4.4 Article

Cell-type-specific translational control of spatial working memory by the cap-binding protein 4EHP

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MOLECULAR BRAIN
卷 16, 期 1, 页码 -

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BMC
DOI: 10.1186/s13041-023-00995-2

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Glutamatergic neurons; GABAergic neurons; eIF4E homologous protein (4EHP); Mechanistic target of rapamycin complex 1 (mTORC1)

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The consolidation of learned information into long-lasting memories requires the strengthening of synaptic connections through protein synthesis. Translation initiation factors are crucial for regulating memory formation. The role of the translation inhibitor 4EHP in learning and memory was unknown. Conditional knockout mice for 4EHP were generated and behavioral memory tasks were analyzed. The results showed that 4EHP is necessary for working memory, mediated by mTORC1 activity in excitatory and inhibitory neurons.
The consolidation of learned information into long-lasting memories requires the strengthening of synaptic connections through de novo protein synthesis. Translation initiation factors play a cardinal role in gating the production of new proteins thereby regulating memory formation. Both positive and negative regulators of translation play a critical role in learning and memory consolidation. The eukaryotic initiation factor 4E (eIF4E) homologous protein (4EHP, encoded by the gene Eif4e2) is a pivotal negative regulator of translation but its role in learning and memory is unknown. To address this gap in knowledge, we generated excitatory (glutamatergic: CaMKII alpha-positive) and inhibitory (GABAergic: GAD65-positive) conditional knockout mice for 4EHP, which were analyzed in various behavioral memory tasks. Knockout of 4EHP in Camk2a-expressing neurons (4EHP-cKO(exc)) did not impact long-term memory in either contextual fear conditioning or Morris water maze tasks. Similarly, long-term contextual fear memory was not altered in Gad2-directed 4EHP knockout mice (4EHP-cKO(inh)). However, when subjected to a short-term T-maze working memory task, both mouse models exhibited impaired cognition. We therefore tested the hypothesis that de novo protein synthesis plays a direct role in working memory. We discovered that phosphorylation of ribosomal protein S6, a measure of mTORC1 activity, is dramatically reduced in the CA1 hippocampus of 4EHP-cKO(exc) mice. Consistently, genetic reduction of mTORC1 activity in either excitatory or inhibitory neurons was sufficient to impair working memory. Taken together, these findings indicate that translational control by 4EHP and mTORC1 in both excitatory and inhibitory neurons are necessary for working memory.

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