Evidence map›Paper›PMID 32108026›Full record

ArticleDevelopment (Cambridge, England)2020

Molecular and genetic regulation of pig pancreatic islet cell development.

Seokho Kim, Robert L Whitener, Heshan Peiris, Xueying Gu, Charles A Chang, Jonathan Y Lam, Joan Camunas-Soler, Insung Park, Romina J Bevacqua, Krissie Tellez and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Functional Inactivation ofInternational journal of molecular sciences · 2026
    Article
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  15. Article
  16. Frontiers in endocrinology · 2022
    Article
  17. Sequential in vivo labeling of insulin secretory granule pools inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  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

15 authors at 5 institutions in 1 country.

Seokho KimDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-9245-3776
Robert L WhitenerDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-0931-3586
Heshan PeirisDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Xueying GuDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Charles A ChangDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jonathan Y LamDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Joan Camunas-SolerDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Insung ParkDepartment of Animal Science, University of California Davis, Davis, CA 95616, USA.
Romina J BevacquaDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Krissie TellezDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Stephen R QuakeDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Jonathan R T LakeyDepartment of Surgery, University of California at Irvine, Irvine, CA 92868, USA.
Rita BottinoInstitute of Cellular Therapeutics, Allegheny Health Network, Pittsburgh, PA 15212, USA.
Pablo J RossDepartment of Animal Science, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0002-3972-3754
Seung K KimDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA seungkim@stanford.edu.ORCID 0000-0001-6135-7810
Stanford University · USUniversity of California, Davis · USAllegheny Health Network · USChan Zuckerberg Initiative (United States) · USUniversity of California, Irvine · US

Funding

Stanford Center for Clinical & Translational Education and Research (Spectrum)UL1TR003142 · NCATS · STANFORD UNIVERSITY · PI O'HARA, RUTH M · 2019 to 2023
$45.0M
Spectrum Stanford Center for clinical and Translational Research and EducationUL1TR001085 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$37.1M
Stanford Islet Research CoreP30DK116074 · NIDDK · STANFORD UNIVERSITY · PI Seung K Kim · 2017 to 2026
$19.5M
Diabetes, Endocrinology and Metabolism Training GrantT32DK007217 · NIDDK · STANFORD UNIVERSITY · PI Justin Pierce Annes, David Matthew Maahs · 1987 to 2026
$7.2M
NCATS NIH HHS UL1 TR001085NCATS NIH HHS UL1 TR003142NIDDK NIH HHS P30 DK116074NIDDK NIH HHS T32 DK007217
6 · The paper itself

Abstract

Reliance on rodents for understanding pancreatic genetics, development and islet function could limit progress in developing interventions for human diseases such as diabetes mellitus. Similarities of pancreas morphology and function suggest that porcine and human pancreas developmental biology may have useful homologies. However, little is known about pig pancreas development. To fill this knowledge gap, we investigated fetal and neonatal pig pancreas at multiple, crucial developmental stages using modern experimental approaches. Purification of islet β-, α- and δ-cells followed by transcriptome analysis (RNA-seq) and immunohistology identified cell- and stage-specific regulation, and revealed that pig and human islet cells share characteristic features that are not observed in mice. Morphometric analysis also revealed endocrine cell allocation and architectural similarities between pig and human islets. Our analysis unveiled scores of signaling pathways linked to native islet β-cell functional maturation, including evidence of fetal α-cell GLP-1 production and signaling to β-cells. Thus, the findings and resources detailed here show how pig pancreatic islet studies complement other systems for understanding the developmental programs that generate functional islet cells, and that are relevant to human pancreatic diseases.

Indexed as

SwineAnimalsAnimals, NewbornCell DifferentiationCells, CulturedEmbryo, MammalianFemaleFetusGene Expression ProfilingGene Expression Regulation, DevelopmentalGlucagon-Secreting CellsHumansInsulin-Secreting CellsIslets of LangerhansMiceOrganogenesisTranscription FactorsDiabetes mellitusMetabolismOrganogenesisPancreasPigα-Cellβ-Cellδ-cell

Identifiers

PMID32108026
PMCPMC7132804
OpenAlexW3007176590

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.