Evidence map›Paper›PMID 30375438›Full record

ArticleScientific reports2018

Mesenchymal stromal cells prevent progression of liver fibrosis in a novel zebrafish embryo model.

Danny van der Helm, Arwin Groenewoud, Eveline S M de Jonge-Muller, Marieke C Barnhoorn, Mark J A Schoonderwoerd, Minneke J Coenraad, Lukas J A C Hawinkels, B Ewa Snaar-Jagalska, Bart van Hoek, Hein W Verspaget

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Using different zebrafish models to explore liver regeneration.Frontiers in cell and developmental biology · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Using Zebrafish as a Disease Model to Study Fibrotic Disease.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. 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

10 authors at 2 institutions in 1 country.

Danny van der HelmDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Arwin GroenewoudDepartment of Animal Science and Health, Leiden University, Leiden, The Netherlands.
Eveline S M de Jonge-MullerDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Marieke C BarnhoornDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Mark J A SchoonderwoerdDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Minneke J CoenraadDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Lukas J A C HawinkelsDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
B Ewa Snaar-JagalskaDepartment of Animal Science and Health, Leiden University, Leiden, The Netherlands.
Bart van HoekDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Hein W VerspagetDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands. H.W.Verspaget@lumc.nl.
Leiden University Medical Center · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic liver damage leads to the onset of fibrogenesis. Rodent models for liver fibrosis have been widely used, but are less suitable for screening purposes. Therefore the aim of our study was to design a novel model for liver fibrosis in zebrafish embryos, suitable for high throughput screening. Furthermore, we evaluated the efficacy of mesenchymal stromal cells (MSCs) to inhibit the fibrotic process and thereby the applicability of this model to evaluate therapeutic responses. Zebrafish embryos were exposed to TAA or CCL4 and mRNA levels of fibrosis-related genes (Collagen-1α1, Hand-2, and Acta-2) and tissue damage-related genes (TGF-β and SDF-1a, SDF-1b) were determined, while Sirius-red staining was used to estimate collagen deposition. Three days after start of TAA exposure, MSCs were injected after which the fibrotic response was determined. In contrast to CCL4, TAA resulted in an upregulation of the fibrosis-related genes, increased extracellular matrix deposition and decreased liver sizes suggesting the onset of fibrosis. The applicability of this model to evaluate therapeutic responses was shown by local treatment with MSCs which resulted in decreased expression of the fibrosis-related RNA markers. In conclusion, TAA induces liver fibrosis in zebrafish embryos, thereby providing a promising model for future mechanistic and therapeutic studies.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsBiomarkersChemokine CCL4Disease Models, AnimalDisease ProgressionEmbryo, NonmammalianFibroblastsGene ExpressionLiver CirrhosisMesenchymal Stem CellsThioacetamideZebrafishBiomarkersChemokine CCL4Thioacetamide

Identifiers

PMID30375438
PMCPMC6207680
OpenAlexW2898351901

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.