Evidence map›Paper›PMID 25632134›Full record

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

A distinct subtype of dopaminergic interneuron displays inverted structural plasticity at the axon initial segment.

Annisa N Chand, Elisa Galliano, Robert A Chesters, Matthew S Grubb

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 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
4.5field-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

65 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Primary cilia and neural computation.Journal of biomedical science · 2026
    Review
  3. Article
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  6. Article
  7. Article
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  10. Article
  11. Review
  12. Review
  13. The Primary Cilia are Associated with the Axon Initial Segment in Neurons.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  14. Article
  15. Article
  16. Intrinsic Plasticity Mechanisms of Repetitive Transcranial Magnetic Stimulation.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2024
    Review
  17. Article
  18. Article
  19. Review
  20. CDK5/p35-Dependent Microtubule Reorganization Contributes to Homeostatic Shortening of the Axon Initial Segment.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article

5 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

4 authors at 1 institution in 1 country.

Annisa N ChandMedical Research Council Centre for Developmental Neurobiology, King's College London, London SE1 1UL, United Kingdom.ORCID http://orcid.org/0000-0002-0178-1094
Elisa GallianoMedical Research Council Centre for Developmental Neurobiology, King's College London, London SE1 1UL, United Kingdom.ORCID http://orcid.org/0000-0002-6941-766X
Robert A ChestersMedical Research Council Centre for Developmental Neurobiology, King's College London, London SE1 1UL, United Kingdom.
Matthew S GrubbMedical Research Council Centre for Developmental Neurobiology, King's College London, London SE1 1UL, United Kingdom matthew.grubb@kcl.ac.uk.ORCID http://orcid.org/0000-0002-2673-274X
King's College London · GB

Funding

Medical Research Council G0901899Wellcome Trust
6 · The paper itself

Abstract

The axon initial segment (AIS) is a specialized structure near the start of the axon that is a site of neuronal plasticity. Changes in activity levels in vitro and in vivo can produce structural AIS changes in excitatory cells that have been linked to alterations in excitability, but these effects have never been described in inhibitory interneurons. In the mammalian olfactory bulb (OB), dopaminergic interneurons are particularly plastic, undergoing constitutive turnover throughout life and regulating tyrosine hydroxylase expression in an activity-dependent manner. Here we used dissociated cultures of rat and mouse OB to show that a subset of bulbar dopaminergic neurons possess an AIS and that these AIS-positive cells are morphologically and functionally distinct from their AIS-negative counterparts. Under baseline conditions, OB dopaminergic AISs were short and located distally along the axon but, in response to chronic 24 h depolarization, lengthened and relocated proximally toward the soma. These activity-dependent changes were in the opposite direction to both those we saw in non-GABAergic OB neurons and those reported previously for excitatory cell types. Inverted AIS plasticity in OB dopaminergic cells was bidirectional, involved all major components of the structure, was dependent on the activity of L-type CaV1 calcium channels but not on the activity of the calcium-activated phosphatase calcineurin, and was opposed by the actions of cyclin-dependent kinase 5. Such distinct forms of AIS plasticity in inhibitory interneurons and excitatory projection neurons may allow considerable flexibility when neuronal networks must adapt to perturbations in their ongoing activity.

Indexed as

AnimalsAnimals, NewbornAxonsCells, CulturedCyclin-Dependent Kinase 5Dopaminergic NeuronsEmbryo, MammalianFemaleLuminescent ProteinsMaleMiceMice, Inbred C57BLMice, TransgenicNeuronal PlasticityOlfactory BulbRatsCyclin-Dependent Kinase 5Luminescent ProteinsSodium Channel BlockersTetrodotoxinTyrosine 3-Monooxygenaseaxon initial segmentdopamineinterneuronolfactory bulbplasticity

Identifiers

PMID25632134
PMCPMC4308603
OpenAlexW2121389540

What OpenQuestion holds

Textmetadata
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.