Evidence map›Paper›PMID 39875374›Full record

ArticleNature communications2025

Sub-cellular population imaging tools reveal stable apical dendrites in hippocampal area CA3.

Jason J Moore, Shannon K Rashid, Emmett Bicker, Cara D Johnson, Naomi Codrington, Dmitri B Chklovskii, Jayeeta Basu

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Distinct types of dendritic CaScience advances · 2026
    Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jason J MooreNeuroscience Institute, New York University Langone Health, New York, NY, 10016, USA. Jason.Moore@nyulangone.org.ORCID http://orcid.org/0000-0002-4209-3896
Shannon K RashidNeuroscience Institute, New York University Langone Health, New York, NY, 10016, USA.
Emmett BickerNeuroscience Institute, New York University Langone Health, New York, NY, 10016, USA.ORCID http://orcid.org/0009-0004-0286-5654
Cara D JohnsonNeuroscience Institute, New York University Langone Health, New York, NY, 10016, USA.ORCID http://orcid.org/0000-0002-0264-6222
Naomi CodringtonNeuroscience Institute, New York University Langone Health, New York, NY, 10016, USA.
Dmitri B ChklovskiiNeuroscience Institute, New York University Langone Health, New York, NY, 10016, USA.
Jayeeta BasuNeuroscience Institute, New York University Langone Health, New York, NY, 10016, USA. Jayeeta.Basu@nyulangone.org.ORCID http://orcid.org/0000-0002-7559-0936

Funding

MEDICAL SCIENTIST TRAININGT32GM007308 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PHILIPS, MARK REID · 1985 to 2019
$23.2M
Reexamining the Role of Dendrites in Neuronal FunctionRM1NS132981 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Jayeeta Basu, RAFAEL YUSTE · 2023 to 2026
$10.3M
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
Postdoctoral Research Training in Neurodegenerative Disorders and the Aging BrainT32AG052909 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Helen E Scharfman, THOMAS M WISNIEWSKI · 2017 to 2026
$2.5M
Linking Plasticity of Hippocampal Representation across the Single Neuron and Circuit LevelsR01NS109994 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BASU, JAYEETA, CLOPATH, CLAUDIA · 2018 to 2022
$2.4M
Synaptic and Circuit Interactions to Shape Multisensory Processing - Administrative SupplementR01NS109362 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BASU, JAYEETA · 2018 to 2023
$1.9M
NIA NIH HHS T32 AG052909NIGMS NIH HHS T32 GM007308NIMH NIH HHS R01 MH122391NINDS NIH HHS R01 NS109362NINDS NIH HHS R01 NS109994NINDS NIH HHS RM1 NS132981U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) 5R01MH122391U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1R01NS109362-01U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1R01NS109994U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1RM1NS132981-01
6 · The paper itself

Abstract

Apical and basal dendrites of pyramidal neurons receive anatomically and functionally distinct inputs, implying compartment-level functional diversity during behavior. To test this, we imaged in vivo calcium signals from soma, apical dendrites, and basal dendrites in mouse hippocampal CA3 pyramidal neurons during head-fixed navigation. To capture compartment-specific population dynamics, we developed computational tools to automatically segment dendrites and extract accurate fluorescence traces from densely labeled neurons. We validated the method on sparsely labeled preparations and synthetic data, predicting an optimal labeling density for high experimental throughput and analytical accuracy. Our method detected rapid, local dendritic activity. Dendrites showed robust spatial tuning, similar to soma but with higher activity rates. Across days, apical dendrites remained more stable and outperformed in decoding of the animal's position. Thus, population-level apical and basal dendritic differences may reflect distinct compartment-specific input-output functions and computations in CA3. These tools will facilitate future studies mapping sub-cellular activity and their relation to behavior.

Indexed as

CA3 Region, HippocampalDendritesPyramidal CellsAnimalsCalciumMaleMiceMice, Inbred C57BLCalcium

Identifiers

PMID39875374
PMCPMC11775317

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.