Evidence map›Paper›PMID 31393263›Full record

ArticleeLife2019

Generation of human hepatic progenitor cells with regenerative and metabolic capacities from primary hepatocytes.

Takeshi Katsuda, Juntaro Matsuzaki, Tomoko Yamaguchi, Yasuhiro Yamada, Marta Prieto-Vila, Kazunori Hosaka, Atsuko Takeuchi, Yoshimasa Saito, Takahiro Ochiya

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 88 citations in OpenAlex.

  1. Review
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Bioengineered Bile Duct for Liver Regenerative Medicine and Bile Duct Reconstruction.JGH open : an open access journal of gastroenterology and hepatology · 2025
    Review
  10. Review
  11. Cell therapy for liver disorders: past, present and future.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Takeshi KatsudaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3960-033X
Juntaro MatsuzakiDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.ORCID http://orcid.org/0000-0002-3204-5049
Tomoko YamaguchiDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Yasuhiro YamadaDepartment of Clinical Pharmaceutics, Nihon Pharmaceutical University, Saitama, Japan.
Marta Prieto-VilaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Kazunori HosakaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Atsuko TakeuchiDivision of Analytical Laboratory, Kobe Pharmaceutical University, Kobe, Japan.
Yoshimasa SaitoDivision of Pharmacotherapeutics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
Takahiro OchiyaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0776-9918
Keio University · JPKobe Pharmaceutical University · JPNihon Pharmaceutical University · JPTokyo Medical University · JP

Funding

Japan Agency for Medical Research and Development 16fk0310512h0005Japan Agency for Medical Research and Development 17fk0310101h0001Japan Society for the Promotion of Science London 16K16643
6 · The paper itself

Abstract

Hepatocytes are regarded as the only effective cell source for cell transplantation to treat liver diseases; however, their availability is limited due to a donor shortage. Thus, a novel cell source must be developed. We recently reported that mature rodent hepatocytes can be reprogrammed into progenitor-like cells with a repopulative capacity using small molecule inhibitors. Here, we demonstrate that hepatic progenitor cells can be obtained from human infant hepatocytes using the same strategy. These cells, named human chemically induced liver progenitors (hCLiPs), had a significant repopulative capacity in injured mouse livers following transplantation. hCLiPs redifferentiated into mature hepatocytes in vitro upon treatment with hepatic maturation-inducing factors. These redifferentiated cells exhibited cytochrome P450 (CYP) enzymatic activities in response to CYP-inducing molecules and these activities were comparable with those in primary human hepatocytes. These findings will facilitate liver cell transplantation therapy and drug discovery studies.

Indexed as

AnimalsCell Culture TechniquesCell DifferentiationCell ProliferationCells, CulturedDisease Models, AnimalHepatocytesHumansInfantLiverRegenerationStem CellsStem Cell TransplantationTreatment Outcomecell biologycytochrome P450hepatocytehumanliver progenitor cellliver repopulationmouseregenerative medicinestem cellstransplantation

Identifiers

PMID31393263
PMCPMC6731094
OpenAlexW2967489505

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.