Evidence map›Paper›PMID 22437826›Full record

ArticleThe Journal of biological chemistry2012

Mechanism of evenness interrupted (Evi)-exosome release at synaptic boutons.

Kate Koles, John Nunnari, Ceren Korkut, Romina Barria, Cassandra Brewer, Yihang Li, John Leszyk, Bing Zhang, Vivian Budnik

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 178 papers.

0numbers the graph read from it
0cells of the map it votes in
178citing papers in PubMed
8.6field-weighted citation impact, top 1% 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

178 citing papers in PubMed, 280 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Extracellular vesicles inEXO : beyond the cell · 2026
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Isolation of extracellular vesicles from insect hemolymph.Current research in insect science · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

118 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

9 authors at 2 institutions in 1 country.

Kate KolesDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA. kate.koles@umassmed.edu
John Nunnari
Ceren Korkut
Romina Barria
Cassandra Brewer
Yihang Li
John Leszyk
Bing Zhang
Vivian Budnik
University of Massachusetts Chan Medical School · USUniversity of Oklahoma · US

Funding

The Wingless Transduction Pathway in Synapse DevelopmentR01MH070000 · NIMH · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BUDNIK, VIVIAN G. · 2004 to 2013
$3.6M
NIMH NIH HHS R01 MH070000NIMH NIH HHS R01 MH0700000NINDS NIH HHS R01 NS06878
6 · The paper itself

Abstract

Wnt signaling plays critical roles during synaptic development and plasticity. However, the mechanisms by which Wnts are released and travel to target cells are unresolved. During synaptic development, the secretion of Drosophila Wnt1, Wingless, requires the function of Evenness Interrupted (Evi)/Wls, a Wingless-binding protein that is secreted along with Wingless at the neuromuscular junction. Given that Evi is a transmembrane protein, these studies suggested the presence of a novel vesicular mechanism of trans-synaptic communication, potentially in the form of exosomes. To establish the mechanisms for the release of Evi vesicles, we used a dsRNA assay in cultured cells to screen for genes that when down-regulated prevent the release of Evi vesicles. We identified two proteins, Rab11 and Syntaxin 1A (Syx1A), that were required for Evi vesicle release. To determine whether the same mechanisms were used in vivo at the neuromuscular junction, we altered the activity of Rab11 and Syx1A in motoneurons and determined the impact on Evi release. We found that Syx1A, Rab11, and its effector Myosin5 were required for proper Evi vesicle release. Furthermore, ultrastructural analysis of synaptic boutons demonstrated the presence of multivesicular bodies, organelles involved in the production and release of exosomes, and these multivesicular bodies contained Evi. We also used mass spectrometry, electron microscopy, and biochemical techniques to characterize the exosome fraction from cultured cells. Our studies revealed that secreted Evi vesicles show remarkable conservation with exosomes in other systems. In summary, our observations unravel some of the in vivo mechanisms required for Evi vesicle release.

Indexed as

AnimalsBiological TransportDrosophila melanogasterDrosophila ProteinsExosomesIntracellular Signaling Peptides and ProteinsMembrane ProteinsMyosin Type VNeuromuscular Junctionrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsSynaptic TransmissionSynaptic VesiclesDrosophila ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsMyosin Type Vrab11 GTP-Binding ProteinsRab11 protein, Drosophilarab GTP-Binding ProteinsWls protein, Drosophila

Identifiers

PMID22437826
PMCPMC3351299
OpenAlexW2020498762

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.