Evidence map›Paper›PMID 39422353›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2025

Osteopontin Promotes Cholangiocyte Secretion of Chemokines to Support Macrophage Recruitment and Fibrosis in MASH.

Jason D Coombes, Paul P Manka, Marzena Swiderska-Syn, Danielle T Vannan, Antonio Riva, Lee C Claridge, Cynthia Moylan, Ayako Suzuki, Marco A Briones-Orta, Rasha Younis and 14 more

Abstract read
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2025. 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
–field-weighted citation impact
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.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Myeloid cells in chronic liver inflammation.Cellular & molecular immunology · 2025
    Review
  9. Article
  10. Article
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

24 authors.

Jason D CoombesRegeneration and Repair, Institute of Hepatology, Foundation for Liver Research, London, UK.ORCID 0000-0002-5601-8977
Paul P MankaRegeneration and Repair, Institute of Hepatology, Foundation for Liver Research, London, UK.
Marzena Swiderska-SynDivision of Gastroenterology and Hepatology, School of Medicine, Saint Louis University, Saint Louis, Missouri, USA.
Danielle T VannanSnyder Institute for Chronic Diseases, University of Calgary, Calgary, Alberta, Canada.
Antonio RivaFaculty of Life Sciences and Medicine, King's College London, London, UK.ORCID 0000-0002-4974-2780
Lee C ClaridgeDepartment of Hepatology, Leeds Teaching Hospital NHS Trust, Leeds, UK.
Cynthia MoylanDivision of Gastroenterology, Department of Medicine, Duke University, Durham, North Carolina, USA.
Ayako SuzukiDivision of Gastroenterology, Department of Medicine, Duke University, Durham, North Carolina, USA.ORCID 0000-0003-1824-1067
Marco A Briones-OrtaRegeneration and Repair, Institute of Hepatology, Foundation for Liver Research, London, UK.
Rasha YounisRegeneration and Repair, Institute of Hepatology, Foundation for Liver Research, London, UK.
Naoto KitamuraRegeneration and Repair, Institute of Hepatology, Foundation for Liver Research, London, UK.
Svenja SydorGastroenterology and Hepatology, University Clinic Bochum, Bochum, Germany.ORCID 0000-0002-1349-8309
Shanna BittencourtLiver Cell Biology, Vrije Universiteit, Brussels, Belgium.
Zhiyong MiDepartment of Surgery, University of South Florida, Tampa, Florida, USA.
Paul C KuoDepartment of Surgery, University of South Florida, Tampa, Florida, USA.
Anna Mae DiehlDivision of Gastroenterology, Department of Medicine, Duke University, Durham, North Carolina, USA.
Leo A van GrunsvenLiver Cell Biology, Vrije Universiteit, Brussels, Belgium.ORCID 0000-0002-0990-7034
Shilpa ChokshiFaculty of Life Sciences and Medicine, King's College London, London, UK.
Ali CanbayGastroenterology and Hepatology, University Clinic Bochum, Bochum, Germany.ORCID 0000-0001-6069-7899
Manal F AbdelmalekDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.
Patricia AspichuetaDepartment of Physiology, Faculty of Medicine and Nursing, University of the Basque Country, EPV/EHU, Leioa, Spain.
Salvatore PapaLeeds Institute of Medical Research, St. James's University Hospital, University of Leeds, Leeds, UK.ORCID 0000-0002-8369-6538
Bertus EksteenSnyder Institute for Chronic Diseases, University of Calgary, Calgary, Alberta, Canada.
Wing-Kin SynRegeneration and Repair, Institute of Hepatology, Foundation for Liver Research, London, UK.

Funding

Hedgehog Signaling and Adult Liver RegenerationR01DK077794 · NIDDK · DUKE UNIVERSITY · PI DIEHL, ANNA MAE ELIZABETH · 2008 to 2020
$4.6M
Alberta InnovatesBelgian Federal Science Policy OfficeBRETCORE-UKDeutsche ForschungsgemeinschaftEuropean Association for the Study of the LiverFoundation for Liver ResearchGASLGuts UKIWT-FlandersNatural Sciences and Engineering Research Council of CanadaNIDDK NIH HHS R01 DK077794NIH HHSRégion de Bruxelles-CapitaleRosetrees TrustUniversity of BirminghamWilhelm Laupitz Foundation
6 · The paper itself

Abstract

BACKGROUND AND

aimsOsteopontin (OPN) promotes the ductular reaction and is a major driver of chronic liver disease (CLD) progression. Although CLD is characterised by the accumulation of inflammatory cells including macrophages around the peri-portal regions, the influence of OPN on recruitment is unclear. We investigated the role of OPN in cholangiocyte chemokine production and macrophage recruitment by combining in vivo, in vitro, and in silico approaches.

methodsThe effects of OPN on cholangiocyte chemokine production and macrophage migration were assessed in culture, alongside RNA-sequencing to identify genes and pathways affected by OPN depletion. Murine liver injury models were used to assess liver chemokine expression and liver macrophage/monocyte recruitment. OPN and chemokine expression were analysed in liver tissue and plasma from biopsy-proven metabolic dysfunction-associated alcoholic steatohepatitis (MASH) patients.

resultsOPN-knockdown in cholangiocytes reduced chemokine secretion. RNA-sequencing showed OPN-related effects clustered around immunity, chemotaxis and chemokine production. Macrophage exposure to cholangiocyte-conditioned media showed OPN-supported migration via chemokines chemokine (C-C motif) ligand (CCL)2, CCL5 and chemokine (C-X-C motif) ligand (CXCL)1. These effects were related to NF-κB signalling. Murine liver fibrosis was accompanied by upregulated liver OPN, CCL2, CCL5 and CXCL1 mRNA, and accumulation of liver cluster of differentiation (CD)11b/F4/80

conclusionsOPN promotes cholangiocyte chemokine secretion and the accumulation of pro-inflammatory monocytes. These data support neutralisation of OPN as an anti-inflammatory and anti-fibrotic strategy.

Indexed as

ChemokinesLiver CirrhosisMacrophagesOsteopontinAnimalsBile DuctsChemokine CCL2Chemokine CCL5Chemokine CXCL1Disease Models, AnimalHumansLiverMaleMiceMice, Inbred C57BLChemokine CCL2Chemokine CCL5Chemokine CXCL1ChemokinesOsteopontinSPP1 protein, humanSpp1 protein, mousechemokinecholangiocytefibrosismacrophageMASHosteopontin

Identifiers

PMID39422353
PMCPMC11893260

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Registered trials

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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.