Evidence map›Paper›PMID 9712659›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1998

N-cadherin redistribution during synaptogenesis in hippocampal neurons.

D L Benson, H Tanaka

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

124 citing papers in PubMed, 307 citations in OpenAlex.

  1. Review
  2. Article
  3. Cadherin-13 Maintains Retinotectal Synapses via Transneuronal Interactions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  4. Article
  5. Article
  6. Delta-Catenin as a Modulator of Rho GTPases in Neurons.Frontiers in cellular neuroscience · 2022
    Review
  7. Molecular mechanisms of synaptogenesis.Frontiers in synaptic neuroscience · 2022
    Review
  8. Review
  9. Urokinase-type plasminogen activator promotes N-cadherin-mediated synaptic recovery in the ischemic brain.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  10. Review
  11. Article
  12. Urokinase-Type Plasminogen Activator Protects Cerebral Cortical Neurons from Soluble Aβ-Induced Synaptic Damage.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  13. Functions of p38 MAP Kinases in the Central Nervous System.Frontiers in molecular neuroscience · 2020
    Review
  14. Review
  15. Article
  16. Article
  17. The Cadherin Superfamily in Neural Circuit Assembly.Cold Spring Harbor perspectives in biology · 2018
    Review
  18. Article
  19. PKD1 Promotes Functional Synapse Formation Coordinated with N-Cadherin in Hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  20. Article

64 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

2 authors at 1 institution in 1 country.

D L BensonFishberg Research Center for Neurobiology, Mount Sinai School of Medicine, New York, New York 10029, USA.
H Tanaka
Icahn School of Medicine at Mount Sinai · US

Funding

ROLE OF INTEGRINS IN MYELINATIONP01NS033165 · NINDS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI LAZZARINI, ROBERT A · 1995 to 1999
–
ESTRADIOL MEDIATED DENDRITIC SPINE INDUCTIONR03AG015204 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BENSON, DEANNA L · 1997 to 1997
–
NIA NIH HHS AG15204-01NINDS NIH HHS 5 P01 NS33165
6 · The paper itself

Abstract

Cadherins are homophilic adhesion molecules that, together with their intracellular binding partners the catenins, mediate adhesion and signaling at a variety of intercellular junctions. This study shows that neural (N)-cadherin and beta-catenin, an intracellular binding partner for the classic cadherins, are present in axons and dendrites before synapse formation and then cluster at developing synapses between hippocampal neurons. N-cadherin is expressed initially at all synaptic sites but rapidly becomes restricted to a subpopulation of excitatory synaptic sites. Sites of GABAergic, inhibitory synapses in mature cultures therefore lack N-cadherin but are associated with clusters of beta-catenin, implying that they contain a different classic cadherin. These findings indicate that N-cadherin adhesion may stabilize early synapses that can then be remodeled to express a different cadherin and that cadherins systematically differentiate between functionally (excitatory and inhibitory) and spatially distinct synaptic sites on single neurons. These results suggest that differential cadherin expression may orchestrate the point-to-point specificity displayed by developing synapses.

Indexed as

Trans-ActivatorsAnimalsAntibody Specificitybeta CateninCadherinsCells, CulturedCytoskeletal Proteinsgamma-Aminobutyric AcidHippocampusNerve Tissue ProteinsNeural InhibitionNeuronsNuclear ProteinsRatsRats, Sprague-DawleySynapsesbeta CateninCadherinsCtnnb1 protein, ratCytoskeletal Proteinsgamma-Aminobutyric AcidNerve Tissue ProteinsNuclear ProteinsTrans-Activators

Identifiers

PMID9712659
PMCPMC6792987
OpenAlexW1912510903

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.