Evidence map›Paper›PMID 25822334›Full record

ArticlePloS one2015

Establishment and characterization of rat portal myofibroblast cell lines.

Michel Fausther, Jessica R Goree, Élise G Lavoie, Alicia L Graham, Jean Sévigny, Jonathan A Dranoff

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Working with Immortalized Hepatic Stellate Cell Lines.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  8. Cancer-Associated Fibroblasts in Hepatocellular Carcinoma and Cholangiocarcinoma.Cellular and molecular gastroenterology and hepatology · 2023
    Review
  9. Article
  10. Cellular Mechanisms of Liver Fibrosis.Frontiers in pharmacology · 2021
    Review
  11. Review
  12. Review
  13. Mechanisms of liver fibrosis and its role in liver cancer.Experimental biology and medicine (Maywood, N.J.) · 2020
    Review
  14. Article
  15. Review
  16. Article
  17. Hepatic stellate cells as key target in liver fibrosis.Advanced drug delivery reviews · 2017
    Review
  18. Article
  19. Review
  20. 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

6 authors at 3 institutions in 2 countries.

Michel FaustherDivision of Gastroenterology & Hepatology, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America; Research Service, Central Arkansas VA Healthcare System, Little Rock, AR, United States of America.
Jessica R GoreeDivision of Gastroenterology & Hepatology, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America; Research Service, Central Arkansas VA Healthcare System, Little Rock, AR, United States of America.
Élise G LavoieDivision of Gastroenterology & Hepatology, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America; Research Service, Central Arkansas VA Healthcare System, Little Rock, AR, United States of America.
Alicia L GrahamDivision of Gastroenterology & Hepatology, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America.
Jean SévignyDépartement de Microbiologie-Infectiologie et d'Immunologie, Faculté de Médecine, Université Laval, QC, Canada; Centre de Recherche du CHU de Québec, QC, Canada.
Jonathan A DranoffDivision of Gastroenterology & Hepatology, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America; Research Service, Central Arkansas VA Healthcare System, Little Rock, AR, United States of America.
University of Arkansas for Medical Sciences · USCentral Arkansas Veterans Healthcare System · USUniversité Laval · CA

Funding

Arkansas Center for Clinical and Translational ResearchUL1TR000039 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI BECK, CORNELIA MARIE, JAMES, LAURA P · 2012 to 2014
$10.0M
Regulation of Bile Ductular ProliferationR01DK070849 · NIDDK · YALE UNIVERSITY · PI DRANOFF, JONATHAN A · 2005 to 2009
$1.6M
Pathogenesis of Biliary CirrhosisR56DK070849 · NIDDK · YALE UNIVERSITY · PI DRANOFF, JONATHAN A · 2010 to 2010
$386k
Canadian Institutes of Health Research MOP-102472NCATS NIH HHS UL1 TR000039NCATS NIH HHS UL1TR000039NIDDK NIH HHS R01 DK070849NIDDK NIH HHS R56 DK070849
6 · The paper itself

Abstract

The major sources of scar-forming myofibroblasts during liver fibrosis are activated hepatic stellate cells (HSC) and portal fibroblasts (PF). In contrast to well-characterized HSC, PF remain understudied and poorly defined. This is largely due to the facts that isolation of rodent PF for functional studies is technically challenging and that PF cell lines had not been established. To address this, we have generated two polyclonal portal myofibroblast cell lines, RGF and RGF-N2. RGF and RGF-N2 were established from primary PF isolated from adult rat livers that underwent culture activation and subsequent SV40-mediated immortalization. Specifically, Ntpdase2/Cd39l1-sorted primary PF were used to generate the RGF-N2 cell line. Both cell lines were functionally characterized by RT-PCR, immunofluorescence, immunoblot and bromodeoxyuridine-based proliferation assay. First, immortalized RGF and RGF-N2 cells are positive for phenotypic myofibroblast markers alpha smooth muscle actin, type I collagen alpha-1, tissue inhibitor of metalloproteinases-1, PF-specific markers elastin, type XV collagen alpha-1 and Ntpdase2/Cd39l1, and mesenchymal cell marker ecto-5'-nucleotidase/Cd73, while negative for HSC-specific markers desmin and lecithin retinol acyltransferase. Second, both RGF and RGF-N2 cell lines are readily transfectable using standard methods. Finally, RGF and RGF-N2 cells attenuate the growth of Mz-ChA-1 cholangiocarcinoma cells in co-culture, as previously demonstrated for primary PF. Immortalized rat portal myofibroblast RGF and RGF-N2 cell lines express typical markers of activated PF-derived myofibroblasts, are suitable for DNA transfection, and can effectively inhibit cholangiocyte proliferation. Both RGF and RGF-N2 cell lines represent novel in vitro cellular models for the functional studies of portal (myo)fibroblasts and their contribution to the progression of liver fibrosis.

Indexed as

Cell LineAnimalsBiomarkersBromodeoxyuridineCell Culture TechniquesFluorescent Antibody TechniqueImmunoblottingLiverMyofibroblastsPortal SystemRatsReverse Transcriptase Polymerase Chain ReactionBiomarkersBromodeoxyuridine

Identifiers

PMID25822334
PMCPMC4378927
OpenAlexW2087948920

What OpenQuestion holds

Textmetadata
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.