Evidence map›Paper›PMID 19403659›Full record

ArticleDevelopment (Cambridge, England)2009

The tetraspanin Tm4sf3 is localized to the ventral pancreas and regulates fusion of the dorsal and ventral pancreatic buds.

Zeina Jarikji, Lori Dawn Horb, Farhana Shariff, Craig A Mandato, Ken W Y Cho, Marko E Horb

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Tetraspanins Function as Regulators of Cellular Signaling.Frontiers in cell and developmental biology · 2017
    Review
  7. Article
  8. Review
  9. Xenopus as a Model for GI/Pancreas Disease.Current pathobiology reports · 2015
    Article
  10. Article
  11. Microarray analysis of Xenopus endoderm expressing Ptf1a.Genesis (New York, N.Y. : 2000) · 2012
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. From genetic association to molecular mechanism.Current diabetes reports · 2010
    Review
  18. Article
  19. Review
  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

6 authors at 4 institutions in 2 countries.

Zeina JarikjiLaboratory of Molecular Organogenesis, Institut de Recherches Cliniques de Montréal, Montreal, QC H2W 1R7, Canada.
Lori Dawn Horb
Farhana Shariff
Craig A Mandato
Ken W Y Cho
Marko E Horb
Centre Hospitalier de l’Université de Montréal · CAMcGill University · CAOrganogenesis (United States) · USUniversity of California, Irvine · US

Funding

Transcriptional Regulatory Networks Controlling Xenopus Pancreas DevelopmentR01DK077197 · NIDDK · MARINE BIOLOGICAL LABORATORY · PI HORB, MARKO E · 2007 to 2011
$1.1M
Regulation of call adhesion in XenopusR01GM075018 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CHO, KEN W.Y. · 2005 to 2009
$1.0M
NIDDK NIH HHS DK077197NIDDK NIH HHS R01 DK077197NIGMS NIH HHS GM075018
6 · The paper itself

Abstract

During embryogenesis, the pancreas develops from separate dorsal and ventral buds, which fuse to form the mature pancreas. Little is known about the functional differences between these two buds or the relative contribution of cells derived from each region to the pancreas after fusion. To follow the fate of dorsal or ventral bud derived cells in the pancreas after fusion, we produced chimeric Elas-GFP transgenic/wild-type embryos in which either dorsal or ventral pancreatic bud cells expressed GFP. We found that ventral pancreatic cells migrate extensively into the dorsal pancreas after fusion, whereas the converse does not occur. Moreover, we found that annular pancreatic tissue is composed exclusively of ventral pancreas-derived cells. To identify ventral pancreas-specific genes that may play a role in pancreatic bud fusion, we isolated individual dorsal and ventral pancreatic buds, prior to fusion, from NF38/39 Xenopus laevis tadpoles and compared their gene expression profiles (NF refers to the specific stage of Xenopus development). As a result of this screen, we have identified several new ventral pancreas-specific genes, all of which are expressed in the same location within the ventral pancreas at the junction where the two ventral pancreatic buds fuse. Morpholino-mediated knockdown of one of these ventral-specific genes, transmembrane 4 superfamily member 3 (tm4sf3), inhibited dorsal-ventral pancreatic bud fusion, as well as acinar cell differentiation. Conversely, overexpression of tm4sf3 promoted development of annular pancreas. Our results are the first to define molecular and behavioral differences between the dorsal and ventral pancreas, and suggest an unexpected role for the ventral pancreas in pancreatic bud fusion.

Indexed as

AnimalsAnimals, Genetically ModifiedBody PatterningEmbryo, NonmammalianFemaleGene Expression Regulation, DevelopmentalGene Knockdown TechniquesMaleMembrane GlycoproteinsMembrane ProteinsOligonucleotide Array Sequence AnalysisPancreasXenopusXenopus ProteinsMembrane GlycoproteinsMembrane ProteinsTSPAN8 protein, XenopusXenopus Proteins

Identifiers

PMID19403659
PMCPMC2680106
OpenAlexW1993384114

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.