An anti-amyloidogenic approach to specifically block memory consolidation in mice for therapeutic intervention

Lopez-Garcia, P.; McGreevy, K. R.; Vaquero, M. E.; Ramirez de Mingo, D.; Palle, A.; Popiel, H. A.; Santi, A.; Nagai, Y.; Trejo, J. L.; Carrion-Vazquez, M.

doi:10.1101/2025.01.27.635080

bioRxiv · 10.1101/2025.01.27.635080

An anti-amyloidogenic approach to specifically block memory consolidation in mice for therapeutic intervention

Lopez-Garcia, P.·McGreevy, K. R.·Vaquero, M. E.·Ramirez de Mingo, D.·Palle, A.·Popiel, H. A.·Santi, A.·Nagai, Y.·Trejo, J. L.·Carrion-Vazquez, M.

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Abstract

Post-traumatic stress disorder (PTSD) is a mental health disorder triggered by the exposure to a traumatic event, which manifests with anguish, intrusive memories, and negative mood changes. So far, there is no efficient treatment for PTSD other than symptomatic palliative care. However, the cytoplasmic polyadenylation element binding protein-3 (CPEB3) has been recently associated to a potential risk gene for PTSD. Considering that CPEB3 protein is a functional amyloid whose importance for long-term memory consolidation in mammals is well established, we propose the active (amyloid) state of CPEB3 as a promising therapeutic target to block the consolidation of traumatic memories through by the anti-amyloidogenic polyglutamine binding peptide 1 (QBP1). Here we report a preclinical development in mice of this pharmacological treatment for PTSD based on the action of the QBP1 peptide. We first characterized the human CPEB3 (hCPEB3) protein in vitro, showing how its amyloid aggregation is inhibited by the active core of QBP1 (QBP1-M8) without affecting other self-assembly processes such as phase separation. Then, we generated and characterized a novel transgenic mouse that constitutively expresses QBP1 in tandem (TgQBP1). TgQBP1 mice have shown that the consolidation of simple learning is impaired after 24 h for both hippocampal-dependent and aversive memories and that it is limited to new learned memories and has no effect on short-term memory. Furthermore, fear induced anxiety was reduced in comparison to WT mice, suggesting that PTSD-like symptoms are also being ameliorated. Intriguingly, we found that aversive memories seem to be more strongly affected in younger mice. Finally, the analysis of CPEB3 amyloid presence in hippocampal extracted samples showed a correlative decrease in murine CPEB3 oligomerization in the TgQBP1 mice. Taking together, these results strongly suggest that the amyloidogenic blockage of CPEB3 by QBP1 peptide is a potential drug for the prevention and treatment of PTSD.

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Lopez-Garcia, P., McGreevy, K. R., Vaquero, M. E., Ramirez de Mingo, D., Palle, A., Popiel, H. A., Santi, A., Nagai, Y., Trejo, J. L., Carrion-Vazquez, M.. 2025-01-28. An anti-amyloidogenic approach to specifically block memory consolidation in mice for therapeutic intervention. https://doi.org/10.1101/2025.01.27.635080

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