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Higher-order interactions between hippocampal CA1 neurons are disrupted in amnestic mice.
Yan, Chen; Mercaldo, Valentina; Jacob, Alexander D; Kramer, Emily; Mocle, Andrew; Ramsaran, Adam I; Tran, Lina; Rashid, Asim J; Park, Sungmo; Insel, Nathan; Redish, A David; Frankland, Paul W; Josselyn, Sheena A.
Afiliación
  • Yan C; Program in Neurosciences & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Mercaldo V; Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada.
  • Jacob AD; DeepMind, London, UK.
  • Kramer E; Program in Neurosciences & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Mocle A; Department of Fundamental Neurosciences, University of Lausanne, Lausanne, Switzerland.
  • Ramsaran AI; Program in Neurosciences & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Tran L; Dept. of Psychology, University of Toronto, Toronto, Ontario, Canada.
  • Rashid AJ; Program in Neurosciences & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Park S; Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada.
  • Insel N; Program in Neurosciences & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Redish AD; Dept. of Physiology, University of Toronto, Toronto, Ontario, Canada.
  • Frankland PW; Program in Neurosciences & Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Josselyn SA; Dept. of Psychology, University of Toronto, Toronto, Ontario, Canada.
Nat Neurosci ; 2024 Jul 19.
Article en En | MEDLINE | ID: mdl-39030342
ABSTRACT
Across systems, higher-order interactions between components govern emergent dynamics. Here we tested whether contextual threat memory retrieval in mice relies on higher-order interactions between dorsal CA1 hippocampal neurons requiring learning-induced dendritic spine plasticity. We compared population-level Ca2+ transients as wild-type mice (with intact learning-induced spine plasticity and memory) and amnestic mice (TgCRND8 mice with high levels of amyloid-ß and deficits in learning-induced spine plasticity and memory) were tested for memory. Using machine-learning classifiers with different capacities to use input data with complex interactions, our findings indicate complex neuronal interactions in the memory representation of wild-type, but not amnestic, mice. Moreover, a peptide that partially restored learning-induced spine plasticity also restored the statistical complexity of the memory representation and memory behavior in Tg mice. These findings provide a previously missing bridge between levels of analysis in memory research, linking receptors, spines, higher-order neuronal dynamics and behavior.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Neurosci Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Neurosci Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Canadá