Evidence map›Paper›PMID 21917805›Full record

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

Subunit-dependent axonal trafficking of distinct alpha heteromeric potassium channel complexes.

Paul M Jenkins, Jeremy C McIntyre, Lian Zhang, Arun Anantharam, Eileen D Vesely, Kristin L Arendt, Cynthia J L Carruthers, Tom K Kerppola, Jorge A Iñiguez-Lluhí, Ronald W Holz and 2 more

Abstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. IA channels: diverse regulatory mechanisms.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2014
    Review
  9. Article
  10. Article
  11. 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.

Paul M JenkinsDepartment of Pharmacology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Jeremy C McIntyre
Lian Zhang
Arun Anantharam
Eileen D Vesely
Kristin L Arendt
Cynthia J L Carruthers
Tom K Kerppola
Jorge A Iñiguez-Lluhí
Ronald W Holz
Michael A Sutton
Jeffrey R Martens

Funding

Sensory Mechanisms and Disorders - Administrative SupplementT32DC000011 · NIDCD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Michael Thomas Roberts · 1989 to 2026
$9.5M
Trafficking and Regulation of Cardiovascular K+ ChannelsR01HL070973 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MARTENS, JEFFREY · 2003 to 2013
$3.0M
Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging FR01GM086213 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KERPPOLA, TOM KLAUS, REDDY, KAREN LYNN · 2008 to 2011
$2.8M
Local Homeostatic Control of Synapse FunctionR01MH085798 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SUTTON, MICHAEL MARK ALEXANDER · 2010 to 2014
$1.9M
Structure/Function of Steroid Receptor AF1 CoregulatorsR01DK061656 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI INIGUEZ LLUHI, JORGE A · 2002 to 2006
$1.2M
Regulation of nuclear receptor function through SUMO ModificationR56DK061656 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI INIGUEZ LLUHI, JORGE A · 2008 to 2008
$77k
Howard Hughes Medical InstituteNHLBI NIH HHS R01 HL070973NIDCD NIH HHS T32 DC000011NIDDK NIH HHS DK61656-01NIDDK NIH HHS R01 DK061656NIDDK NIH HHS R56 DK061656NIGMS NIH HHS R01 GM086213NIMH NIH HHS R01 MH085798
6 · The paper itself

Abstract

Voltage-gated potassium (Kv) channels are critical for neuronal excitability and are targeted to specific subcellular compartments to carry out their unique functions. While it is widely believed that Kv channels exist as heteromeric complexes in neurons, direct tests of the hypothesis that specific heteromeric channel populations display divergent spatial and temporal dynamics are limited. Using a bimolecular fluorescence complementation approach, we monitored the assembly and localization of cell surface channel complexes in living cells. While PSD95-mediated clustering was subunit independent, selective visualization of heteromeric Kv complexes in rat hippocampal neurons revealed subunit-dependent localization that was not predicted by analyzing individual subunits. Assembly of Kv1.1 with Kv1.4 prevented axonal localization but not surface expression, while inclusion of Kv1.2 imparted clustering at presynaptic sites and decreased channel mobility within the axon. This mechanism by which specific Kv channel subunits can act in a dominant manner to impose unique trafficking properties to heteromeric complexes extended to Shab-related family of Kv channels. When coexpressed, Kv2.1 and Kv2.2 heteromultimers did not aggregate in somatodendritic clusters observed with expression of Kv2.1 alone. These studies demonstrate selective axonal trafficking and surface localization of distinct Kv channels based on their subunit composition.

Indexed as

AnimalsAxonal TransportCell MembraneCells, CulturedChlorocebus aethiopsCOS CellsFemaleHippocampusMaleMembrane PotentialsNeuronsPatch-Clamp TechniquesProtein SubunitsProtein TransportRatsShaker Superfamily of Potassium ChannelsProtein SubunitsShaker Superfamily of Potassium Channels

Identifiers

PMID21917805
PMCPMC3415696

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.