Evidence map›Paper›PMID 26538660›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Distinct Cell- and Layer-Specific Expression Patterns and Independent Regulation of Kv2 Channel Subtypes in Cortical Pyramidal Neurons.

Hannah I Bishop, Dongxu Guan, Elke Bocksteins, Laxmi Kumar Parajuli, Karl D Murray, Melanie M Cobb, Hiroaki Misonou, Karen Zito, Robert C Foehring, James S Trimmer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 2 pooled it
4.2field-weighted citation impact, top 5% 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

70 citing papers in PubMed, 2 syntheses or guidelines pooled it, 106 citations in OpenAlex.

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  11. The Electrically Silent Kv5.1 Subunit Forms Heteromeric Kv2 Channels in Cortical Neurons and Confers Distinct Functional Properties.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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10 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

10 authors at 5 institutions in 4 countries.

Hannah I BishopDepartment of Neurobiology, Physiology and Behavior and.ORCID http://orcid.org/0000-0002-5846-5885
Dongxu GuanDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee 38163.
Elke BocksteinsDepartment of Biomedical Sciences, Laboratory for Molecular Biophysics, Physiology, and Pharmacology, University of Antwerp, 2610 Antwerp, Belgium.
Laxmi Kumar ParajuliCenter for Neuroscience, University of California, Davis, California 95616.
Karl D MurrayCenter for Neuroscience, University of California, Davis, California 95616.
Melanie M CobbDepartment of Neurobiology, Physiology and Behavior and.
Hiroaki MisonouGraduate School of Brain Science, Doshisha University, Kyoto 619-0225, Japan, and.ORCID http://orcid.org/0000-0001-5892-1804
Karen ZitoDepartment of Neurobiology, Physiology and Behavior and Center for Neuroscience, University of California, Davis, California 95616.
Robert C FoehringDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, Tennessee 38163.
James S TrimmerDepartment of Neurobiology, Physiology and Behavior and Department of Physiology and Membrane Biology, University of California Davis School of Medicine, Davis, California 95616 jtrimmer@ucdavis.edu.ORCID http://orcid.org/0000-0002-6117-3912
Institute of Neurobiology · BGUniversity of California, Davis · USUniversity of Tennessee Health Science Center · USDoshisha University · JPUniversity of Antwerp · BE

Funding

Slowly Inactivating K+ Channels in Pyramidal NeuronsR01NS044163 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI FOEHRING, ROBERT C, SPAIN, WILLIAM J · 2003 to 2022
$6.5M
Determinants of Dendritic Potassium Channel LocalizationR01NS042225 · NINDS · UNIVERSITY OF CALIFORNIA DAVIS · PI TRIMMER, JAMES S · 2001 to 2014
$6.3M
Mechanisms of Dendritic Spine EliminationR01NS062736 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ZITO, KAREN · 2009 to 2019
$3.8M
NINDS NIH HHS R01 NS042225NINDS NIH HHS R01 NS044163NINDS NIH HHS R01 NS062736
6 · The paper itself

Abstract

The Kv2 family of voltage-gated potassium channel α subunits, comprising Kv2.1 and Kv2.2, mediate the bulk of the neuronal delayed rectifier K(+) current in many mammalian central neurons. Kv2.1 exhibits robust expression across many neuron types and is unique in its conditional role in modulating intrinsic excitability through changes in its phosphorylation state, which affect Kv2.1 expression, localization, and function. Much less is known of the highly related Kv2.2 subunit, especially in forebrain neurons. Here, through combined use of cortical layer markers and transgenic mouse lines, we show that Kv2.1 and Kv2.2 are localized to functionally distinct cortical cell types. Kv2.1 expression is consistently high throughout all cortical layers, especially in layer (L) 5b pyramidal neurons, whereas Kv2.2 expression is primarily limited to neurons in L2 and L5a. In addition, L4 of primary somatosensory cortex is strikingly devoid of Kv2.2 immunolabeling. The restricted pattern of Kv2.2 expression persists in Kv2.1-KO mice, suggesting distinct cell- and layer-specific functions for these two highly related Kv2 subunits. Analyses of endogenous Kv2.2 in cortical neurons in situ and recombinant Kv2.2 expressed in heterologous cells reveal that Kv2.2 is largely refractory to stimuli that trigger robust, phosphorylation-dependent changes in Kv2.1 clustering and function. Immunocytochemistry and voltage-clamp recordings from outside-out macropatches reveal distinct cellular expression patterns for Kv2.1 and Kv2.2 in intratelencephalic and pyramidal tract neurons of L5, indicating circuit-specific requirements for these Kv2 paralogs. Together, these results support distinct roles for these two Kv2 channel family members in mammalian cortex. SIGNIFICANCE STATEMENT: Neurons within the neocortex are arranged in a laminar architecture and contribute to the input, processing, and/or output of sensory and motor signals in a cell- and layer-specific manner. Neurons of different cortical layers express diverse populations of ion channels and possess distinct intrinsic membrane properties. Here, we show that the Kv2 family members Kv2.1 and Kv2.2 are expressed in distinct cortical layers and pyramidal cell types associated with specific corticostriatal pathways. We find that Kv2.1 and Kv2.2 exhibit distinct responses to acute phosphorylation-dependent regulation in brain neurons in situ and in heterologous cells in vitro. These results identify a molecular mechanism that contributes to heterogeneity in cortical neuron ion channel function and regulation.

Indexed as

AnimalsCells, CulturedGene Expression RegulationHEK293 CellsHumansMiceMice, Inbred C57BLMice, KnockoutNeocortexNeuronsOrgan Culture TechniquesPyramidal CellsRatsRats, Sprague-DawleyShab Potassium ChannelsShab Potassium Channelselectrophysiologyimmunohistochemistrylocalizationmodulationneocortexnetwork

Identifiers

PMID26538660
PMCPMC4635138
OpenAlexW2340166006

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.