Evidence map›Paper›PMID 18787414›Full record

ArticleCell cycle (Georgetown, Tex.)2008

Focal adhesion components are essential for mammalian cell cytokinesis.

Sasha H Shafikhani, Keith Mostov, Joanne Engel

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  13. Cell migration regulates the kinetics of cytokinesis.Cell cycle (Georgetown, Tex.) · 2011
    Article
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  15. 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

3 authors at 1 institution in 1 country.

Sasha H ShafikhaniDepartment of Medicine, University of California, San Francisco, California, USA.
Keith Mostov
Joanne Engel
University of California, San Francisco · US

Funding

Sulfs and Injury Repair in Mucosal EpitheliaP01AI053194 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSEN, STEVEN D · 2002 to 2012
$13.4M
MECHANISM OF PSEUDOMONAS MEDIATED EPITHELIAL CELL DAMAGER01AI042806 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ENGEL, JOANNE N. · 1998 to 2010
$4.6M
Pseudomonas aeruginosa-induced host cell pathogenesisF32AI054056 · NIAID · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI SHAFIKHANI, SASHA H · 2003 to 2005
$147k
NIAID NIH HHS F32 AI054056NIAID NIH HHS P01 AI053194NIAID NIH HHS R01 AI042806NIAID NIH HHS R01 AI053194NIAID NIH HHS R01 AI42806
6 · The paper itself

Abstract

The final stages in mammalian cytokinesis are poorly understood. Previously, we reported that the ADP-ribosyltransferase activity of Pseudomonas aeruginosa type III secreted toxin ExoT inhibits late stages of cytokinesis. Given that Crk adaptor proteins are the major substrates of ExoT ADP-ribosyltransferase activity, we tested the involvement of Crk in cytokinesis. We report that the focal adhesion-associated proteins, Crk and paxillin are essential for completion of cytokinesis. When their function is absent, the cytoplasmic bridge fails to resolve and the daughter cells fuse to form a binucleated cell. During cytokinesis, Crk is required for syntaxin-2 recruitment to the midbody, while paxillin is required for both Crk and syntaxin-2 localization to this compartment. Our data demonstrate that the subcellular localization and the activity of RhoA and citron K, which are essential for early stages of cytokinesis, are not dependent on paxillin, Crk or syntaxin-2. These studies reveal a novel role for Crk and paxillin in cytokinesis and suggest that focal adhesion complex, as a unit, may partake in this fundamental cellular process.

Indexed as

CytokinesisAnimalsCell Line, TransformedFocal AdhesionsGenes, DominantHeLa CellsHumansMammalsPaxillinProtein IsoformsProtein Structure, TertiaryProtein TransportProto-Oncogene Proteins c-crkProto-Oncogene Proteins pp60(c-src)Syntaxin 1CRK protein, humanPaxillinProtein IsoformsProto-Oncogene Proteins c-crkProto-Oncogene Proteins pp60(c-src)Syntaxin 1

Identifiers

PMID18787414
PMCPMC2745397
OpenAlexW2093836108

What OpenQuestion holds

Textmetadata
LicenceTDM
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.