Evidence map›Paper›PMID 11904425›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Immortalization of a primate bipotent epithelial liver stem cell.

Jean-Etienne Allain, Ibrahim Dagher, Dominique Mahieu-Caputo, Nathalie Loux, Marion Andreoletti, Karen Westerman, Pascale Briand, Dominique Franco, Philippe Leboulch, Anne Weber

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.6field-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

21 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Redox-Dependent Modulation of Human Liver Progenitor Cell Line Fate.International journal of molecular sciences · 2023
    Article
  3. Article
  4. Article
  5. Review
  6. Immortalized common marmoset (Cell discovery · 2018
    Article
  7. Article
  8. Review
  9. Article
  10. Ontogenesis of hepatic and pancreatic stem cells.Stem cell reviews and reports · 2012
    Review
  11. Article
  12. Progress in stem cell-derived technologies for hepatocellular carcinoma.Stem cells and cloning : advances and applications · 2010
    Review
  13. Article
  14. Stem cells in the adult pancreas and liver.The Biochemical journal · 2007
    Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  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

10 authors at 1 institution in 1 country.

Jean-Etienne AllainEquipe Mixte Inserm 00-20, Laboratoire de Transfert de Gènes Dans le Foie: Applications Thérapeutiques, Hôpital Antoine-Béclère, 157 Rue de la Porte de Trivaux, 92141 Clamart, France.
Ibrahim Dagher
Dominique Mahieu-Caputo
Nathalie Loux
Marion Andreoletti
Karen Westerman
Pascale Briand
Dominique Franco
Philippe Leboulch
Anne Weber
Inserm · FR

Funding

STEM CELLS AND GENE THERAPY MODELSP01HL055435 · NHLBI · YESHIVA UNIVERSITY · PI NAGEL, RONALD L · 1995 to 2004
$11.0M
GENE THERAPY FOR ERYTHROPOIETIC PROTOPORPHYRIAR01DK056174 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI MATHEWS-ROTH, MICHELINE M · 1999 to 2002
$953k
NHLBI NIH HHS HL55435NHLBI NIH HHS P01 HL055435NIDDK NIH HHS DK56174NIDDK NIH HHS R01 DK056174
6 · The paper itself

Abstract

Liver regeneration after partial hepatectomy results primarily from the simple division of mature hepatocytes. However, during embryonic and fetal development or in circumstances under which postnatal hepatocytes are injured, organ regeneration is believed to occur from a compartment of epithelial liver stem or progenitor cells with biliary and hepatocytic bipotentiality. The ability to identify, isolate, and transplant epithelial liver stem cells from fetal liver would greatly facilitate the treatment of hepatic diseases currently requiring orthotopic liver transplantation. Here we report the identification and immortalization by retrovirus-mediated transfer of the simian virus 40 large T antigen gene of primate fetal epithelial liver cells with a dual hepatocytic biliary phenotype. These cells grow indefinitely in vitro and express the liver epithelial cell markers cytokeratins 8/18, the hepatocyte-specific markers albumin and alpha-fetoprotein, and the biliary-specific markers cytokeratins 7 and 19. Bipotentiality of gene expression was confirmed by clonal analysis initiated from single cells. Endogenous telomerase also is expressed constitutively. After orthotopic transplantation via the portal vein, approximately 50% of the injected cells integrated into the liver parenchyma of athymic mice without tumorigenicity. Three weeks after transplantation, cells having seeded in the liver parenchyma expressed both albumin and alpha-fetoprotein but had lost expression of cytokeratin 19. These results provide strong evidence for the existence of a bipotent epithelial liver stem cell in nonhuman primates. This unlimited source of donor cells also should enable the establishment of a model of allogenic liver cell transplantation in a large animal closely related to humans and shed light on important questions related to liver organogenesis and differentiation.

Indexed as

Albuminsalpha-FetoproteinsAnimalsBiomarkersCell DifferentiationCell DivisionCells, CulturedCell Transformation, NeoplasticCell TransplantationChimeraClone CellsEmbryonic and Fetal DevelopmentEpithelial CellsFetusGene Expression Regulation, DevelopmentalKeratinsAlbuminsalpha-FetoproteinsBiomarkersKeratinsTelomerase

Identifiers

PMID11904425
PMCPMC122576
OpenAlexW1991624884

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.