Evidence map›Paper›PMID 3204122›Full record

ArticleThe Journal of cell biology1988

The dynamic distribution of fluorescent analogues of actin and myosin in protrusions at the leading edge of migrating Swiss 3T3 fibroblasts.

R L DeBiasio, L L Wang, G W Fisher, D L Taylor

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1988. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 101 citations in OpenAlex.

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  11. Keratocytes generate traction forces in two phases.Molecular biology of the cell · 1999
    Article
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  15. Myogenic cells express multiple myosin isoforms.Journal of muscle research and cell motility · 1997
    Article
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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

4 authors at 1 institution in 1 country.

R L DeBiasioDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213.
L L Wang
G W Fisher
D L Taylor
Carnegie Mellon University · US

Funding

APPLICATIONS OF FLUORESCENCE TECHNIQUES IN CELL BIOLOGYP01GM034639 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI TAYLOR, D. LANSING · 1985 to 1989
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STRUCTURAL AND CHEMICAL DYNAMICS OF CELL MOVEMENTR01AM032461 · AM · CARNEGIE-MELLON UNIVERSITY · PI TAYLOR, D. LANSING · 1985 to 1985
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FLUORESCENCE MICROSCOPY BY DIGITAL IMAGE ANALYSISS10RR003377 · NCRR · CARNEGIE-MELLON UNIVERSITY · PI TAYLOR, D. LANSING · 1987 to 1987
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NCRR NIH HHS 1S10 RR03377NIADDK NIH HHS AM32461NIGMS NIH HHS GM34639
6 · The paper itself

Abstract

The formation of protrusions at the leading edge of the cell is an essential step in fibroblast locomotion. Using fluorescent analogue cytochemistry, ratio imaging, multiple parameter analysis, and fluorescence photobleaching recovery, the distribution of actin and myosin was examined in the same protrusions at the leading edge of live, locomoting cells during wound-healing in vitro. We have previously defined two temporal stages of the formation of protrusions: (a) initial protrusion and (b) established protrusion (Fisher et al., 1988). Actin was slightly concentrated in initial protrusions, while myosin was either totally absent or present at extremely low levels at the base of the initial protrusions. In contrast, established protrusions contained diffuse actin and actin microspikes, as well as myosin in both diffuse and structured forms. Actin and myosin were also localized along concave transverse fibers near the base of initial and established protrusions. The dynamics of myosin penetration into a relatively stable, established protrusion was demonstrated by recording sequential images over time. Myosin was shown to be absent from an initial protrusion, but diffuse and punctate myosin was detected in the same protrusion within 1-2 min. Fluorescence photobleaching recovery indicated that myosin was 100% immobile in the region behind the leading edge containing transverse fibers, in comparison to the 21% immobile fraction detected in the perinuclear region. Possible explanations of the delayed penetration of myosin into established protrusions and the implications on the mechanism of protrusion are discussed.

Indexed as

ActinsAnimalsCell LineCell MovementFibroblastsFluorescent DyesHistocytochemistryImage Processing, Computer-AssistedMicroinjectionsMyosinsActinsFluorescent DyesMyosins

Identifiers

PMID3204122
PMCPMC2115635
OpenAlexW1976138565

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.