Evidence map›Paper›PMID 21795548›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Cell-type-specific CCK2 receptor signaling underlies the cholecystokinin-mediated selective excitation of hippocampal parvalbumin-positive fast-spiking basket cells.

Soo Yeun Lee, Csaba Földy, János Szabadics, Ivan Soltesz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.3field-weighted citation impact, top 13% of its field
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

39 citing papers in PubMed, 64 citations in OpenAlex.

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  19. Cholecystokinin-Expressing Interneurons of the Medial Prefrontal Cortex Mediate Working Memory Retrieval.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
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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

4 authors at 3 institutions in 2 countries.

Soo Yeun LeeDepartment of Anatomy and Neurobiology, University of California, Irvine, Irvine, California 92697, USA. leesyn@uci.edu
Csaba Földy
János Szabadics
Ivan Soltesz
University of California, Irvine · USHungarian Academy of Sciences · HUStanford University · US

Funding

LIMBIC EXCITABILITY AFTER FEBRILE SEIZURESR01NS038580 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI SOLTESZ, IVAN · 1999 to 2010
$2.9M
NINDS NIH HHS NS38580NINDS NIH HHS R01 NS038580
6 · The paper itself

Abstract

Parvalbumin-positive (PV+) fast-spiking basket cells are thought to play key roles in network functions related to precise time keeping during behaviorally relevant hippocampal synchronous oscillations. Although they express relatively few receptors for neuromodulators, the highly abundant and functionally important neuropeptide cholecystokinin (CCK) is able to selectively depolarize PV+ basket cells, making these cells sensitive biosensors for CCK. However, the molecular mechanisms underlying the CCK-induced selective and powerful excitation of PV+ basket cells are not understood. We used single and paired patch-clamp recordings in acute rat hippocampal slices, in combination with post hoc identification of the recorded interneurons, to demonstrate that CCK acts via G-protein-coupled CCK2 receptors to engage sharply divergent intracellular pathways to exert its cell-type-selective effects. In contrast to CCK2 receptors on pyramidal cells that signal through the canonical G(q)-PLC pathway to trigger endocannabinoid-mediated signaling events, CCK2 receptors on neighboring PV+ basket cells couple to an unusual, pertussis-toxin-sensitive pathway. The latter pathway involves ryanodine receptors on intracellular calcium stores that ultimately activate a nonselective cationic conductance to depolarize PV+ basket cells. CCK has highly cell-type-selective effects even within the PV+ cell population, as the PV+ dendrite-targeting bistratified cells do not respond to CCK. Together, these results demonstrate that an abundant ligand such as CCK can signal through the same receptor in different neurons to use cell-type-selective signaling pathways to provide divergence and specificity to its effects.

Indexed as

Action PotentialsAnimalsAnimals, NewbornBenzodiazepinesCalciumChelating AgentsCholecystokininEgtazic AcidElectric StimulationEstrenesGuanosine DiphosphateHippocampusHormone AntagonistsIn Vitro TechniquesNeuronsParvalbumins1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dioneBenzodiazepinesCalciumChelating AgentsCholecystokininEgtazic AcidEstrenesguanosine 5'-O-(2-thiodiphosphate)Guanosine DiphosphateHormone AntagonistsParvalbuminsPhosphodiesterase InhibitorsPyrrolidinonesReceptor, Cholecystokinin BSodium Channel BlockersTetrodotoxinThionucleotidesYM 022

Identifiers

PMID21795548
PMCPMC3158608
OpenAlexW1974599985

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.