Evidence map›Paper›PMID 25133500›Full record

ArticlePloS one2014

High throughput micro-well generation of hepatocyte micro-aggregates for tissue engineering.

Elien Gevaert, Laurent Dollé, Thomas Billiet, Peter Dubruel, Leo van Grunsven, Aart van Apeldoorn, Ria Cornelissen

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2014. 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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Review
  2. Frontiers in pharmacology · 2025
    Review
  3. Article
  4. Article
  5. The 3Rs in Experimental Liver Disease.Animals : an open access journal from MDPI · 2023
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. The Self-Assembling Process and Applications in Tissue Engineering.Cold Spring Harbor perspectives in medicine · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Cell sources for in vitro human liver cell culture models.Experimental biology and medicine (Maywood, N.J.) · 2016
    Review
  20. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors.

Elien GevaertTissue Engineering Group, Ghent University, Ghent, Belgium.
Laurent DolléLiver cell biology laboratory, Vrije Universiteit Brussels (VUB), Brussels, Belgium.
Thomas BillietPolymer Chemistry and Biomaterials Research Group, Ghent University, Ghent, Belgium.
Peter DubruelPolymer Chemistry and Biomaterials Research Group, Ghent University, Ghent, Belgium.
Leo van GrunsvenLiver cell biology laboratory, Vrije Universiteit Brussels (VUB), Brussels, Belgium.
Aart van ApeldoornDepartment of Developmental Bioengineering, University of Twente, Enschede, the Netherlands.
Ria CornelissenTissue Engineering Group, Ghent University, Ghent, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main challenge in hepatic tissue engineering is the fast dedifferentiation of primary hepatocytes in vitro. One successful approach to maintain hepatocyte phenotype on the longer term is the cultivation of cells as aggregates. This paper demonstrates the use of an agarose micro-well chip for the high throughput generation of hepatocyte aggregates, uniform in size. In our study we observed that aggregation of hepatocytes had a beneficial effect on the expression of certain hepatocyte specific markers. Moreover we observed that the beneficial effect was dependent on the aggregate dimensions, indicating that aggregate parameters should be carefully considered. In a second part of the study, the selected aggregates were immobilized by encapsulation in methacrylamide-modified gelatin. Phenotype evaluations revealed that a stable hepatocyte phenotype could be maintained during 21 days when encapsulated in the hydrogel. In conclusion we have demonstrated the beneficial use of micro-well chips for hepatocyte aggregation and the size-dependent effects on hepatocyte phenotype. We also pointed out that methacrylamide-modified gelatin is suitable for the encapsulation of these aggregates.

Indexed as

Cell Culture TechniquesAnimalsCells, CulturedCell SurvivalHepatocytesHep G2 CellsHumansHydrogel, Polyethylene Glycol DimethacrylateLiverMiceReal-Time Polymerase Chain ReactionTissue EngineeringHydrogel, Polyethylene Glycol Dimethacrylate

Identifiers

PMID25133500
PMCPMC4136852

What OpenQuestion holds

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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.