Evidence map›Paper›PMID 20413689›Full record

ArticleThe American journal of pathology2010

The role of the Wnt family of secreted proteins in rat oval "stem" cell-based liver regeneration: Wnt1 drives differentiation.

Jennifer M Williams, Seh-Hoon Oh, Marda Jorgensen, Nicole Steiger, Houda Darwiche, Thomas Shupe, Bryon E Petersen

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Role of Immune Cells in Biliary Repair.Frontiers in immunology · 2022
    Review
  5. Article
  6. Article
  7. Wnt-β-catenin signalling in liver development, health and disease.Nature reviews. Gastroenterology & hepatology · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Targeting the Wnt pathways for therapies.Molecular and cellular therapies · 2014
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Jennifer M WilliamsUniversity of Florida College of Medicine, Department of Pathology, PO Box 100275, 1600 SW Archer Rd., Gainesville, FL 32610, USA.
Seh-Hoon Oh
Marda Jorgensen
Nicole Steiger
Houda Darwiche
Thomas Shupe
Bryon E Petersen
University of Florida · USFlorida College · US

Funding

Mechanisms of Oval Cell Activation and DifferentiationR01DK058614 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2001 to 2014
$3.6M
Stem Cells in Liver Regeneration: Fusion or PlasticityR01DK065096 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2005 to 2013
$2.7M
Mechanisms of Oval Cell Activation and DifferentiationR56DK058614 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2010 to 2010
$451k
BONE MARROW AS A SOURCE FOR PANCREATIC STEM CELLSR21DK060015 · NIDDK · UNIVERSITY OF FLORIDA · PI PETERSEN, BRYON E · 2001 to 2002
$290k
NIDDK NIH HHS DK58614NIDDK NIH HHS DK60015NIDDK NIH HHS R01 DK058614NIDDK NIH HHS R01 DK065096NIDDK NIH HHS R56 DK058614
6 · The paper itself

Abstract

To date the molecular signals regulating activation, proliferation, and differentiation of hepatic oval cells are not fully understood. The Wnt family is essential in hepatic embryogenesis and implicated in hepatic carcinogenesis. This study elucidates novel findings implicating Wnt1 in directing oval cell differentiation during the rat 2-acetylaminofluorene (2AAF) and 2/3 partial hepatectomy (PHx) liver regeneration model. Proteins of Wnt family members were predominantly localized in pericentral hepatocytes during liver injury, oval cell activation, and hepatocyte regeneration. In addition, Wnt message increased coinciding with the rise in oval cell number, whereas protein levels peaked immediately after the height of oval cell proliferation. Immunohistochemical analysis demonstrated nuclear translocation of beta-catenin within oval cells throughout the 2AAF/PHx protocol. Furthermore, RNA interference was used in vivo to confirm the physiological requirement of Wnt1 during the oval cell induction. Ultimately, inhibition of Wnt1 resulted in failure of oval cells to differentiate into hepatocytes and alternatively induced atypical ductular hyperplasia. Taken together, these data indicate that in vivo exposure to Wnt1 shRNA inhibited rat oval cell liver regeneration. In the absence of Wnt1 signaling, oval cells failed to differentiate into hepatocytes and underwent atypical ductular hyperplasia, exhibiting epithelial metaplasia and mucin production. Furthermore, changes in Wnt1 levels are required for the efficient regeneration of the liver by oval cells during massive hepatic injury.

Indexed as

2-Acetylaminofluorenealpha-FetoproteinsAnimalsAntigens, Differentiationbeta CateninCarcinogensCell DifferentiationFrizzled ReceptorsHepatectomyLiverLiver RegenerationMaleOrgan SizeRatsRats, Inbred F344Receptors, G-Protein-Coupled2-Acetylaminofluorenealpha-FetoproteinsAntigens, Differentiationbeta CateninCarcinogensCtnnb1 protein, ratFrizzled ReceptorsFzd1 protein, ratoval cell marker OV-6Receptors, G-Protein-CoupledReceptors, NeurotransmitterWnt1 ProteinWnt1 protein, rat

Identifiers

PMID20413689
PMCPMC2877835
OpenAlexW1544757832

What OpenQuestion holds

Textmetadata
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.