Evidence map›Paper›PMID 21602822›Full record

ArticleNature neuroscience2011

The SK2-long isoform directs synaptic localization and function of SK2-containing channels.

Duane Allen, Chris T Bond, Rafael Luján, Carmen Ballesteros-Merino, Mike T Lin, Kang Wang, Nathan Klett, Masahiko Watanabe, Ryuichi Shigemoto, Robert W Stackman and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

46 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The small conductance CaNeuropharmacology · 2024
    Article
  5. Article
  6. Article
  7. KJournal of neuroscience research · 2023
    Review
  8. KCurrent neuropharmacology · 2023
    Review
  9. Review
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  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Infection-induced endothelial amyloids impair memory.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  19. Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  20. Probing Single SynapsesFrontiers in synaptic neuroscience · 2019
    Article
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

12 authors at 6 institutions in 3 countries.

Duane AllenVollum Institute, Oregon Health & Science University, Portland, Oregon, USA.
Chris T Bond
Rafael Luján
Carmen Ballesteros-Merino
Mike T Lin
Kang Wang
Nathan Klett
Masahiko Watanabe
Ryuichi Shigemoto
Robert W Stackman
James Maylie
John P Adelman
Oregon Health & Science University · USVollum Institute · USUniversity of Castilla-La Mancha · ESFlorida Atlantic University · USHokkaido University · JPNational Institute for Physiological Sciences · JP

Funding

Molecular Physiology of the SK2 Channels in CA1 NeuronsR01NS038880 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI MAYLIE, JAMES G · 2000 to 2017
$6.0M
SK channels: Roles and mechanisms for dendritic excitability and plasticityR01MH081860 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI MAYLIE, JAMES G · 2008 to 2012
$1.6M
Memory modulation by SK channelsR01MH086591 · NIMH · FLORIDA ATLANTIC UNIVERSITY · PI STACKMAN, ROBERT WILLIAM · 2009 to 2013
$1.5M
SK2-associated protein kinase CK2: molecular basis and physiological rolesR01MH076752 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI ADELMAN, JOHN P · 2006 to 2010
$1.4M
Activity Dependent Modulation of SK2 ChannelsF32MH080480 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI LIN, MIKE T · 2008 to 2009
$105k
NIMH NIH HHS F32 MH080480NIMH NIH HHS F32MH080480NIMH NIH HHS MH081860-01NIMH NIH HHS MH0876591-01NIMH NIH HHS R01 MH076752NIMH NIH HHS R01 MH081860NIMH NIH HHS R01 MH086591NINDS NIH HHS NS038880NINDS NIH HHS R01 NS038880
6 · The paper itself

Abstract

SK2-containing channels are expressed in the postsynaptic density (PSD) of dendritic spines on mouse hippocampal area CA1 pyramidal neurons and influence synaptic responses, plasticity and learning. The Sk2 gene (also known as Kcnn2) encodes two isoforms that differ only in the length of their N-terminal domains. SK2-long (SK2-L) and SK2-short (SK2-S) are coexpressed in CA1 pyramidal neurons and likely form heteromeric channels. In mice lacking SK2-L (SK2-S only mice), SK2-S-containing channels were expressed in the extrasynaptic membrane, but were excluded from the PSD. The SK channel contribution to excitatory postsynaptic potentials was absent in SK2-S only mice and was restored by SK2-L re-expression. Blocking SK channels increased the amount of long-term potentiation induced in area CA1 in slices from wild-type mice but had no effect in slices from SK2-S only mice. Furthermore, SK2-S only mice outperformed wild-type mice in the novel object recognition task. These results indicate that SK2-L directs synaptic SK2-containing channel expression and is important for normal synaptic signaling, plasticity and learning.

Indexed as

AnimalsCA1 Region, HippocampalExcitatory Postsynaptic PotentialsLong-Term PotentiationMiceMice, KnockoutPost-Synaptic DensityProtein IsoformsPyramidal CellsSignal TransductionSmall-Conductance Calcium-Activated Potassium ChannelsSynapsesKcnn2 protein, mouseProtein IsoformsSmall-Conductance Calcium-Activated Potassium Channels

Identifiers

PMID21602822
PMCPMC3417338
OpenAlexW2068872819

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.