Evidence map›Paper›PMID 42586057›Full record

ArticleNeuron2026

Developmentally defined subcircuits in the hippocampus support spatial learning.

Roman Huszár, Artem Kirsanov, Griffin Henze, Dhananjay Huilgol, Manuel Valero, Z Josh Huang, György Buzsáki

Abstract read
In one paragraph

Article in Neuron, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Roman HuszárNeuroscience Institute, New York University Grossman School of Medicine, New York, NY 10016, USA; Center for Neural Science, New York University, New York, NY 10003, USA.
Artem KirsanovCenter for Neural Science, New York University, New York, NY 10003, USA.
Griffin HenzeCenter for Neural Science, New York University, New York, NY 10003, USA.
Dhananjay HuilgolDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
Manuel ValeroHospital del Mar Medical Research Institute, Barcelona, Spain.
Z Josh HuangDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
György BuzsákiNeuroscience Institute, New York University Grossman School of Medicine, New York, NY 10016, USA; Center for Neural Science, New York University, New York, NY 10003, USA. Electronic address: gyorgy.buzsaki@nyulangone.org.

Funding

U19 Supplement 2023-FroemkeU19NS107616 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MOSES VICTOR CHAO · 2018 to 2026
$36.4M
Transformation of Neuronal Activity in the Entorhinal-hippocampal-neocortex PathR01MH122391 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BASU, JAYEETA, BUZSAKI, GYORGY · 2020 to 2024
$3.3M
Consolidation and interference of hippocampal spatial mapsR01MH139216 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GYORGY BUZSAKI, KAMRAN DIBA · 2025 to 2026
$1.2M
NIMH NIH HHS R01 MH122391NIMH NIH HHS R01 MH139216NINDS NIH HHS U19 NS107616
6 · The paper itself

Abstract

Hippocampal circuits are composed of cells that exhibit heterogeneity in gene expression, connectivity, and intrinsic properties. This diversity arises during embryonic development, which produces parallel subcircuits along the trisynaptic pathway. To examine how these subcircuits support spatial memory, we combined embryonic birthdating of interconnected CA3-CA1 neurons with electrophysiology in a place-reward association task. Learning reorganized correlation patterns near rewarded locations, which were reactivated during sleep and predicted memory retrieval. Neurons born on the same day exhibited correlated activity across brain states and hippocampal subfields. Throughout learning, same-birthdate CA1 neurons coordinated their activity to encode the rewarded locations, but CA3 cells did not. These regional differences were mirrored by distinct patterns of connectivity between same-birthdate pyramidal cells and inhibitory interneurons. In particular, same-birthdate neurons converged onto parvalbumin-expressing CA1 interneurons, which were modulated by spatial learning. Together, our results demonstrate that development-defined subcircuits in the hippocampus are preconfigured to encode new memories.

Indexed as

birthdatingcodingdevelopmenthippocampusinterneuronslearningmemorynavigation

Identifiers

PMID42586057
PMCPMC13573635

What OpenQuestion holds

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Registered trials

None linked

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.