Evidence map›Paper›PMID 39665517›Full record

ArticleHippocampus2025

Field EPSPs of Dentate Gyrus Granule Cells Studied by Selective Optogenetic Activation of Hilar Mossy Cells in Hippocampal Slices.

Hannah L Bernstein, Yi-Ling Lu, Justin J Botterill, Áine M Duffy, John J LaFrancois, Helen E Scharfman

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Hannah L BernsteinDepartments of Child & Adolescent Psychiatry, Neuroscience & Physiology, and Psychiatry, and the Neuroscience Institute, New York University Langone Health, New York, New York, USA.
Yi-Ling LuDepartments of Child & Adolescent Psychiatry, Neuroscience & Physiology, and Psychiatry, and the Neuroscience Institute, New York University Langone Health, New York, New York, USA.
Justin J BotterillDepartments of Child & Adolescent Psychiatry, Neuroscience & Physiology, and Psychiatry, and the Neuroscience Institute, New York University Langone Health, New York, New York, USA.
Áine M DuffyDepartments of Child & Adolescent Psychiatry, Neuroscience & Physiology, and Psychiatry, and the Neuroscience Institute, New York University Langone Health, New York, New York, USA.
John J LaFrancoisDepartments of Child & Adolescent Psychiatry, Neuroscience & Physiology, and Psychiatry, and the Neuroscience Institute, New York University Langone Health, New York, New York, USA.
Helen E ScharfmanDepartments of Child & Adolescent Psychiatry, Neuroscience & Physiology, and Psychiatry, and the Neuroscience Institute, New York University Langone Health, New York, New York, USA.ORCID 0000-0003-4006-3383

Funding

Hilar mossy cells and dentate gyrus functionR01MH109305 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI SCHARFMAN, HELEN E · 2016 to 2020
$2.0M
Mossy Cells in Temporal Lobe EpilepsyR37NS126529 · NINDS · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI Helen E Scharfman · 2023 to 2026
$1.9M
Probing the function of hilar mossy cells in hippocampal circuits and dentate gyrus-dependent behaviorsF30MH110165 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BERNSTEIN, HANNAH LAURA · 2016 to 2018
$104k
Natural Sciences and Engineering Research Council of CanadaNew York State Office of Mental HealthNIH HHSNIMH NIH HHS F30 MH110165NIMH NIH HHS R01 MH109305NINDS NIH HHS R37 NS126529Savoy Foundation
6 · The paper itself

Abstract

Glutamatergic dentate gyrus (DG) mossy cells (MCs) innervate the primary DG cell type, granule cells (GCs). Numerous MC synapses are on GC proximal dendrites in the inner molecular layer (IML). However, field recordings of the GC excitatory postsynaptic potential (fEPSPs) have not been used to study this pathway selectively. Here we describe methods to selectively activate MC axons in the IML using mice with Cre recombinase expressed in MCs. Slices were made after injecting adeno-associated virus (AAV) encoding channelrhodopsin (ChR2) in the DG. In these slices, we show that fEPSPs could be recorded reliably in the IML in response to optogenetic stimulation of MC axons. Furthermore, fEPSPs were widespread across the septotemporal axis. However, fEPSPs were relatively weak because they were small in amplitude and did not elicit a significant population spike in GCs. They also showed little paired pulse facilitation. We confirmed the extracellular findings with patch clamp recordings of GCs despite different recording chambers and other differences in methods. Together the results provide a simple method for studying MC activation of GCs and add to the evidence that this input is normally weak but widespread across the GC population.

Indexed as

Dentate GyrusExcitatory Postsynaptic PotentialsMice, TransgenicMossy Fibers, HippocampalOptogeneticsAnimalsChannelrhodopsinsDependovirusIntegrasesIn Vitro TechniquesMaleMiceMice, Inbred C57BLNeuronsPatch-Clamp TechniquesChannelrhodopsinsCre recombinaseIntegrases

Identifiers

PMID39665517
PMCPMC11658804

What OpenQuestion holds

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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.