Evidence map›Paper›PMID 24378633›Full record

ArticleJournal of visualized experiments : JoVE2013

Visualizing cytoplasmic flow during single-cell wound healing in Stentor coeruleus.

Mark Slabodnick, Bram Prevo, Peter Gross, Janet Sheung, Wallace Marshall

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. A role for theMolecular biology of the cell · 2026
    Article
  2. Article
  3. A role for thebioRxiv : the preprint server for biology · 2025
    Article
  4. Characterization of cellular wound resistance in the giant ciliatebioRxiv : the preprint server for biology · 2025
    Article
  5. Physical Forces in Regeneration of Cells and Tissues.Cold Spring Harbor perspectives in biology · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Methods for the Study of Regeneration in Stentor.Journal of visualized experiments : JoVE · 2018
    Article
  10. Microfluidic guillotine for single-cell wound repair studies.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. Review
  12. How nontraditional model systems can save us.Molecular biology of the cell · 2015
    Article
  13. Stentor coeruleus.Current biology : CB · 2014
    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

5 authors at 4 institutions in 3 countries.

Mark SlabodnickPhysiology Course, Marine Biological Laboratory.
Bram Prevo
Peter Gross
Janet Sheung
Wallace Marshall
Marine Biological Laboratory · USUniversity of California, San Francisco · USUniversity of Illinois Urbana-Champaign · USVrije Universiteit Amsterdam · NL

Funding

GENETICS OF EUCARYOTIC AND PROCARYOTIC ORGANISMST32GM007810 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ASHRAFI, KAVEH, NARLIKAR, GEETA J · 1985 to 2020
$15.1M
Pattern formation & regeneration in a single cellR01GM090305 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARSHALL, WALLACE · 2009 to 2013
$1.8M
NIGMS NIH HHS R01 GM090305NIGMS NIH HHS T32 GM007810
6 · The paper itself

Abstract

Although wound-healing is often addressed at the level of whole tissues, in many cases individual cells are able to heal wounds within themselves, repairing broken cell membrane before the cellular contents leak out. The giant unicellular organism Stentor coeruleus, in which cells can be more than one millimeter in size, have been a classical model organism for studying wound healing in single cells. Stentor cells can be cut in half without loss of viability, and can even be cut and grafted together. But this high tolerance to cutting raises the question of why the cytoplasm does not simply flow out from the size of the cut. Here we present a method for cutting Stentor cells while simultaneously imaging the movement of cytoplasm in the vicinity of the cut at high spatial and temporal resolution. The key to our method is to use a "double decker" microscope configuration in which the surgery is performed under a dissecting microscope focused on a chamber that is simultaneously viewed from below at high resolution using an inverted microscope with a high NA lens. This setup allows a high level of control over the surgical procedure while still permitting high resolution tracking of cytoplasm.

Indexed as

AnimalsCells, CulturedCiliophoraCytoplasmMicroscopyRegenerationSingle-Cell AnalysisWound Healing

Identifiers

PMID24378633
PMCPMC4110943
OpenAlexW2023756566

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.