Evidence map›Paper›PMID 29844473›Full record

ArticleScientific reports2018

Expansion of human primary hepatocytes in vitro through their amplification as liver progenitors in a 3D organoid system.

Delphine Garnier, Ruoya Li, Frédéric Delbos, Angélique Fourrier, Camille Collet, Christiane Guguen-Guillouzo, Christophe Chesné, Tuan Huy Nguyen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
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  9. Liver organoid culture methods.Cell & bioscience · 2023
    Review
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  11. Review
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  16. Development ofFrontiers in immunology · 2022
    Article
  17. 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

8 authors at 3 institutions in 1 country.

Delphine GarnierINSERM, Université de Nantes, Centre de Recherche en Transplantation et Immunologie UMR 1064, Nantes, France. delphine.garnier@univ-nantes.fr.
Ruoya LiBiopredic International, Saint-Grégoire, France.
Frédéric DelbosINSERM, Université de Nantes, Centre de Recherche en Transplantation et Immunologie UMR 1064, Nantes, France.
Angélique FourrierINSERM, Université de Nantes, Centre de Recherche en Transplantation et Immunologie UMR 1064, Nantes, France.
Camille ColletINSERM, Université de Nantes, Centre de Recherche en Transplantation et Immunologie UMR 1064, Nantes, France.
Christiane Guguen-GuillouzoBiopredic International, Saint-Grégoire, France.
Christophe ChesnéBiopredic International, Saint-Grégoire, France.
Tuan Huy NguyenINSERM, Université de Nantes, Centre de Recherche en Transplantation et Immunologie UMR 1064, Nantes, France.
Inserm · FRBiopredic (France) · FRNantes Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite decades of investigation on the proliferation of adult human primary hepatocytes, their expansion in vitro still remains challenging. To later be able to consider hepatocytes as a cell therapy alternative or bridge to liver transplantation, dramatically impeded by a shortage in liver donors, the first step is having an almost unlimited source of these cells. The banking of transplantable hepatocytes also implies a protocol for their expansion that can be compatible with large-scale production. We show that adult human primary hepatocytes when grown in 3D organoids are easily amplified, providing a substantial source of functional hepatocytes ready for transplantation. Following their plating, differentiated human hepatocytes are amplified during a transient and reversible step as liver progenitors, and can subsequently be converted back to mature differentiated hepatocytes. The protocol we propose is not only compatible with automated and high-throughput cell culture systems, thanks to the expansion of hepatocytes in suspension, but also guarantees the generation of a high number of functional cells from the same patient sample, with a relatively easy set up.

Indexed as

AdultAgedCell DifferentiationCells, CulturedCollagenDrug CombinationsFemaleHepatocytesHumansLamininMaleOrganoidsProteoglycansStem CellsTissue EngineeringCollagenDrug CombinationsLamininmatrigelProteoglycans

Identifiers

PMID29844473
PMCPMC5974235
OpenAlexW2807297020

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.