Evidence map›Paper›PMID 26592180›Full record

ArticleScientific reports2015

Engraftment of human induced pluripotent stem cell-derived hepatocytes in immunocompetent mice via 3D co-aggregation and encapsulation.

Wei Song, Yen-Chun Lu, Angela S Frankel, Duo An, Robert E Schwartz, Minglin Ma

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
3.9field-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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Lessons Learned from Liver-on-Chip Platform.Annals of biomedical engineering · 2025
    Review
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  5. Article
  6. Review
  7. Review
  8. Review
  9. A nucleosome switch primes Hepatitis B Virus infection.bioRxiv : the preprint server for biology · 2024
    Article
  10. Review
  11. Review
  12. Engineered organoids for biomedical applications.Advanced drug delivery reviews · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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 1 institution in 1 country.

Wei SongDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14850, USA.
Yen-Chun LuDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14850, USA.
Angela S FrankelDivision of Gastroenterology &Hepatology, Department of Medicine, Weill Medical College of Cornell University, New York, NY 10021, USA.
Duo AnDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14850, USA.
Robert E SchwartzDivision of Gastroenterology &Hepatology, Department of Medicine, Weill Medical College of Cornell University, New York, NY 10021, USA.
Minglin MaDepartment of Biological and Environmental Engineering, Cornell University, Ithaca, NY 14850, USA.
Cornell University · US

Funding

New Hepatocyte Model Systems to study Hepatitis B Virus InfectionK08DK101754 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI SCHWARTZ, ROBERT E · 2014 to 2018
$781k
Impact of species-specific host responses on restriction of hepatotropic virusesR21AI117213 · NIAID · PRINCETON UNIVERSITY · PI PLOSS, ALEXANDER, SCHWARTZ, ROBERT E · 2015 to 2016
$471k
NIAID NIH HHS R21 AI117213NIDDK NIH HHS 1K08DK101754NIDDK NIH HHS K08 DK101754
6 · The paper itself

Abstract

Cellular therapies for liver diseases and in vitro models for drug testing both require functional human hepatocytes (Hum-H), which have unfortunately been limited due to the paucity of donor liver tissues. Human pluripotent stem cells (hPSCs) represent a promising and potentially unlimited cell source to derive Hum-H. However, the hepatic functions of these hPSC-derived cells to date are not fully comparable to adult Hum-H and are more similar to fetal ones. In addition, it has been challenging to obtain functional hepatic engraftment of these cells with prior studies having been done in immunocompromised animals. In this report, we demonstrated successful engraftment of human induced pluripotent stem cell (iPSC)-derived hepatocyte-like cells (iPS-H) in immunocompetent mice by pre-engineering 3D cell co-aggregates with stromal cells (SCs) followed by encapsulation in recently developed biocompatible hydrogel capsules. Notably, upon transplantation, human albumin and α1-antitrypsin (A1AT) in mouse sera secreted by encapsulated iPS-H/SCs aggregates reached a level comparable to the primary Hum-H/SCs control. Further immunohistochemistry of human albumin in retrieved cell aggregates confirmed the survival and function of iPS-H. This proof-of-concept study provides a simple yet robust approach to improve the engraftment of iPS-H, and may be applicable to many stem cell-based therapies.

Indexed as

Graft SurvivalAlbuminsalpha 1-AntitrypsinAnimalsCell AggregationCell- and Tissue-Based TherapyCell DifferentiationCells, ImmobilizedCoculture TechniquesHepatocytesHumansHydrogelsImmunocompetenceInduced Pluripotent Stem CellsMiceMice, Inbred C57BLAlbuminsalpha 1-AntitrypsinHydrogels

Identifiers

PMID26592180
PMCPMC4655358
OpenAlexW2416653861

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.