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Sleep-dependent engram reactivation during hippocampal memory consolidation associated with subregion-specific biosynthetic changes.


ABSTRACT: Post-learning sleep is essential for hippocampal memory processing, including contextual fear memory consolidation. We labeled context-encoding engram neurons in the hippocampal dentate gyrus (DG) and assessed reactivation of these neurons after fear learning. Post-learning sleep deprivation (SD) selectively disrupted reactivation of inferior blade DG engram neurons, linked to SD-induced suppression of neuronal activity in the inferior, but not superior DG blade. Subregion-specific spatial profiling of transcripts revealed that transcriptomic responses to SD differed greatly between hippocampal CA1, CA3, and DG inferior blade, superior blade, and hilus. Activity-driven transcripts, and those associated with cytoskeletal remodeling, were selectively suppressed in the inferior blade. Critically, learning-driven transcriptomic changes differed dramatically between the DG blades and were absent from all other regions. Together, these data suggest that the DG is critical for sleep-dependent memory consolidation, and that the effects of sleep loss on the hippocampus are highly subregion-specific.

SUBMITTER: Wang L 

PROVIDER: S-EPMC10957462 | biostudies-literature | 2024 Apr

REPOSITORIES: biostudies-literature

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Sleep-dependent engram reactivation during hippocampal memory consolidation associated with subregion-specific biosynthetic changes.

Wang Lijing L   Park Lauren L   Wu Weisheng W   King Dana D   Vega-Medina Alexis A   Raven Frank F   Martinez Jessy J   Ensing Amy A   McDonald Katherine K   Yang Zhongying Z   Jiang Sha S   Aton Sara J SJ  

iScience 20240304 4


Post-learning sleep is essential for hippocampal memory processing, including contextual fear memory consolidation. We labeled context-encoding engram neurons in the hippocampal dentate gyrus (DG) and assessed reactivation of these neurons after fear learning. Post-learning sleep deprivation (SD) selectively disrupted reactivation of inferior blade DG engram neurons, linked to SD-induced suppression of neuronal activity in the inferior, but not superior DG blade. Subregion-specific spatial profi  ...[more]

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