evaluated at baseline and following exposure to escapable or inescapable stress followed by an active avoidance test. Label-free mass spectrometry followed by pathway and protein-protein interaction network analyses identified alterations in signaling pathways involved in energy metabolism, neurotransmitter signaling, and protein shuttling. Furthermore, phosphoproteomics revealed alterations related to synaptic function, neurotransmitter signaling and protein internalization, as well as changes in activity of kinases previously identified as mediators of antidepressant efficacy (GSK3B) and receptor internalization (ADRBK1). We more deeply examined alterations in the Acetylcholine Receptor Signaling Pathway, and identified muscarinic receptor proteins (Chrm1, Chrm2, Chrm4) and key proteins involved in their translocation to and from the membrane. These results identify substantial changes in the mPFC proteome following exposure to inescapable stressors. In addition, mPFC muscarinic cholinergic signaling is well placed to mediate responses to an inescapable stressor. This proteomic study will be useful in guiding studies of human mPFC relevant to depression. Data are available via ProteomeXchange with identifier PXD073765.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 28th percentile
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Acetylcholine signaling in the medial prefrontal cortex mediates the ability to learn an active avoidance response following learned helplessness training
Zuhair I. Abdulla, Yann S. Mineur, … Marina R. Picciotto·NeuropsychopharmacologyPeer-reviewed·Oct 3, 2024
- Glutamatergic adaptation to stress in medial prefrontal cortex underlies risk and resilience for pessimistic beliefs
Jessica A. Cooper, Makiah R. Nuutinen, … Michael Tilghman Treadway·bioRxiv·Jun 3, 2020
- Layer-specific input to medial prefrontal cortex is linked to stress susceptibility
Sabahaddin Taha Solakoğlu, Şefik Evren Erdener, … Emine Eren‐Koçak·Translational PsychiatryPeer-reviewed·Apr 9, 2025
- NPAS4 in the medial prefrontal cortex mediates chronic social defeat stress- induced anhedonia and dendritic spine loss
Brandon W. Hughes, Benjamin M. Siemsen, … Makoto Taniguchi·eLifePeer-reviewed·Jan 30, 2023
- Multi-OMIC analysis of brain and serum from chronically-stressed mice reveals network disruptions in purine metabolism, fatty acid beta-oxidation, and antioxidant activity that are reversed by antidepressant treatment
Peter J. Hamilton, Emily Y. Chen, … Eric J. Nestler·bioRxiv·Dec 8, 2018
- Dynamic behavioral and molecular changes induced by chronic stress exposure in mice
Thomas D. Prévot, Dipashree Chatterjee, … Mounira Banasr·bioRxiv·May 7, 2021