Evidence map›Paper›PMID 26325534›Full record

ArticleJournal of hepatology2016

Hepatocyte tissue factor contributes to the hypercoagulable state in a mouse model of chronic liver injury.

Pierre-Emmanuel Rautou, Kohei Tatsumi, Silvio Antoniak, A Phillip Owens, Erica Sparkenbaugh, Lori A Holle, Alisa S Wolberg, Anna K Kopec, Rafal Pawlinski, James P Luyendyk and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hepatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Albumin promoter-driven FlpO expression induces efficient genetic recombination in mouse liver.American journal of physiology. Gastrointestinal and liver physiology · 2024
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  14. Caspase Inhibition Reduces Hepatic Tissue Factor-Driven Coagulation In Vitro and In Vivo.Toxicological sciences : an official journal of the Society of Toxicology · 2018
    Article
  15. Biology of portal hypertension.Hepatology international · 2018
    Review
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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

11 authors at 2 institutions in 2 countries.

Pierre-Emmanuel RautouDepartment of Medicine, Division of Hematology and Oncology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Service d'Hépatologie, Hôpital Beaujon, Assistance Publique-Hôpitaux de Paris, Clichy, France. Electronic address: pierre-emmanuel.rautou@inserm.fr.
Kohei TatsumiDepartment of Medicine, Division of Hematology and Oncology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Silvio AntoniakDepartment of Medicine, Division of Hematology and Oncology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
A Phillip OwensDepartment of Medicine, Division of Hematology and Oncology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Erica SparkenbaughDepartment of Medicine, Division of Hematology and Oncology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Lori A HolleDepartment of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Alisa S WolbergDepartment of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Anna K KopecDepartment of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, MI, USA.
Rafal PawlinskiDepartment of Medicine, Division of Hematology and Oncology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
James P LuyendykDepartment of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, MI, USA.
Nigel MackmanDepartment of Medicine, Division of Hematology and Oncology, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
University of North Carolina at Chapel Hill · USMichigan State University · US

Funding

The Impact of Tobacco Exposure on the Lungs Innate Defense SystemP50HL120100 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GLISH, GARY L · 2013 to 2017
$21.0M
Research Training in Hematology at UNC Chapel HillT32HL007149 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Nigel S. Key · 1985 to 2026
$8.6M
Fibrinogen and Factor XIII in Venous ThrombosisR01HL126974 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Alisa S. Wolberg · 2016 to 2026
$4.4M
Novel anti-fibrotic mechanisms in chemical-induced liver injuryR01ES017537 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI LUYENDYK, JAMES P · 2009 to 2019
$3.6M
Mechanisms of Venous Thromboembolism in CancerR01HL095096 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KEY, NIGEL S., MACKMAN, NIGEL · 2008 to 2012
$2.6M
The Role of Tissue Factor: FVIIa-PAR-2 Signaling in Heart Ischemia/ReperfusionR01HL096679 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PAWLINSKI, RAFAL L · 2011 to 2015
$1.8M
Tissue Factor & Clot Formation In Abdominal Aortic AneurysmR00HL116786 · NHLBI · UNIVERSITY OF CINCINNATI · PI OWENS III, ALBERT PHILLIP · 2015 to 2017
$736k
Determinants of Thrombus Structure and StabilityR56HL094740 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WOLBERG, ALISA S. · 2014 to 2014
$378k
OXPAPC induction of Tissue FactorF32HL099175 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI OWENS III, ALBERT PHILLIP · 2010 to 2012
$134k
NHLBI NIH HHS 1F32-HL099175-03NHLBI NIH HHS F32 HL099175NHLBI NIH HHS HL095096NHLBI NIH HHS P50 HL120100NHLBI NIH HHS P50HL120100NHLBI NIH HHS R00 HL116786NHLBI NIH HHS R01 HL095096NHLBI NIH HHS R01 HL096679NHLBI NIH HHS R01 HL126974NHLBI NIH HHS R56 HL094740NHLBI NIH HHS T32 HL007149NHLBI NIH HHS T32-HL007149-37NIEHS NIH HHS ES017537NIEHS NIH HHS R01 ES017537
6 · The paper itself

Abstract

BACKGROUND &

aimsPatients with chronic liver disease and cirrhosis have a dysregulated coagulation system and are prone to thrombosis. The basis for this hypercoagulable state is not completely understood. Tissue factor (TF) is the primary initiator of coagulation in vivo. Patients with cirrhosis have increased TF activity in white blood cells and circulating microparticles. The aim of our study was to determine the contribution of TF to the hypercoagulable state in a mouse model of chronic liver injury.

methodsWe measured levels of TF activity in the liver, white blood cells and circulating microparticles, and a marker of activation of coagulation (thrombin-antithrombin complexes (TATc)) in the plasma of mice subjected to bile duct ligation for 12days. We used wild-type mice, mice with a global TF deficiency (low TF mice), and mice deficient for TF in either myeloid cells (TF(flox/flox),LysMCre mice) or in hepatocytes (TF(flox/flox),AlbCre).

resultsWild-type mice with liver injury had increased levels of white blood cell, microparticle TF activity and TATc compared to sham mice. Low TF mice and mice lacking TF in hepatocytes had reduced levels of TF in the liver and in microparticles and exhibited reduced activation of coagulation without a change in liver fibrosis. In contrast, mice lacking TF in myeloid cells had reduced white blood cell TF but no change in microparticle TF activity or TATc.

conclusionsHepatocyte TF activates coagulation in a mouse model of chronic liver injury. TF may contribute to the hypercoagulable state associated with chronic liver diseases in patients.

Indexed as

AnimalsCells, CulturedChronic DiseaseDisease Models, AnimalHepatocytesHumansLiver DiseasesMaleMiceMice, Inbred C57BLThrombophiliaThromboplastinThromboplastinCoagulationLiver injuryMicroparticleThrombosis

Identifiers

PMID26325534
PMCPMC4691429
OpenAlexW1217917714

What OpenQuestion holds

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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.