Evidence map›Paper›PMID 33542251›Full record

ArticleScientific reports2021

Response differences of HepG2 and Primary Mouse Hepatocytes to morphological changes in electrospun PCL scaffolds.

Thomas S R Bate, Victoria L Gadd, Stuart J Forbes, Anthony Callanan

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Rat liver ECM incorporated into electrospun polycaprolactone scaffolds as a platform for hepatocyte culture.Journal of biomedical materials research. Part B, Applied biomaterials · 2022
    Article
  8. Evolution of Electrospinning in Liver Tissue Engineering.Biomimetics (Basel, Switzerland) · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Article
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

4 authors.

Thomas S R BateInstitute for Bioengineering, School of Engineering, University of Edinburgh, Edinburgh, UK.
Victoria L GaddScottish Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Stuart J ForbesScottish Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Anthony CallananInstitute for Bioengineering, School of Engineering, University of Edinburgh, Edinburgh, UK. Anthony.Callanan@ed.ac.uk.

Funding

Medical Research Council MR/K017047/1Medical Research Council MR/L012766/1Medical Research Council MR/L022974/1Medical Research Council MR/R015635/1UK Regenerative Medicine Platform MR/R015635/1
6 · The paper itself

Abstract

Liver disease cases are rapidly expanding across the globe and the only effective cure for end-stage disease is a transplant. Transplant procedures are costly and current supply of donor livers does not satisfy demand. Potential drug treatments and regenerative therapies that are being developed to tackle these pressing issues require effective in-vitro culture platforms. Electrospun scaffolds provide bio-mimetic structures upon which cells are cultured to regulate function in-vitro. This study aims to shed light on the effects of electrospun PCL morphology on the culture of an immortalised hepatic cell line and mouse primary hepatocytes. Each cell type was cultured on large 4-5 µm fibres and small 1-2 µm fibres with random, aligned and highly porous cryogenically spun configurations. Cell attachment, proliferation, morphology and functional protein and gene expression was analysed. Results show that fibre morphology has a measurable influence on cellular morphology and function, with the alteration of key functional markers such as CYP1A2 expression.

Indexed as

AnimalsBiomimeticsCell ProliferationCytochrome P-450 CYP1A2Gene Expression RegulationHepatocytesHep G2 CellsHumansLiverLiver DiseasesMiceTissue EngineeringTissue ScaffoldsCytochrome P-450 CYP1A2

Identifiers

PMID33542251
PMCPMC7862353

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Registered trials

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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.