Evidence map›Paper›PMID 23562154›Full record

ArticleCell reports2013

A single Aplysia neurotrophin mediates synaptic facilitation via differentially processed isoforms.

Stefan R Kassabov, Yun-Beom Choi, Kevin A Karl, Harshad D Vishwasrao, Craig H Bailey, Eric R Kandel

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  7. Postsynaptic effects ofLearning & memory (Cold Spring Harbor, N.Y.) · 2020
    Article
  8. Review
  9. Review
  10. Intermediate-term memory inLearning & memory (Cold Spring Harbor, N.Y.) · 2018
    Article
  11. Autocrine signaling by anProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  12. Anterograde and retrograde signaling by anProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  13. BDNF, Brain, and Regeneration: Insights from Zebrafish.International journal of molecular sciences · 2018
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Cell-Specific PKM Isoforms Contribute to the Maintenance of Different Forms of Persistent Long-Term Synaptic Plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  20. 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

6 authors at 3 institutions in 1 country.

Stefan R KassabovDepartment of Neuroscience, College of Physicians and Surgeons of Columbia University, New York State Psychiatric Institute, 1051 Riverside Drive, New York, NY 10032, USA. srk2110@columbia.edu
Yun-Beom Choi
Kevin A Karl
Harshad D Vishwasrao
Craig H Bailey
Eric R Kandel
Columbia University · USHoward Hughes Medical Institute · USNew York State Psychiatric Institute

Funding

Molecular Engineering Approach to Study Long Term Synaptic PlasticityR01NS060762 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2008 to 2011
$2.3M
Genomic Approaches to Deciphering Memory CircuitsR01MH097062 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE, KANDEL, ERIC R · 2012 to 2016
$2.0M
Howard Hughes Medical InstituteNIMH NIH HHS R01 MH097062NINDS NIH HHS R01 NS060762
6 · The paper itself

Abstract

Neurotrophins control the development and adult plasticity of the vertebrate nervous system. Failure to identify invertebrate neurotrophin orthologs, however, has precluded studies in invertebrate models, limiting our understanding of fundamental aspects of neurotrophin biology and function. We identified a neurotrophin (ApNT) and Trk receptor (ApTrk) in the mollusk Aplysia and found that they play a central role in learning-related synaptic plasticity. Blocking ApTrk signaling impairs long-term facilitation, whereas augmenting ApNT expression enhances it and induces the growth of new synaptic varicosities at the monosynaptic connection between sensory and motor neurons of the gill-withdrawal reflex. Unlike vertebrate neurotrophins, ApNT has multiple coding exons and exerts distinct synaptic effects through differentially processed and secreted splice isoforms. Our findings demonstrate the existence of bona fide neurotrophin signaling in invertebrates and reveal a posttranscriptional mechanism that regulates neurotrophin processing and the release of proneurotrophins and mature neurotrophins that differentially modulate synaptic plasticity.

Indexed as

Alternative SplicingAmino Acid SequenceAnimalsAplysiaBrain-Derived Neurotrophic FactorCells, CulturedCoculture TechniquesHEK293 CellsHumansMolecular Sequence DataMotor NeuronsNerve Growth FactorsNeuronal PlasticityPC12 CellsProtein IsoformsRatsBrain-Derived Neurotrophic FactorNerve Growth FactorsProtein IsoformsReceptor, trkASerotonin

Identifiers

PMID23562154
PMCPMC4045214
OpenAlexW1978802114

What OpenQuestion holds

Textmetadata
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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.