Evidence map›Paper›PMID 25798106›Full record

ArticleFrontiers in synaptic neuroscience2015

Hippocampal "cholinergic interneurons" visualized with the choline acetyltransferase promoter: anatomical distribution, intrinsic membrane properties, neurochemical characteristics, and capacity for cholinergic modulation.

Feng Yi, Elizabeth Catudio-Garrett, Robert Gábriel, Marta Wilhelm, Ferenc Erdelyi, Gabor Szabo, Karl Deisseroth, Josh Lawrence

Abstract read
In one paragraph

Article in Frontiers in synaptic neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

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  10. Deficits in Behavioral and Neuronal Pattern Separation in Temporal Lobe Epilepsy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
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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

8 authors.

Feng YiCOBRE Center for Structural and Functional Neuroscience, The University of Montana Missoula, MT, USA ; Department of Biomedical and Pharmaceutical Sciences, The University of Montana Missoula, MT, USA.
Elizabeth Catudio-GarrettCOBRE Center for Structural and Functional Neuroscience, The University of Montana Missoula, MT, USA ; Department of Biomedical and Pharmaceutical Sciences, The University of Montana Missoula, MT, USA ; Davidson's Honors College, The University of Montana Missoula, MT, USA.
Robert GábrielDepartment of Experimental Zoology and Neurobiology, University of Pécs Pécs, Hungary ; János Szentágothai Research Center Pécs, Hungary.
Marta WilhelmDepartment of Experimental Zoology and Neurobiology, University of Pécs Pécs, Hungary ; Department of Sport Biology, University of Pécs Pécs, Hungary.
Ferenc ErdelyiLaboratory of Molecular Biology and Genetics, Institute of Experimental Medicine, Hungarian Academy of Sciences Budapest, Hungary.
Gabor SzaboLaboratory of Molecular Biology and Genetics, Institute of Experimental Medicine, Hungarian Academy of Sciences Budapest, Hungary.
Karl DeisserothDepartment of Bioengineering, Stanford University Stanford, CA, USA.
Josh LawrenceCOBRE Center for Structural and Functional Neuroscience, The University of Montana Missoula, MT, USA ; Department of Biomedical and Pharmaceutical Sciences, The University of Montana Missoula, MT, USA.

Funding

THE ROLE OF PULMONARY SUBPOPULATIONS AND TH2 IMMUNITY IN BALB/C SILICOSIS MODELP20RR017670 · NCRR · UNIVERSITY OF MONTANA · PI ROBERTS, KEVAN · 2002 to 2011
$22.0M
Understanding the molecular mechanism of pathogenesis of prion diseasesP20RR015583 · NCRR · UNIVERSITY OF MONTANA · PI KAVANAUGH, MICHAEL PATRICK · 2000 to 2009
$17.6M
Differential modes of cholinergic transmission onto cellular hippocampal targetsR01NS069689 · NINDS · UNIVERSITY OF MONTANA · PI LAWRENCE, JOHN JOSHUA · 2010 to 2014
$1.5M
NCRR NIH HHS P20 RR015583NCRR NIH HHS P20 RR017670NINDS NIH HHS R01 NS069689
6 · The paper itself

Abstract

Release of acetylcholine (ACh) in the hippocampus (HC) occurs during exploration, arousal, and learning. Although the medial septum-diagonal band of Broca (MS-DBB) is the major extrinsic source of cholinergic input to the HC, cholinergic neurons intrinsic to the HC also exist but remain poorly understood. Here, ChAT-tauGFP and ChAT-CRE/Rosa26YFP (ChAT-Rosa) mice were examined in HC. The HC of ChAT-tauGFP mice was densely innervated with GFP-positive axons, often accompanied by large GFP-positive structures, some of which were Neurotrace/DAPI-negative and likely represent large axon terminals. In the HC of ChAT-Rosa mice, ChAT-YFP cells were Neurotrace-positive and more abundant in CA3 and dentate gyrus than CA1 with partial overlap with calretinin/VIP. Moreover, an anti-ChAT antibody consistently showed ChAT immunoreactivity in ChAT-YFP cells from MS-DBB but rarely from HC. Furthermore, ChAT-YFP cells from CA1 stratum radiatum/stratum lacunosum moleculare (SR/SLM) exhibited a stuttering firing phenotype but a delayed firing phenotype in stratum pyramidale (SP) of CA3. Input resistance and capacitance were also different between CA1 SR/LM and CA3 SP ChAT-YFP cells. Bath application of ACh increased firing frequency in all ChAT-YFP cells; however, cholinergic modulation was larger in CA1 SR/SLM than CA3 SP ChAT-YFP cells. Finally, CA3 SP ChAT-YFP cells exhibited a wider AP half-width and weaker cholinergic modulation than YFP-negative CA3 pyramidal cells. Consistent with CRE expression in a subpopulation of principal cells, optogenetic stimulation evoked glutamatergic postsynaptic currents in CA1 SR/SLM interneurons. In conclusion, the presence of fluorescently labeled hippocampal cells common to both ChAT-tauGFP and ChAT-Rosa mice are in good agreement with previous reports on the existence of cholinergic interneurons, but both transgenic mouse lines exhibited unexpected anatomical features that departed considerably from earlier observations.

Indexed as

cholinergic modulationglutamate transmissionhippocampusoptogeneticstransgenic mice

Identifiers

PMID25798106
PMCPMC4351620

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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.