Evidence map›Paper›PMID 23720049›Full record

ArticleDevelopment (Cambridge, England)2013

Specification of hepatopancreas progenitors in zebrafish by hnf1ba and wnt2bb.

Joseph J Lancman, Natasha Zvenigorodsky, Keith P Gates, Danhua Zhang, Keely Solomon, Rohan K Humphrey, Taiyi Kuo, Linda Setiawan, Heather Verkade, Young-In Chi and 4 more

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Regenerative failure of intrahepatic biliary cells in Alagille syndrome rescued by elevated Jagged/Notch/Sox9 signaling.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Zebrafish as a Model for Obesity and Diabetes.Frontiers in cell and developmental biology · 2018
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. 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

14 authors at 3 institutions in 2 countries.

Joseph J LancmanSanford Children's Health Research Center, Programs in Genetic Disease, Development and Aging, and Stem Cell and Regenerative Biology, Graduate School of Biomedical Sciences, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.
Natasha Zvenigorodsky
Keith P Gates
Danhua Zhang
Keely Solomon
Rohan K Humphrey
Taiyi Kuo
Linda Setiawan
Heather Verkade
Young-In Chi
Ulupi S Jhala
Christopher V E Wright
Didier Y R Stainier
P Duc Si Dong
Vanderbilt University · USMonash University · AUUniversity of Minnesota · US

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Molecular Control of Pancreatic Islet DevelopmentU19DK061245 · NIDDK · UNIVERSITY OF CHICAGO · PI GERMAN, MICHAEL S · 2001 to 2005
$5.9M
Architecture and communication controlling the efficient generation of beta cellsU01DK089570 · NIDDK · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 2010 to 2014
$5.5M
Unlocking Regenerative Potential through in Vivo Genetic ReprogrammingDP2DK098092 · NIDDK · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI DONG, P. DUC SI · 2012 to 2012
$2.9M
MOLECULAR GENETICS OF PANCREAS DEVELOPMENTR01DK075032 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STAINIER, DIDIER Y · 2007 to 2011
$1.5M
NIDDK NIH HHS 1DP2DK098092NIDDK NIH HHS DK61245NIDDK NIH HHS DK75032NIDDK NIH HHS DP2 DK098092NIDDK NIH HHS P30 DK026743NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK075032NIDDK NIH HHS U01 DK089570NIDDK NIH HHS U19 DK061245
6 · The paper itself

Abstract

Although the liver and ventral pancreas are thought to arise from a common multipotent progenitor pool, it is unclear whether these progenitors of the hepatopancreas system are specified by a common genetic mechanism. Efforts to determine the role of Hnf1b and Wnt signaling in this crucial process have been confounded by a combination of factors, including a narrow time frame for hepatopancreas specification, functional redundancy among Wnt ligands, and pleiotropic defects caused by either severe loss of Wnt signaling or Hnf1b function. Using a novel hypomorphic hnf1ba zebrafish mutant that exhibits pancreas hypoplasia, as observed in HNF1B monogenic diabetes, we show that hnf1ba plays essential roles in regulating β-cell number and pancreas specification, distinct from its function in regulating pancreas size and liver specification, respectively. By combining Hnf1ba partial loss of function with conditional loss of Wnt signaling, we uncover a crucial developmental window when these pathways synergize to specify the entire ventrally derived hepatopancreas progenitor population. Furthermore, our in vivo genetic studies demonstrate that hnf1ba generates a permissive domain for Wnt signaling activity in the foregut endoderm. Collectively, our findings provide a new model for HNF1B function, yield insight into pancreas and β-cell development, and suggest a new mechanism for hepatopancreatic specification.

Indexed as

AnimalsAnimals, Genetically ModifiedCell DifferentiationHepatocyte Nuclear Factor 1-betaHepatopancreasSignal TransductionStem CellsWnt ProteinsZebrafishZebrafish ProteinsHepatocyte Nuclear Factor 1-betahnf1ba protein, zebrafishwnt2ba protein, zebrafishWnt ProteinsZebrafish ProteinsDiabetesHnf1bLiverMODYPancreasWnt

Identifiers

PMID23720049
PMCPMC3678338
OpenAlexW2101674354

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.