Evidence map›Paper›PMID 22607004›Full record

ArticleThe European journal of neuroscience2012

Termination and initial branch formation of SNAP-25-deficient thalamocortical fibres in heterochronic organotypic co-cultures.

Daniel Blakey, Michael C Wilson, Zoltán Molnár

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2012. 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. Development and Evolution of Thalamocortical Connectivity.Cold Spring Harbor perspectives in biology · 2024
    Review
  3. The role of snare proteins in cortical development.Developmental neurobiology · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Membrane Trafficking in Neuronal Development: Ins and Outs of Neural Connectivity.International review of cell and molecular biology · 2016
    Article
  9. Netrin-4 regulates thalamocortical axon branching in an activity-dependent fashion.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  10. Article
  11. Review
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

3 authors.

Daniel BlakeyDepartment of Physiology, Anatomy and Genetics, Le Gros Clark Building, University of Oxford, South Parks Road, Oxford OX1 3QX, UK.
Michael C Wilson
Zoltán Molnár

Funding

SNAP-25 EXPRESSION AND HYPERACTIVITY IN COLOBOMA MICER01MH048989 · NIMH · UNIVERSITY OF NEW MEXICO · PI WILSON, MICHAEL COLIN · 1992 to 2008
$2.7M
Gene X Environment Interactions in Synaptic Plasticity of Neural SystemsR21MH091464 · NIMH · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI WILSON, MICHAEL COLIN · 2010 to 2011
$404k
Medical Research Council G0900901NIMH NIH HHS R01 MH048989NIMH NIH HHS R01 MH48989NIMH NIH HHS R21 MH091464Wellcome Trust
6 · The paper itself

Abstract

We are interested in the role of neural activity mediated through regulated vesicular release in the stopping and early branching of the thalamic projections in the cortex. Axon outgrowth, arrival at the cortical subplate, side-branch formation during the waiting period and cortical plate innervation of embryonic thalamocortical projections occurs without major abnormalities in the absence of regulated release in Snap25 (-/-) null mutant mice [Washbourne et al. (2002) Nat. Neurosci. 5:19-26; Molnár et al. (2002) J. Neurosci. 22:10313-10323]. The fact that Snap25 (-/-) null mutant mice die at birth limited our previous experiments to the prenatal period. We therefore investigated the behaviour of thalamic projections in co-culture paradigms by using heterochronic thalamic [embryonic day (E)16-E18] and cortical [postnatal day (P)0-P3] explants, in which the stopping and branching behaviour has been previously documented. Our current co-culture experiments established that thalamic projections from E16-E18 Snap25(+/+) or Snap25 (-/-) explants behaved in an identical fashion in P0-P3 Snap25 (+/+) cortical explants after 7 days in vitro. Thalamic projections from Snap25 (-/-) explants developed similar patterns of fibre ingrowth to the cortex, and stopped and formed branches at a similar depth in the Snap25(+/+) cortical slice as in control cultures. These results imply that thalamic projections can reach their ultimate target cells in layer 4, stop, and start to develop branches in the absence of regulated vesicular transmitter release from their own terminals.

Indexed as

Cerebral CortexNeural PathwaysThalamusAmino AcidsAnimalsAnimals, NewbornAxonsCoculture TechniquesEmbryo, MammalianMiceMice, Inbred C57BLMice, KnockoutNeuronsOrgan Culture TechniquesStatistics, NonparametricSynaptosomal-Associated Protein 25Amino AcidsdolaisoleucineSnap25 protein, mouseSynaptosomal-Associated Protein 25

Identifiers

PMID22607004
PMCPMC3359864

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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.