Evidence map›Paper›PMID 40778693›Full record

ArticleHippocampus2025

Combinative Protein Expression of Immediate Early Genes c-Fos, Arc, and Npas4 Along Aversive and Appetitive Experience-Related Neural Networks.

Mary Arai, Hisayuki Osanai, Chris C Snell, Kaylea E Gawf, Takashi Kitamura, Sachie K Ogawa

Abstract read
In one paragraph

Article in Hippocampus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Mary AraiDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Hisayuki OsanaiDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Chris C SnellDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Kaylea E GawfDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Takashi KitamuraDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0001-5597-859X
Sachie K OgawaDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Funding

Neural circuit mechanisms for experience-dependent observational fearR01MH125916 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI KITAMURA, TAKASHI · 2021 to 2025
$2.7M
Neural circuit mechanisms for temporal association learningR01MH120134 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI KITAMURA, TAKASHI · 2020 to 2024
$2.0M
Neural circuit mechanisms for a mirror-induced self-directed behaviorR01NS138075 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI Takashi Kitamura · 2024 to 2026
$1.5M
Endowed Scholar ProgramJapan-U.S. Brain Research Cooperative Program: FY2023NIMH NIH HHS R01 MH120134NIMH NIH HHS R01MH120134NIMH NIH HHS R01 MH125916NIMH NIH HHS R01MH125916NINDS NIH HHS R01 NS138075NINDS NIH HHS R01NS138075
6 · The paper itself

Abstract

Expression of immediate early genes (IEGs) is critical for memory formation and has been widely used to identify the neural substrate of memory traces, termed memory engram cells. Functions of IEGs have been known to be different depending on their types. However, there is limited knowledge about the extent to which different types of IEGs are selectively or concurrently involved in the formation of memory engram. To address this question, we investigated the combinative expression of c-Fos, Arc, and Npas4 proteins using immunohistochemistry following aversive and rewarding experiences across subregions in the prefrontal cortex (PFC), basolateral amygdala (BLA), hippocampal dentate gyrus (DG), and retrosplenial cortex (RSC). Using an automated cell detection algorithm, we found that expression patterns of c-Fos, Npas4, and Arc varied across different brain areas, with a higher increase of IEG expressing cells in the PFC and posterior BLA than in the DG. The combinative expression patterns, along with their experience-induced changes, also differed across brain areas; the co-expression of IEGs increased in the PFC and BLA following experience, whereas the increase was less pronounced in the DG and RSC. Furthermore, we demonstrate that different area-to-area functional connectivity networks were extracted by different IEGs. These findings provide insights into how different IEGs and their combinations identify engram cells, which will contribute to a deeper understanding of the functional significance of IEG-tagged memory engram cells.

Indexed as

Avoidance LearningBasic Helix-Loop-Helix ProteinsBrainCytoskeletal ProteinsGenes, Immediate-EarlyNerve NetNerve Tissue ProteinsProto-Oncogene Proteins c-fosAnimalsMaleRatsRewardactivity regulated cytoskeletal-associated proteinBasic Helix-Loop-Helix ProteinsCytoskeletal ProteinsNerve Tissue ProteinsNpas4 protein, mouseNpas4 protein, ratProto-Oncogene Proteins c-fosco‐expressioncontext conditioningimmediate early genesimmunohistochemistrymemory engram cell

Identifiers

PMID40778693
PMCPMC12333481

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.