Evidence map›Paper›PMID 18720226›Full record

ReviewMicrocirculation (New York, N.Y. : 1994)2009

Neutrophil recruitment under shear flow: it's all about endothelial cell rings and gaps.

Pilar Alcaide, Scott Auerbach, Francis W Luscinskas

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Microcirculation (New York, N.Y. : 1994), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.3field-weighted citation impact, top 8% 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, 83 citations in OpenAlex.

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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Pilar AlcaideCenter for Excellence in Vascular Biology, Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Scott Auerbach
Francis W Luscinskas
Brigham and Women's Hospital · USHarvard University · US

Funding

VCAM-1 IN CHRONIC INFLAMMATORY AND IMMUNE PROCESSESP01HL036028 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MAYADAS, TANYA N · 1985 to 2013
$32.1M
MICROVASCULAR ENDOTHELIAL LYMPHOCYTE ADHESION UNDER FLOWR01HL053993 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LUSCINSKAS, FRANCIS W. · 1996 to 2009
$3.8M
Endothelial Adhesion Molecules and Leukocyte EgressF32HL086217 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI AUERBACH, SCOTT D · 2006 to 2008
$95k
NHLBI NIH HHS F32 HL086217NHLBI NIH HHS HL36028NHLBI NIH HHS HL53993NHLBI NIH HHS P01 HL036028NHLBI NIH HHS R01 HL053993
6 · The paper itself

Abstract

Leukocyte recruitment to tissues and organs is an essential component of host defense. The molecular mechanisms controlling this process are complex and remain under active investigation. The combination of biochemical techniques and live cell imaging using in vivo and in vitro flow-model approaches have shed light on several aspects of neutrophil transmigration through the vascular endothelial lining of blood vessels. Here, we focus on the role of adhesion molecule signaling in endothelial cells and their downstream targets during the process of transendothelial migration at cell-cell borders (paracellular transmigration). An emerging model involves the leukocyte beta2 integrin engagement of endothelial cell ICAM-1, which triggers integrin-ICAM-1 clustering (rings) and stabilizes leukocyte adhesion at cell-cell junctions. This step recruits nonreceptor tyrosine kinases that phosphorylate key tyrosine residues in the cytoplasmic tail of VE-cadherin, which destabilizes its linkage to catenins and the actin cytoskeleton, triggering the transient opening of VE-cadherin homodimers to form a gap in the cell junction, through which the neutrophil transmigrates. Interestingly, the signaling events that lead to neutrophil transmigration occur independently of shear flow in vitro.

Indexed as

Models, ImmunologicalActinsAnimalsAntigens, CDCadherin 5CadherinsCD18 AntigensCell AdhesionCytoskeletonEndothelium, VascularHumansIntercellular Adhesion Molecule-1Intercellular JunctionsNeutrophil InfiltrationNeutrophilsShear StrengthActinsAntigens, CDCadherin 5CadherinsCD18 AntigensIntercellular Adhesion Molecule-1

Identifiers

PMID18720226
PMCPMC2726622
OpenAlexW1969565659

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.