Evidence map›Paper›PMID 18410733›Full record

ArticleDevelopmental cell2008

Intra-endodermal interactions are required for pancreatic beta cell induction.

Won-Suk Chung, Didier Y R Stainier

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 103 citations in OpenAlex.

  1. Transcriptional divergence of the zebrafishbioRxiv : the preprint server for biology · 2026
    Article
  2. Met regulates endoderm migration in zebrafish.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Pancreatic organogenesis mapped through space and time.Experimental & molecular medicine · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. A single-cell-resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Review
  19. Article
  20. Article

5 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Won-Suk ChungDepartment of Biochemistry and Biophysics, and the Diabetes Center, University of California, San Francisco, 1550 4th Street, San Francisco, CA 94158, USA.
Didier Y R Stainier
University of California, San Francisco · US

Funding

Molecular Control of Pancreatic Islet DevelopmentU19DK061245 · NIDDK · UNIVERSITY OF CHICAGO · PI GERMAN, MICHAEL S · 2001 to 2005
$5.9M
MOLECULAR GENETICS OF PANCREAS DEVELOPMENTR01DK075032 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STAINIER, DIDIER Y · 2007 to 2011
$1.5M
NIDDK NIH HHS DK61245NIDDK NIH HHS DK75032NIDDK NIH HHS R01 DK075032NIDDK NIH HHS U19 DK061245
6 · The paper itself

Abstract

The cellular origin of signals that regulate pancreatic beta cell induction is not clearly defined. Here, we investigate the seeming paradox that Hedgehog/Smoothened signaling functions during gastrulation to promote pancreatic beta cell development in zebrafish, yet has an inhibitory role during later stages of pancreas development in amniotes. Our cell transplantation experiments reveal that in zebrafish, Smoothened function is not required in beta cell precursors. At early somitogenesis stages, when the zebrafish endoderm first forms a sheet, pancreatic beta cell precursors lie closest to the midline; however, the requirement for Smoothened lies in their lateral neighbors, which ultimately give rise to the exocrine pancreas and intestine. Thus, pancreatic beta cell induction requires Smoothened function cell-nonautonomously during gastrulation, to allow subsequent intra-endodermal interactions. These results clarify the function of Hedgehog signaling in pancreas development, identify an unexpected cellular source of factors that regulate beta cell specification, and uncover complex patterning and signaling interactions within the endoderm.

Indexed as

ZebrafishAnimalsAnimals, Genetically ModifiedCell DifferentiationCell LineageCell TransplantationEmbryonic InductionEndodermHedgehog ProteinsInsulin-Secreting CellsMesodermReceptors, G-Protein-CoupledRecombinant Fusion ProteinsSignal TransductionSmoothened ReceptorTransgenesHedgehog ProteinsReceptors, G-Protein-CoupledRecombinant Fusion ProteinsSmoothened Receptorsmo protein, zebrafishZebrafish Proteins

Identifiers

PMID18410733
PMCPMC2396532
OpenAlexW2059813768

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.