Evidence map›Paper›PMID 23940571›Full record

ArticlePloS one2013

Gastrin: a distinct fate of neurogenin3 positive progenitor cells in the embryonic pancreas.

Yaron Suissa, Judith Magenheim, Miri Stolovich-Rain, Ayat Hija, Patrick Collombat, Ahmed Mansouri, Lori Sussel, Beatriz Sosa-Pineda, Kyle McCracken, James M Wells and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.9field-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

33 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  7. Review
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  14. Article
  15. Animal Models of Pancreas Development, Developmental Disorders, and Disease.Advances in experimental medicine and biology · 2020
    Review
  16. Article
  17. Review
  18. Modelling the endocrine pancreas in health and disease.Nature reviews. Endocrinology · 2019
    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

13 authors at 7 institutions in 5 countries.

Yaron SuissaEndocrinology and Metabolism Service, Department of Internal Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Judith Magenheim
Miri Stolovich-Rain
Ayat Hija
Patrick Collombat
Ahmed Mansouri
Lori Sussel
Beatriz Sosa-Pineda
Kyle McCracken
James M Wells
R Scott Heller
Yuval Dor
Benjamin Glaser
Cincinnati Children's Hospital Medical Center · USHadassah Medical Center · ILColumbia University · USInserm · FRMax Planck Institute for Biophysical Chemistry · DENovo Nordisk (Denmark) · DKSt. Jude Children's Research Hospital · US

Funding

RESEARCH TRAININGP30DK026687 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI Anthony W Ferrante, DYMPNA GALLAGHER · 1986 to 2026
$33.0M
Regulation of Pancreatic Islet Cell FateR01DK082590 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LORI SUSSEL · 2009 to 2026
$7.3M
Defining the roles of Nkx2.2 and NeuroD in regulating islet cell fateU01DK072504 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI SUSSEL, LORI · 2005 to 2010
$3.2M
NIDDK NIH HHS U01 DK072504
6 · The paper itself

Abstract

Neurogenin3(+) (Ngn3(+)) progenitor cells in the developing pancreas give rise to five endocrine cell types secreting insulin, glucagon, somatostatin, pancreatic polypeptide and ghrelin. Gastrin is a hormone produced primarily by G-cells in the stomach, where it functions to stimulate acid secretion by gastric parietal cells. Gastrin is expressed in the embryonic pancreas and is common in islet cell tumors, but the lineage and regulators of pancreatic gastrin(+) cells are not known. We report that gastrin is abundantly expressed in the embryonic pancreas and disappears soon after birth. Some gastrin(+) cells in the developing pancreas co-express glucagon, ghrelin or pancreatic polypeptide, but many gastrin(+) cells do not express any other islet hormone. Pancreatic gastrin(+) cells express the transcription factors Nkx6.1, Nkx2.2 and low levels of Pdx1, and derive from Ngn3(+) endocrine progenitor cells as shown by genetic lineage tracing. Using mice deficient for key transcription factors we show that gastrin expression depends on Ngn3, Nkx2.2, NeuroD1 and Arx, but not Pax4 or Pax6. Finally, gastrin expression is induced upon differentiation of human embryonic stem cells to pancreatic endocrine cells expressing insulin. Thus, gastrin(+) cells are a distinct endocrine cell type in the pancreas and an alternative fate of Ngn3+ cells.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsFlow CytometryGastrinsHomeobox Protein Nkx-2.2Homeodomain ProteinsMiceMice, KnockoutNerve Tissue ProteinsNuclear ProteinsPancreasReverse Transcriptase Polymerase Chain ReactionStem CellsTranscription FactorsZebrafish ProteinsBasic Helix-Loop-Helix ProteinsGastrinsHomeobox Protein Nkx-2.2Homeodomain ProteinsNerve Tissue ProteinsNeurog3 protein, mouseNeurogenic differentiation factor 1nkx2.2b protein, zebrafishNKX2-2 protein, humanNkx2-2 protein, mouseNkx6-1 protein, mouseNuclear ProteinsTranscription FactorsZebrafish Proteins

Identifiers

PMID23940571
PMCPMC3734289
OpenAlexW1977399878

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.