Retrieval of contextual memory can be predicted by CA3 remapping and is differentially influenced by NMDAR activity in rat hippocampus subregions.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
Magdalena Miranda, Azul Silva, Juan Facundo Morici, Marcos Antonio Coletti, Mariano Belluscio, Pedro Bekinschtein
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引用次数: 0

Abstract

Episodic memory is essential to navigate in a changing environment by recalling past events, creating new memories, and updating stored information from experience. Although the mechanisms for acquisition and consolidation have been profoundly studied, much less is known about memory retrieval. Hippocampal spatial representations are key for retrieval of contextually guided episodic memories. Indeed, hippocampal place cells exhibit stable location-specific activity which is thought to support contextual memory, but can also undergo remapping in response to environmental changes. It is unclear if remapping is directly related to the expression of different episodic memories. Here, using an incidental memory recognition task in rats, we showed that retrieval of a contextually guided memory is reflected by the levels of CA3 remapping, demonstrating a clear link between external cues, hippocampal remapping, and episodic memory retrieval that guides behavior. Furthermore, we describe NMDARs as key players in regulating the balance between retrieval and memory differentiation processes by controlling the reactivation of specific memory traces. While an increase in CA3 NMDAR activity boosts memory retrieval, dentate gyrus NMDAR activity enhances memory differentiation. Our results contribute to understanding how the hippocampal circuit sustains a flexible balance between memory formation and retrieval depending on the environmental cues and the internal representations of the individual. They also provide new insights into the molecular mechanisms underlying the contributions of hippocampal subregions to generate this balance.

通过 CA3 重映射可预测情境记忆的检索,大鼠海马亚区的 NMDAR 活性对情境记忆的检索有不同的影响。
外显记忆对于在不断变化的环境中通过回忆过去的事件、创建新的记忆和更新经验中存储的信息进行导航至关重要。尽管人们对记忆的获得和巩固机制进行了深入研究,但对记忆的检索却知之甚少。海马空间表征是检索情境引导的外显记忆的关键。事实上,海马位置细胞表现出稳定的位置特异性活动,这被认为是对情境记忆的支持,但也会随着环境的变化而发生重映射。目前还不清楚重映射是否与不同情节记忆的表达直接相关。在这里,我们利用大鼠的偶然记忆识别任务表明,情境引导记忆的检索反映了 CA3 重映射的水平,证明了外部线索、海马重映射和引导行为的外显记忆检索之间的明确联系。此外,我们还将 NMDARs 描述为通过控制特定记忆痕迹的重新激活来调节检索和记忆分化过程之间平衡的关键角色。CA3 NMDAR 活性的增加会促进记忆检索,而齿状回 NMDAR 活性的增加则会增强记忆分化。我们的研究结果有助于理解海马回路如何根据环境线索和个体的内部表征在记忆形成和记忆检索之间保持灵活的平衡。这些结果还为我们提供了新的视角,帮助我们了解海马亚区对产生这种平衡所起作用的分子机制。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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