Evidence map›Paper›PMID 23690179›Full record

ArticleThe Journal of cell biology2013

Live-cell imaging of exocyst links its spatiotemporal dynamics to various stages of vesicle fusion.

Felix Rivera-Molina, Derek Toomre

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Preassembly and independent trafficking of the exocyst complex inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Intracellular and Extracellular Vesicle miRNA Signatures in Human iPSC-Derived Neural Stem Cells and Floor Plate Progenitors.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  4. The exocyst in context.Biochemical Society transactions · 2024
    Review
  5. Emerging Roles of Exocyst Complex in Fungi: A Review.Journal of fungi (Basel, Switzerland) · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Use of Ecto-Tagged Integrins to Monitor Integrin Exocytosis and Endocytosis.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  10. Review
  11. Regulation of EGF-stimulated activation of the PI-3K/AKT pathway by exocyst-mediated exocytosis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Article
  13. Exocytosis in Astrocytes.Biomolecules · 2021
    Review
  14. Article
  15. Article
  16. The Golgi as a "Proton Sink" in Cancer.Frontiers in cell and developmental biology · 2021
    Article
  17. Review
  18. Review
  19. Article
  20. InducibleThe Journal of biological chemistry · 2019
    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

2 authors at 1 institution in 1 country.

Felix Rivera-MolinaDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA.
Derek Toomre
Yale University · US

Funding

Novel TIRF microscopy analyzing trafficking & signaling at the cell cortexDP2OD002980 · OD · YALE UNIVERSITY · PI TOOMRE, DEREK K. · 2007 to 2009
$2.5M
Dynamics of exocyst recruitment and assemblyR01GM098498 · NIGMS · YALE UNIVERSITY · PI TOOMRE, DEREK K. · 2013 to 2015
$1.0M
NIGMS NIH HHS R01 GM098498NIH HHS 1DP2OD002980NIH HHS DP2 OD002980Wellcome Trust
6 · The paper itself

Abstract

Tethers play ubiquitous roles in membrane trafficking and influence the specificity of vesicle attachment. Unlike soluble N-ethyl-maleimide-sensitive fusion attachment protein receptors (SNAREs), the spatiotemporal dynamics of tethers relative to vesicle fusion are poorly characterized. The most extensively studied tethering complex is the exocyst, which spatially targets vesicles to sites on the plasma membrane. By using a mammalian genetic replacement strategy, we were able to assemble fluorescently tagged Sec8 into the exocyst complex, which was shown to be functional by biochemical, trafficking, and morphological criteria. Ultrasensitive live-cell imaging revealed that Sec8-TagRFP moved to the cell cortex on vesicles, which preferentially originated from the endocytic recycling compartment. Surprisingly, Sec8 remained with vesicles until full dilation of the fusion pore, supporting potential coupling with SNARE fusion machinery. Fluorescence recovery after photobleaching analysis of Sec8 at cell protrusions revealed that a significant fraction was immobile. Additionally, Sec8 dynamically repositioned to the site of membrane expansion, suggesting that it may respond to local cues during early cell polarization.

Indexed as

Cell LineCell MembraneExocytosisFluorescence Recovery After PhotobleachingHeLa CellsHumansMembrane FusionMicroscopy, FluorescenceSNARE ProteinsVesicular Transport ProteinsEXOC4 protein, humanSNARE ProteinsVesicular Transport Proteins

Identifiers

PMID23690179
PMCPMC3664709
OpenAlexW2170761272

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.