Evidence map›Paper›PMID 25773748›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2015

Fate mapping of ptf1a-expressing cells during pancreatic organogenesis and regeneration in zebrafish.

Yue J Wang, Joon T Park, Michael J Parsons, Steven D Leach

Open access · bronzeAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

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  14. Zebrafish model ofAnimal cells and systems · 2018
    Article
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  17. Disease models & mechanisms · 2017
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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

4 authors at 2 institutions in 1 country.

Yue J WangThe McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Joon T ParkThe Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Michael J ParsonsThe McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Steven D LeachThe McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

SURGICAL STUDIES OF PANCREATIC STEM CELLSR01DK056211 · NIDDK · VANDERBILT UNIVERSITY · PI LEACH, STEVEN D · 1999 to 2014
$4.9M
Identifying the Progenitors Responsible for Beta Cell Regeneration in ZebrafishR01DK080730 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI PARSONS, MICHAEL J · 2008 to 2021
$4.5M
Regulation of Exocrine Pancreatic Progenitors by Ptf1a-p48R01DK061215 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI LEACH, STEVEN D · 2002 to 2012
$3.3M
Defining the Pancreatic Progenitor Mesenchymal NicheR01DK097087 · NIDDK · SLOAN-KETTERING INST CAN RESEARCH · PI JENSEN, JAN, LEACH, STEVEN D · 2013 to 2016
$1.7M
NIDDK NIH HHS DK056211NIDDK NIH HHS DK080730NIDDK NIH HHS DK097087NIDDK NIH HHS R01 DK056211NIDDK NIH HHS R01 DK061215NIDDK NIH HHS R01 DK080730NIDDK NIH HHS R01 DK097087
6 · The paper itself

Abstract

backgroundPancreas development in zebrafish shares many features with mammals, including the participation of epithelial progenitor cells expressing pancreas transcription factor 1a (ptf1a). However, to date it has remained unclear whether, as in mammals, ptf1a-expressing zebrafish pancreatic progenitors are able to contribute to multiple exocrine and endocrine lineages. To delineate the lineage potential of ptf1a-expressing cells, we generated ptf1a:creER(T2) transgenic fish and performed genetic-inducible lineage tracing in developmental, regenerating, and ptf1a-deficient zebrafish pancreas.

resultsIn addition to their contribution to the acinar cell lineage, ptf1a-expressing cells give rise to both pancreatic Notch-responsive-cells (PNCs) as well as small numbers of endocrine cells during pancreatic development. In fish with ptf1a haploinsufficiency, a higher proportion of ptf1a lineage-labeled cells are traced into the PNC and endocrine compartments. Further reduction of ptf1a gene dosage converts pancreatic progenitor cells to gall bladder and other non-pancreatic cell fates.

conclusionsOur results confirm the presence of multipotent ptf1a-expressing progenitor cells in developing zebrafish pancreas, with reduced ptf1a dosage promoting greater contributions towards non-acinar lineages. As in mammals, loss of ptf1a results in conversion of nascent pancreatic progenitor cells to non-pancreatic cell fates, underscoring the central role of ptf1a in foregut tissue specification.

Indexed as

Acinar CellsAnimalsAnimals, Genetically ModifiedCell LineageChromosomes, Artificial, BacterialGallbladderGene DosageGenotypeIslets of LangerhansOrgan SpecificityPancreasPancreas, ExocrineReceptors, NotchRecombination, GeneticRegenerationStem CellsReceptors, Notchtranscription factor PTF1Transcription Factorsendocrinelineage tracingpancreaspancreatic Notch-responsive cellsptf1a

Identifiers

PMID25773748
PMCPMC4838417
OpenAlexW1930878639

What OpenQuestion holds

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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.