Evidence map›Paper›PMID 24097043›Full record

ArticleNature neuroscience2013

Dual origins of functionally distinct O-LM interneurons revealed by differential 5-HT(3A)R expression.

Ramesh Chittajallu, Michael T Craig, Ashley McFarland, Xiaoqing Yuan, Scott Gerfen, Ludovic Tricoire, Brian Erkkila, Sean C Barron, Carla M Lopez, Barry J Liang and 3 more

Abstract read
In one paragraph

Article in Nature neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing 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

75 citing papers in PubMed.

  1. Dendrite-Targeting Inhibitory Interneurons Form Biased Circuits with Deep and Superficial Pyramidal Cells in Hippocampal CA1.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
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  6. Functional specialization of hippocampal somatostatin-expressing interneurons.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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15 more citing papers are in PubMed but not listed here.

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

13 authors.

Ramesh Chittajallu1] Program in Developmental Neurobiology, Eunice Kennedy-Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health, Bethesda, Maryland, USA. [2].
Michael T Craig
Ashley McFarland
Xiaoqing Yuan
Scott Gerfen
Ludovic Tricoire
Brian Erkkila
Sean C Barron
Carla M Lopez
Barry J Liang
Brian W Jeffries
Kenneth A Pelkey
Chris J McBain

Funding

Cellular And Synaptic Physiology Of Hippocampal InterneuronsZIAHD001205 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI MCBAIN, CHRIS J. · 2009 to 2025
$45.8M
Intramural NIH HHS ZIA HD001205
6 · The paper itself

Abstract

Forebrain circuits rely upon a relatively small but remarkably diverse population of GABAergic interneurons to bind and entrain large principal cell assemblies for network synchronization and rhythmogenesis. Despite the high degree of heterogeneity across cortical interneurons, members of a given subtype typically exhibit homogeneous developmental origins, neuromodulatory response profiles, morphological characteristics, neurochemical signatures and electrical features. Here we report a surprising divergence among hippocampal oriens-lacunosum moleculare (O-LM) projecting interneurons that have hitherto been considered a homogeneous cell population. Combined immunocytochemical, anatomical and electrophysiological interrogation of Htr3a-GFP and Nkx2-1-cre:RCE mice revealed that O-LM cells parse into a caudal ganglionic eminence-derived subpopulation expressing 5-HT(3A) receptors (5-HT(3A)Rs) and a medial ganglionic eminence-derived subpopulation lacking 5-HT(3A)Rs. These two cohorts differentially participate in network oscillations, with 5-HT(3A)R-containing O-LM cell recruitment dictated by serotonergic tone. Thus, members of a seemingly uniform interneuron population can exhibit unique circuit functions and neuromodulatory properties dictated by disparate developmental origins.

Indexed as

Action PotentialsAge FactorsAnimalsAnimals, NewbornBasic Helix-Loop-Helix ProteinsCell MovementCholecystokininEmbryo, MammalianFemaleGene Expression Regulation, DevelopmentalHippocampusInterneuronsIn Vitro TechniquesLuminescent ProteinsLysineMaleAscl1 protein, mouseBasic Helix-Loop-Helix ProteinsbiocytinCholecystokininLuminescent ProteinsLysineNeurotransmitter AgentsNkx2-1 protein, mouseNuclear ProteinsReceptors, Serotonin, 5-HT3SomatostatinThyroid Nuclear Factor 1Transcription FactorsVasoactive Intestinal Peptide

Identifiers

PMID24097043
PMCPMC3839306

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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.