Evidence map›Paper›PMID 31101623›Full record

ArticleBlood2019

Plasmin-mediated fibrinolysis enables macrophage migration in a murine model of inflammation.

Lakmali Munasinghage Silva, Andrew Gary Lum, Collin Tran, Molly W Shaw, Zhen Gao, Matthew J Flick, Niki M Moutsopoulos, Thomas H Bugge, Eric S Mullins

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 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

9 authors at 3 institutions in 1 country.

Lakmali Munasinghage SilvaProteases and Tissue Remodeling Section and.ORCID 0000-0001-6282-2657
Andrew Gary LumOral Inflammation and Immunity Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD.
Collin TranProteases and Tissue Remodeling Section and.
Molly W ShawDivision of Hematology and.
Zhen GaoDivision of Hematology and.
Matthew J FlickDivision of Experimental Hematology, Cancer and Blood Diseases Institute, Cincinnati Children's Research Foundation, Cincinnati, OH; and.
Niki M MoutsopoulosOral Inflammation and Immunity Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD.
Thomas H BuggeProteases and Tissue Remodeling Section and.
Eric S MullinsDivision of Hematology and.ORCID 0000-0002-1544-9068
National Institutes of Health · USCincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · US

Funding

Cell surface serine proteases in development, tissue repair, and malignancyZIADE000699 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI BUGGE, THOMAS H · 2009 to 2025
$34.1M
NIDCR DIR Scientific Cores (Combined Technical Research Core)ZICDE000729 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI ABSHARI, MEHRNOOSH · 2009 to 2025
$31.7M
NIDCR Annual Reports - Veterinary Resources CoreZIGDE000740 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI DAVIDSON, LAUREN · 2012 to 2025
$11.7M
Thrombin-dependent mechanisms of pancreatic ductal adenocarcinoma diseaseR01CA211098 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FLICK, MATTHEW J. · 2017 to 2022
$2.2M
Mechanisms linking hemostatic factors and neuroinflammatorydiseaseR01NS107258 · NINDS · CINCINNATI CHILDRENS HOSP MED CTR · PI MULLINS, ERIC S · 2019 to 2023
$2.1M
Fibrin(ogen) control of metabolic inflammation and obesityR01DK112778 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FLICK, MATTHEW J. · 2019 to 2022
$1.5M
Mechanisms linking the hemostatic protease thrombin to arthritic diseaseR01AR056990 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI FLICK, MATTHEW J. · 2009 to 2013
$1.3M
Intramural NIH HHS ZIC DE000729Intramural NIH HHS ZIG DE000740NIDCR NIH HHS ZIC DE000729NIDCR NIH HHS ZIG DE000740
6 · The paper itself

Abstract

Efficient migration of macrophages to sites of inflammation requires cell surface-bound plasmin(ogen). Here, we investigated the mechanisms underlying the deficits of plasmin(ogen)-mediated macrophage migration in 2 models: murine thioglycollate-induced peritonitis and in vitro macrophage migration. As previously reported, macrophage migration into the peritoneal cavity of mice in response to thioglycollate was significantly impaired in the absence of plasminogen. Fibrin(ogen) deposition was noted in the peritoneal cavity in response to thioglycollate, with a significant increase in fibrin(ogen) in the plasminogen-deficient mice. Interestingly, macrophage migration was restored in plasminogen-deficient mice by simultaneous imposition of fibrinogen deficiency. Consistent with this in vivo finding, chemotactic migration of cultured macrophages through a fibrin matrix did not occur in the absence of plasminogen. The macrophage requirement for plasmin-mediated fibrinolysis, both in vivo and in vitro

Indexed as

Chemotaxis, LeukocyteFibrinolysisAnimalsBiomarkersDisease Models, AnimalDisease SusceptibilityFibrinogenFibrinolysinFluorescent Antibody TechniqueHumansImmunophenotypingInflammationLeukocyte CountMacrophagesMiceMice, KnockoutBiomarkersFibrinogenFibrinolysinPlasminogen

Identifiers

PMID31101623
PMCPMC6639982
OpenAlexW2946553245

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.