Evidence map›Paper›PMID 27346528›Full record

ArticleNeuron2016

Synapse-Level Determination of Action Potential Duration by K(+) Channel Clustering in Axons.

Matthew J M Rowan, Gina DelCanto, Jianqing J Yu, Naomi Kamasawa, Jason M Christie

Abstract read
In one paragraph

Article in Neuron, 2016. 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
–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

46 citing papers in PubMed.

  1. Article
  2. Article
  3. Molecular mechanism governing the plasticity of use-dependent spike broadening in dorsal root ganglion neurons.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Beyond a Transmission Cable-New Technologies to Reveal the Richness in Axonal Electrophysiology.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  6. Article
  7. Article
  8. Regulation of Neurotransmitter Release by KAdvances in neurobiology · 2023
    Article
  9. The computational power of the human brain.Frontiers in cellular neuroscience · 2023
    Review
  10. Biophysical KeLife · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Sparsely Distributed, Pre-synaptic Kv3 KFrontiers in cellular neuroscience · 2021
    Article
  18. Article
  19. Article
  20. Adult-Born Hippocampal Neurons Undergo Extended Development and Are Morphologically Distinct from Neonatally-Born Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    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

5 authors.

Matthew J M RowanMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
Gina DelCantoWilkes Honors Campus of Florida Atlantic University, Jupiter, FL 33405, USA.
Jianqing J YuMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
Naomi KamasawaMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA.
Jason M ChristieMax Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA. Electronic address: jason.christie@mpfi.org.

Funding

Action Potential Signaling in Axons of CNS InterneuronsR01NS083894 · NINDS · MAX PLANCK FLORIDA CORPORATION · PI CHRISTIE, JASON M · 2013 to 2017
$2.1M
Local control of the action potential in axonsF32NS083127 · NINDS · MAX PLANCK FLORIDA CORPORATION · PI ROWAN, MATTHEW J.M. · 2014 to 2016
$169k
NINDS NIH HHS F32 NS083127NINDS NIH HHS R01 NS083894
6 · The paper itself

Abstract

In axons, an action potential (AP) is thought to be broadcast as an unwavering binary pulse over its arbor, driving neurotransmission uniformly at release sites. Yet by recording from axons of cerebellar stellate cell (SC) interneurons, we show that AP width varies between presynaptic bouton sites, even within the same axon branch. The varicose geometry of SC boutons alone does not impose differences in spike duration. Rather, axonal patching revealed heterogeneous peak conductance densities of currents mediated mainly by fast-activating Kv3-type potassium channels, with clustered hotspots at boutons and restricted expression at adjoining shafts. Blockade of Kv channels at individual boutons indicates that currents immediately local to a release site direct spike repolarization at that location. Thus, the clustered arrangement and variable expression density of Kv3 channels at boutons are key determinants underlying compartmentalized control of AP width in a near synapse-by-synapse manner, multiplying the signaling capacity of these structures.

Indexed as

Action PotentialsAnimalsAxonsCerebellumInterneuronsMice, Inbred C57BLPatch-Clamp TechniquesPotassium ChannelsPresynaptic TerminalsSynapsesSynaptic TransmissionPotassium Channels

Identifiers

PMID27346528
PMCPMC4969170

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.