Evidence map›Paper›PMID 26078290›Full record

ArticleGut2016

CD248/endosialin critically regulates hepatic stellate cell proliferation during chronic liver injury via a PDGF-regulated mechanism.

Annika Wilhelm, Victoria Aldridge, Debashis Haldar, Amy J Naylor, Christopher J Weston, Ditte Hedegaard, Abhilok Garg, Janine Fear, Gary M Reynolds, Adam P Croft and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Deletion of Cd248 inJournal of molecular and cellular cardiology plus · 2026
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2 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

13 authors at 5 institutions in 1 country.

Annika WilhelmNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK.
Victoria AldridgeNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK University Hospital Birmingham NHS Foundation Trust, Birmingham, UK.
Debashis HaldarNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK.
Amy J NaylorCentre for Translational Inflammation Research, University of Birmingham, Birmingham, West Midlands, UK.
Christopher J WestonNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK.
Ditte HedegaardNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK.
Abhilok GargNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK.
Janine FearNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK.
Gary M ReynoldsNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK.
Adam P CroftCentre for Translational Inflammation Research, University of Birmingham, Birmingham, West Midlands, UK.
Neil C HendersonMRC Centre for Inflammation Research, University of Edinburgh, Edinburgh, UK.
Christopher D BuckleyCentre for Translational Inflammation Research, University of Birmingham, Birmingham, West Midlands, UK.
Philip N NewsomeNIHR Birmingham Liver BRU and Centre for Liver Research, University of Birmingham, Birmingham, UK University Hospital Birmingham NHS Foundation Trust, Birmingham, UK.
NIHR Birmingham Liver Biomedical Research Unit · GBUniversity of Birmingham · GBBirmingham City University · GBCentre for Inflammation Research · GBUniversity of Edinburgh · GB

Funding

Medical Research Council MR/L022699/1Versus Arthritis 19791Wellcome TrustWellcome Trust 103749/Z/14/ZWellcome Trust WT104551AIA
6 · The paper itself

Abstract

introductionCD248 (endosialin) is a stromal cell marker expressed on fibroblasts and pericytes. During liver injury, myofibroblasts are the main source of fibrotic matrix.

objectiveTo determine the role of CD248 in the development of liver fibrosis in the rodent and human setting.

designCD248 expression was studied by immunostaining and quantitative PCR in both normal and diseased human and murine liver tissue and isolated hepatic stellate cells (HSCs). Hepatic fibrosis was induced in CD248(-/-) and wild-type controls with carbon tetrachloride (CCl4) treatment.

resultsExpression of CD248 was seen in normal liver of humans and mice but was significantly increased in liver injury using both immunostaining and gene expression assays. CD248 was co-expressed with a range of fibroblast/HSC markers including desmin, vimentin and α-smooth muscle actin (α-SMA) in murine and human liver sections. CD248 expression was restricted to isolated primary murine and human HSC. Collagen deposition and α-SMA expression, but not inflammation and neoangiogenesis, was reduced in CD248(-/-) mice compared with wild-type mice after CCl4 treatment. Isolated HSC from wild-type and CD248(-/-) mice expressed platelet-derived growth factor receptor α (PDGFR-α) and PDGFR-β at similar levels. As expected, PDGF-BB stimulation induced proliferation of wild-type HSC, whereas CD248(-/-) HSC did not demonstrate a proliferative response to PDGF-BB. Abrogated PDGF signalling in CD248(-/-) HSC was confirmed by significantly reduced c-fos expression in CD248(-/-) HSC compared with wild-type HSC.

conclusionsOur data show that deletion of CD248 reduces susceptibility to liver fibrosis via an effect on PDGF signalling, making it an attractive clinical target for the treatment of liver injury.

Indexed as

ActinsAngiogenesis Inducing AgentsAnimalsAntigens, CDAntigens, NeoplasmBecaplerminCarbon TetrachlorideCell ProliferationCells, CulturedChemical and Drug Induced Liver InjuryChronic DiseaseCollagenDesminFibrosisGene ExpressionHepatic Stellate CellsACTA2 protein, humanActinsalpha-smooth muscle actin, mouseAngiogenesis Inducing AgentsAntigens, CDAntigens, NeoplasmBecaplerminCarbon TetrachlorideCD248 protein, humanCD248 protein, mouseCollagenDesminPlatelet-Derived Growth FactorProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaRNA, MessengerTransforming Growth Factor betaVimentinFIBROSISHEPATIC STELLATE CELLMYOFIBROBLASTS

Identifiers

PMID26078290
PMCPMC4941145
OpenAlexW2107898368

What OpenQuestion holds

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LicenceCC BY
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.