Evidence map›Paper›PMID 28096298›Full record

ArticleJournal of leukocyte biology2017

MFG-E8-derived peptide attenuates adhesion and migration of immune cells to endothelial cells.

Yohei Hirano, Weng-Lang Yang, Monowar Aziz, Fangming Zhang, Barbara Sherry, Ping Wang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Yohei HiranoCenter for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, New York, USA.
Weng-Lang YangCenter for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, New York, USA.
Monowar AzizCenter for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, New York, USA.
Fangming ZhangCenter for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, New York, USA.
Barbara SherryCenter for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, New York, USA.
Ping WangCenter for Immunology and Inflammation, The Feinstein Institute for Medical Research, Manhasset, New York, USA; pwang@northwell.edu.
Feinstein Institute for Medical Research · USHofstra University · USJuntendo University Urayasu Hospital · JP

Funding

Targeting cognitive and immune impairment in sepsis survivorsP01AI102852 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI VOLPE, BRUCE THOMAS · 2014 to 2018
$11.5M
SEPSIS--MEDIATORS AND CARDIOVASCULAR RESPONSESR01GM057468 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, PING · 1998 to 2015
$3.8M
Modulation of Hepatocellular Function in SepsisR01GM053008 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, PING · 2001 to 2015
$3.7M
MODULATION OF HEPATOCELLULAR FUNCTION IN EARLY SEPSISR29GM053008 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, PING · 1995 to 2000
$41k
NIAID NIH HHS P01 AI102852NIGMS NIH HHS R01 GM053008NIGMS NIH HHS R01 GM057468NIGMS NIH HHS R29 GM053008
6 · The paper itself

Abstract

Milk fat globule-epidermal growth factor-factor 8 (MFG-E8) plays an immunomodulatory role in inflammatory diseases. MFG-E8-derived short peptide (MSP68) greatly reduces neutrophil infiltration and injury in the lung during sepsis. In this study, we examined the effect of MSP68 on chemotaxis of various immune cells and its regulatory mechanism. Bone marrow-derived neutrophils (BMDNs) from C57BL/6 mice, human monocyte THP-1 cell line, and human T lymphocyte Jurkat cell line were used for adhesion and migration assays using a Transwell method in the presence of MSP68. Treatment with MSP68 significantly inhibited the BMDN and THP-1 cell but not Jurkat cell adhesion on the TNF-α-stimulated pulmonary artery endothelial cell (PAEC) monolayer dose-dependently. MSP68 also significantly reduced BMDN adhesion on VCAM-1-coated wells dose dependently. Surface plasmon resonance (SPR) analysis revealed that MSP68 efficiently recognized integrin α

Indexed as

AnimalsAntigens, SurfaceCell AdhesionCell MovementCoculture TechniquesComplement C5aDiffusion Chambers, CultureEndothelial CellsGene Expression RegulationHumansIntegrin alpha4beta1Jurkat CellsMaleMiceMice, Inbred C57BLMilk ProteinsAntigens, SurfaceComplement C5aIntegrin alpha4beta1MFGE8 protein, humanMilk ProteinsPeptidesTumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1ICAM-1Mac-1p38VCAM-1VLA-4

Identifiers

PMID28096298
PMCPMC5380373
OpenAlexW2574117652

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.