Experience alters hippocampal and cortical network communication via a KIBRA-dependent mechanism.
Experience alters hippocampal and cortical network communication via a KIBRA-dependent mechanism.
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DOI:
10.1016/j.celrep.2023.112662
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发表时间:
2023-06-27
期刊:
影响因子:
8.8
通讯作者:
中科院分区:
文献类型:
--
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Synaptic plasticity is hypothesized to underlie “replay” of salient experience during hippocampal sharp-wave/ripple (SWR)-based ensemble activity and to facilitate systems-level memory consolidation coordinated by SWRs and cortical sleep spindles. It remains unclear how molecular changes at synapses contribute to experience-induced modification of network function. The synaptic protein KIBRA regulates plasticity and memory. To determine the impact of KIBRA-regulated plasticity on circuit dynamics, we recorded in vivo neural activity from wild-type (WT) mice and littermates lacking KIBRA and examined circuit function before, during, and after novel experience. In WT mice, experience altered population activity and oscillatory dynamics in a manner consistent with incorporation of new information content in replay and enhanced hippocampal-cortical communication. While baseline SWR features were normal in KIBRA conditional knockout (cKO) mice, experience-dependent alterations in SWRs were absent. Furthermore, intra-hippocampal and hippocampal-cortical communication during SWRs was disrupted following KIBRA deletion. These results indicate molecular mechanisms that underlie network-level adaptations to experience. Hippocampal sharp wave/ripples (SWRs) and cortical spindles are coordinated network oscillations proposed to support memory consolidation. Quigley et al. show that KIBRA, a memory-associated regulator of AMPAR trafficking, is required for experience-induced modification and temporal coupling of SWRs and spindles. They identify plasticity mechanisms that enable networks to adapt to new experience.
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