Evidence map›Paper›PMID 23897576›Full record

ArticleThe Journal of comparative neurology2014

Subcellular localization of intercellular adhesion molecule-5 (telencephalin) in the visual cortex is not developmentally regulated in the absence of matrix metalloproteinase-9.

Emily A Kelly, Marie-Eve Tremblay, Carl G Gahmberg, Li Tian, Ania K Majewska

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  5. Review
  6. Review
  7. Article
  8. MMPs in learning and memory and neuropsychiatric disorders.Cellular and molecular life sciences : CMLS · 2019
    Review
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  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
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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 at 2 institutions in 2 countries.

Emily A KellyDepartment of Neurobiology and Anatomy, University of Rochester, Rochester, New York, 14642.
Marie-Eve Tremblay
Carl G Gahmberg
Li Tian
Ania K Majewska
University of Rochester · USUniversity of Helsinki · FI

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI Martha Susiarjo · 1985 to 2026
$42.8M
Training in Environment ToxicologyT32ES007026 · NIEHS · UNIVERSITY OF ROCHESTER · PI Alison Elder, Marissa Sobolewski Terry · 1985 to 2026
$20.2M
Imaging visual plasticity in vivo.R01EY019277 · NEI · UNIVERSITY OF ROCHESTER · PI MAJEWSKA, ANNA K · 2009 to 2016
$2.6M
VISUAL COMPUTATIONS FOR MOTOR CONTROLR01EY013319 · NEI · UNIVERSITY OF ROCHESTER · PI KNILL, DAVID C · 2001 to 2009
$2.6M
CIHRNEI NIH HHS EY013319NEI NIH HHS EY019277NEI NIH HHS R01 EY013319NEI NIH HHS R01 EY019277NIEHS NIH HHS P30 ES001247NIEHS NIH HHS T32 ES007026NIEHS NIH HHS T32 ES 7026-34
6 · The paper itself

Abstract

The telencephalon-associated intercellular adhesion molecule-5 (telencephalin; ICAM-5) regulates dendritic morphology in the developing brain. In vitro studies have shown that ICAM-5 is found predominantly within dendrites and immature dendritic protrusions, with reduced expression in mushroom spines, suggesting that ICAM-5 downregulation is critical for the maturation of synaptic structures. However, developmental expression of ICAM-5 has not been explored in depth at the ultrastructural level in intact brain tissue. To investigate the ultrastructural localization of ICAM-5 with transmission electron microscopy, we performed immunoperoxidase histochemistry for ICAM-5 in mouse visual cortex at postnatal day (P)14, a period of intense synaptogenesis, and at P28, when synapses mature. We observed the expected ICAM-5 expression in dendritic protrusions and shafts at both P14 and P28. ICAM-5 expression in these dendritic protrusions decreased in prevalence with developmental age to become localized predominantly to dendritic shafts by P28. To understand better the relationship between ICAM-5 and the endopeptidase metalloproteinase-9 (MMP-9), which mediates ICAM-5 cleavage following glutamate activation during postnatal development, we also explored ICAM-5 expression in MMP-9 null animals. This analysis revealed a similar expression of ICAM-5 in dendritic elements at P14 and P28; however, an increased prevalence of ICAM-5 was noted in dendritic protrusions at P28 in the MMP-9 null animals, indicating that, in the absence of MMP-9, there is no developmental shift in ICAM-5 subcellular localization. Our ultrastructural observations shed light on possible functions mediated by ICAM-5 and their regulation by extracellular proteases.

Indexed as

AnimalsAnimals, NewbornAxonsCalcium-Binding ProteinsDendritesGene Expression Regulation, DevelopmentalGlial Fibrillary Acidic ProteinMatrix Metalloproteinase 9Membrane GlycoproteinsMiceMice, KnockoutMicrofilament ProteinsMicroscopy, ImmunoelectronNerve Tissue ProteinsNeuronsPhosphopyruvate HydrataseAif1 protein, mouseCalcium-Binding ProteinsGlial Fibrillary Acidic ProteinIcam5 protein, mouseMatrix Metalloproteinase 9Membrane GlycoproteinsMicrofilament ProteinsNerve Tissue ProteinsPhosphopyruvate Hydratasedendriteelectron microscopyICAM-5MMP-9plasticitytelencephalin

Identifiers

PMID23897576
PMCPMC3877171
OpenAlexW1527098129

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.