Evidence map›Paper›PMID 6684662›Full record

ArticleThe Journal of cell biology1983

Subcellular distribution of rhodamine-actin microinjected into living fibroblastic cells.

S D Glacy

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1983. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.8field-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

21 citing papers in PubMed, 53 citations in OpenAlex.

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  6. Thymosin beta 4 (Fx peptide) is a potent regulator of actin polymerization in living cells.Proceedings of the National Academy of Sciences of the United States of America · 1992
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  17. Treadmilling, diffusional exchange and cytoplasmic structures.Journal of muscle research and cell motility · 1985
    Review
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  20. Review
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

1 author.

S D Glacy

Funding

MECHANISMS OF CYTOKINESIS IN ANIMAL CELLSR01HD007193 · NICHD · KANSAS STATE UNIVERSITY · PI CONRAD, GARY W · 1985 to 1986
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NICHD NIH HHS HD-07193
6 · The paper itself

Abstract

The time course and pattern of incorporation of rhodamine-labeled actin microinjected into cultured fibroblastic cells were examined by fluorescence microscopy. Following microinjection, the fluorescent probe was incorporated rapidly into ruffling membranes, and within 5 min faintly fluorescent stress fibers were observed. Levels of fluorescence in ruffling membranes then tended to remain constant while fluorescence of the stress fibers continued to increase until approximately 20-min postinjection. Small, discrete regions of some microinjected cells displayed high levels of fluorescence that appeared initially approximately 5-10 min postinjection. I observed these small areas of intense fluorescence frequently near the cell periphery, which corresponded to focal contacts when examined with interference reflection optics. The results of this study show that a relationship exists between patterns of fluorescent actin incorporation in these cells and cellular areas or structures presumed to play a role in cell movement. These findings suggest that actin within stress fibers and the microfilament network of ruffling membranes undergoes a rapid turnover that may relate directly to the motility of the cell.

Indexed as

ActinsAnimalsCell MembraneCell MovementCells, CulturedChick EmbryoCytoplasmCytoskeletonFibroblastsKineticsMicroinjectionsMicroscopy, FluorescenceRhodaminesActinsRhodamines

Identifiers

PMID6684662
PMCPMC2112619
OpenAlexW2136970616

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.