Evidence map›Paper›PMID 37653039›Full record

ArticleExperimental & molecular medicine2023

Scalable production of tissue-like vascularized liver organoids from human PSCs.

Sean P Harrison, Richard Siller, Yoshiaki Tanaka, Maria Eugenia Chollet, María Eugenia de la Morena-Barrio, Yangfei Xiang, Benjamin Patterson, Elisabeth Andersen, Carlos Bravo-Pérez, Henning Kempf and 26 more

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
17.7field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. [Organoid-based strategies and challenges in tissue regeneration].Zhonghua shao shang yu chuang mian xiu fu za zhi · 2026
    Pooled it
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Biobanked Liver Organoids: A Roadmap for Precision Hepatology.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
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  12. Review
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  14. Review
  15. Article
  16. Article
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  19. Haematologica · 2026
    Article
  20. Review

11 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

36 authors at 9 institutions in 8 countries.

Sean P Harrison *Hybrid Technology Hub-Centre of Excellence, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.ORCID 0000-0001-9399-9631
Richard Siller *Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Yoshiaki Tanaka *Department of Genetics, Yale Stem Cell Center, Child Study Center, Yale School of Medicine, New Haven, USA.ORCID 0000-0002-2078-9374
Maria Eugenia Chollet *Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
María Eugenia de la Morena-BarrioServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB, CIBERER, Murcia, Spain.
Yangfei XiangDepartment of Genetics, Yale Stem Cell Center, Child Study Center, Yale School of Medicine, New Haven, USA.ORCID 0000-0002-6256-6312
Benjamin PattersonDepartment of Genetics, Yale Stem Cell Center, Child Study Center, Yale School of Medicine, New Haven, USA.
Elisabeth AndersenResearch Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
Carlos Bravo-PérezServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB, CIBERER, Murcia, Spain.
Henning KempfDepartment: Leibniz Research Laboratories for Biotechnology and Artificial Organs (LEBAO), Hannover Medical School, Hannover, Germany.
Kathrine S ÅsrudNorwegian PSC Research Center, Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
Oleg LunovDepartment of Optical and Biophysical Systems, Institute of Physics of the Czech Academy of Sciences, Prague, Czech Republic.
Alexandr DejnekaDepartment of Optical and Biophysical Systems, Institute of Physics of the Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0002-5116-8781
Marie-Christine MowinckelResearch Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
Benedicte StavikResearch Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
Per Morten SandsetResearch Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
Espen MelumHybrid Technology Hub-Centre of Excellence, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Saphira BaumgartenHybrid Technology Hub-Centre of Excellence, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Flavio BonaniniMimetas, Leiden, The Netherlands.
Dorota KurekMimetas, Leiden, The Netherlands.
Santosh MathapatiDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Runar AlmaasDepartment of Pediatric Research, Oslo University Hospital, Oslo, Norway.
Kulbhushan SharmaDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Steven R WilsonHybrid Technology Hub-Centre of Excellence, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Frøydis S SkottvollHybrid Technology Hub-Centre of Excellence, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Ida C BogerDepartment of Chemistry, University of Oslo, P.O. Box 1033, Blindern, NO-0315, Oslo, Norway.
Inger Lise BogenDepartment of Forensic Sciences, Oslo University Hospital, Oslo, Norway.
Tuula A NymanDepartment of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Jun Jie WuDepartment of Engineering, Faculty of Science, Durham University, Durham, DH1 3LE, United Kingdom.
Ales BezroukDepartment of Medical Biophysics, Faculty of Medicine in Hradec Králové, Charles University, Hradec Králové, Czech Republic.
Dana CizkovaDepartment of Histology and Embryology, Faculty of Medicine in Hradec Králové, Charles University, Hradec Králové, Czech Republic.
Javier CorralServicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación, Universidad de Murcia, IMIB, CIBERER, Murcia, Spain.
Jaroslav MokryDepartment of Histology and Embryology, Faculty of Medicine in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID 0000-0001-5769-9973
Robert ZweigerdtDepartment: Leibniz Research Laboratories for Biotechnology and Artificial Organs (LEBAO), Hannover Medical School, Hannover, Germany.
In-Hyun ParkDepartment of Genetics, Yale Stem Cell Center, Child Study Center, Yale School of Medicine, New Haven, USA.ORCID 0000-0001-7748-1293
Gareth J SullivanHybrid Technology Hub-Centre of Excellence, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway. garethsully@hotmail.com.
Oslo University Hospital · NOUniversity of Oslo · NOYale Cancer Center · USCentro Regional de Hemodonación · ESCharles University · CZCzech Academy of Sciences · CZMedizinische Hochschule Hannover · DEMimetas (Netherlands) · NLDurham University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The lack of physiological parity between 2D cell culture and in vivo culture has led to the development of more organotypic models, such as organoids. Organoid models have been developed for a number of tissues, including the liver. Current organoid protocols are characterized by a reliance on extracellular matrices (ECMs), patterning in 2D culture, costly growth factors and a lack of cellular diversity, structure, and organization. Current hepatic organoid models are generally simplistic and composed of hepatocytes or cholangiocytes, rendering them less physiologically relevant compared to native tissue. We have developed an approach that does not require 2D patterning, is ECM independent, and employs small molecules to mimic embryonic liver development that produces large quantities of liver-like organoids. Using single-cell RNA sequencing and immunofluorescence, we demonstrate a liver-like cellular repertoire, a higher order cellular complexity, presenting with vascular luminal structures, and a population of resident macrophages: Kupffer cells. The organoids exhibit key liver functions, including drug metabolism, serum protein production, urea synthesis and coagulation factor production, with preserved post-translational modifications such as N-glycosylation and functionality. The organoids can be transplanted and maintained long term in mice producing human albumin. The organoids exhibit a complex cellular repertoire reflective of the organ and have de novo vascularization and liver-like function. These characteristics are a prerequisite for many applications from cellular therapy, tissue engineering, drug toxicity assessment, and disease modeling to basic developmental biology.

Indexed as

LiverOrganoidsAnimalsCells, CulturedHepatocytesHumansMiceTissue Engineering

Identifiers

PMID37653039
PMCPMC10545717
OpenAlexW4386318431

What Socratic 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 Socratic graph.