Evidence map›Paper›PMID 10823888›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Regulation of the actin cycle in vivo by actin filament severing.

J L McGrath, E A Osborn, Y S Tardy, C F Dewey, J H Hartwig

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 101 citations in OpenAlex.

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  15. Secretion ofFrontiers in microbiology · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

J L McGrathHematology Division, Brigham and Women's Hospital, Boston, MA 02115, USA. jmcgrath@bme.jhu.edu
E A Osborn
Y S Tardy
C F Dewey
J H Hartwig
Massachusetts Institute of Technology · USBrigham and Women's Hospital · USÉcole Polytechnique Fédérale de Lausanne · CH

Funding

ACTIN DYNAMICS IN VASCULAR ENDOTHELIUMR01HL054145 · NHLBI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI DEWEY, C FORBES · 1996 to 2004
$1.3M
NHLBI NIH HHS HL54145NHLBI NIH HHS R01 HL054145
6 · The paper itself

Abstract

Cycling of actin subunits between monomeric and filamentous phases is essential for cell crawling behavior. We investigated actin filament turnover rates, length, number, barbed end exposure, and binding of cofilin in bovine arterial endothelial cells moving at different speeds depending on their position in a confluent monolayer. Fast-translocating cells near the wound edge have short filament lifetimes compared with turnover values that proportionately increase in slower moving cells situated at increasing distances from the wound border. Contrasted with slow cells exhibiting slow actin filament turnover speeds, fast cells have less polymerized actin, shorter actin filaments, more free barbed ends, and less actin-associated cofilin. Cultured primary fibroblasts manifest identical relationships between speed and actin turnover as the endothelial cells, and fast fibroblasts expressing gelsolin have higher actin turnover rates than slow fibroblasts that lack this actin-severing protein. These results implicate actin filament severing as an important control mechanism for actin cycling in cells.

Indexed as

Actin Depolymerizing FactorsActinsAdenosine DiphosphateAnimalsCattleCells, CulturedFluorescenceMicrofilament ProteinsActin Depolymerizing FactorsActinsAdenosine DiphosphateMicrofilament Proteins

Identifiers

PMID10823888
PMCPMC18648
OpenAlexW1977019885

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.