Evidence map›Paper›PMID 25355948›Full record

ArticleMolecular biology of the cell2014

Endothelial cells use dynamic actin to facilitate lymphocyte transendothelial migration and maintain the monolayer barrier.

Olivia L Mooren, Jinmei Li, Julie Nawas, John A Cooper

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 51 citations in OpenAlex.

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  8. Identifying novel mechanisms of abdominal aortic aneurysmFrontiers in cardiovascular medicine · 2022
    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.

Olivia L MoorenDepartment of Cell Biology and Physiology, Washington University, St. Louis, MO 63110.
Jinmei LiDepartment of Cell Biology and Physiology, Washington University, St. Louis, MO 63110.
Julie NawasDepartment of Cell Biology and Physiology, Washington University, St. Louis, MO 63110.
John A CooperDepartment of Cell Biology and Physiology, Washington University, St. Louis, MO 63110 jcooper@wustl.edu.
Washington University in St. Louis · US

Funding

Molecular Mechanisms in Actin Assembly &Cell MotilityR01GM038542 · NIGMS · WASHINGTON UNIVERSITY · PI COOPER, JOHN A · 1989 to 2013
$7.4M
Coordinate Regulation of the Actin Cytoskeleton and Membranes by DynaminF32GM083538 · NIGMS · WASHINGTON UNIVERSITY · PI MOOREN, OLIVIA L. · 2008 to 2010
$149k
MOLECULAR ANALYSIS OF CHROMOSOMAL TRANSLOCATIONSF32CA009184 · NCI · STANFORD UNIVERSITY · PI HUNGER, STEPHEN P · 1991 to 1993
–
NCI NIH HHS P30 CA09184NIGMS NIH HHS F32 GM083538NIGMS NIH HHS R01 GM038542NIGMS NIH HHS R01 GM 38542
6 · The paper itself

Abstract

The vascular endothelium is a highly dynamic structure, and the integrity of its barrier function is tightly regulated. Normally impenetrable to cells, the endothelium actively assists lymphocytes to exit the bloodstream during inflammation. The actin cytoskeleton of the endothelial cell (EC) is known to facilitate transmigration, but the cellular and molecular mechanisms are not well understood. Here we report that actin assembly in the EC, induced by Arp2/3 complex under control of WAVE2, is important for several steps in the process of transmigration. To begin transmigration, ECs deploy actin-based membrane protrusions that create a cup-shaped docking structure for the lymphocyte. We found that docking structure formation involves the localization and activation of Arp2/3 complex by WAVE2. The next step in transmigration is creation of a migratory pore, and we found that endothelial WAVE2 is needed for lymphocytes to follow a transcellular route through an EC. Later, ECs use actin-based protrusions to close the gap behind the lymphocyte, which we discovered is also driven by WAVE2. Finally, we found that ECs in resting endothelial monolayers use lamellipodial protrusions dependent on WAVE2 to form and maintain contacts and junctions between cells.

Indexed as

Transendothelial and Transepithelial MigrationActin CytoskeletonActin-Related Protein 2-3 ComplexActinsCapillary PermeabilityCells, CulturedElectric ImpedanceEndothelial CellsEndothelium, VascularHumansLymphocytesProtein TransportWiskott-Aldrich Syndrome Protein FamilyActin-Related Protein 2-3 ComplexActinsWASF2 protein, humanWiskott-Aldrich Syndrome Protein Family

Identifiers

PMID25355948
PMCPMC4263454
OpenAlexW2105049937

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.