Evidence map›Paper›PMID 18550846›Full record

ArticleBlood2008

Separable requirements for cytoplasmic domain of PSGL-1 in leukocyte rolling and signaling under flow.

Jonathan J Miner, Lijun Xia, Tadayuki Yago, János Kappelmayer, Zhenghui Liu, Arkadiusz G Klopocki, Bojing Shao, J Michael McDaniel, Hendra Setiadi, David W Schmidtke and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 102 citations in OpenAlex.

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  20. Selectins in cancer immunity.Glycobiology · 2018
    Review

7 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Jonathan J MinerCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
Lijun Xia
Tadayuki Yago
János Kappelmayer
Zhenghui Liu
Arkadiusz G Klopocki
Bojing Shao
J Michael McDaniel
Hendra Setiadi
David W Schmidtke
Rodger P McEver
Oklahoma Medical Research Foundation · USUniversity of Oklahoma · USUniversity of Oklahoma Health Sciences Center · US

Funding

Protein-glycan Interactions in the Vascular SystemP01HL085607 · NHLBI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI CUMMINGS, RICHARD D, MCEVER, RODGER PAUL · 2006 to 2015
$16.8M
SWI/SNF-REGULATED POSTNATAL ANGIOGENESISP20RR018758 · NCRR · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI MCEVER, RODGER PAUL · 2003 to 2011
$14.9M
Signal-dependent neutrophil adhesion to vascular surfacesR01HL034363 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI MCEVER, RODGER PAUL · 1985 to 2017
$3.9M
CYTOPLASMIC REGULATION OF P-SELECTIN/PSGL-1 INTERACTIONSR37HL034363 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI MCEVER, RODGER PAUL · 1998 to 2007
$3.3M
NCRR NIH HHS P20 RR018758NCRR NIH HHS RR 018758NHLBI NIH HHS HL 085607NHLBI NIH HHS HL 34363NHLBI NIH HHS P01 HL085607NHLBI NIH HHS R01 HL034363NHLBI NIH HHS R37 HL034363
6 · The paper itself

Abstract

In inflamed venules, leukocytes use P-selectin glycoprotein ligand-1 (PSGL-1) to roll on P-selectin and E-selectin and to activate integrin alphaLbeta2 (lymphocyte function-associated antigen-1, LFA-1) to slow rolling on intercellular adhesion molecule-1 (ICAM-1). Studies in cell lines have suggested that PSGL-1 requires its cytoplasmic domain to localize in membrane domains, to support rolling on P-selectin, and to signal through spleen tyrosine kinase (Syk). We generated "DeltaCD" mice that express PSGL-1 without the cytoplasmic domain. Unexpectedly, neutrophils from these mice localized PSGL-1 normally in microvilli, uropods, and lipid rafts. DeltaCD neutrophils expressed less PSGL-1 on their surfaces because of inefficient export from the endoplasmic reticulum. Limited digestion of wild-type neutrophils with O-sialoglycoprotein endopeptidase was used to reduce the PSGL-1 density to that on DeltaCD neutrophils. At matched PSGL-1 densities, both DeltaCD and wild-type neutrophils rolled similarly on P-selectin. However, DeltaCD neutrophils rolling on P-selectin did not trigger Syk-dependent activation of LFA-1 to slow rolling on ICAM-1. These data demonstrate that the PSGL-1 cytoplasmic domain is dispensable for leukocyte rolling on P-selectin but is essential to activate beta2 integrins to slow rolling on ICAM-1.

Indexed as

Amino Acid SequenceAnimalsCD18 AntigensHemorheologyIntercellular Adhesion Molecule-1Intracellular Signaling Peptides and ProteinsIn Vitro TechniquesLeukocyte RollingMembrane GlycoproteinsMembrane MicrodomainsMiceMice, KnockoutMice, TransgenicMicrovilliModels, BiologicalModels, MolecularCD18 AntigensIcam1 protein, mouseIntercellular Adhesion Molecule-1Intracellular Signaling Peptides and ProteinsMembrane GlycoproteinsPeptide FragmentsProtein-Tyrosine KinasesP-SelectinP-selectin ligand proteinRecombinant ProteinsSyk KinaseSyk protein, mouse

Identifiers

PMID18550846
PMCPMC2518905
OpenAlexW2027414724

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.