Evidence map›Paper›PMID 30361701›Full record

ArticleNature cell biology2018

Pancreatic islet-autonomous insulin and smoothened-mediated signalling modulate identity changes of glucagon

Valentina Cigliola, Luiza Ghila, Fabrizio Thorel, Léon van Gurp, Delphine Baronnier, Daniel Oropeza, Simone Gupta, Takeshi Miyatsuka, Hideaki Kaneto, Mark A Magnuson and 7 more

Abstract read
In one paragraph

Article in Nature cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
7.8field-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

41 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
  7. Hallmarks of regeneration.Cell stem cell · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Pancreatic δ Cells: An Overlooked Cell in Focus.Advances in anatomy, embryology, and cell biology · 2024
    Review
  14. Article
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  16. Article
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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

17 authors at 6 institutions in 4 countries.

Valentina CigliolaDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Luiza GhilaDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID http://orcid.org/0000-0001-7173-6312
Fabrizio ThorelDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Léon van GurpDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Delphine BaronnierDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Daniel OropezaDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Simone GuptaLilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN, USA.
Takeshi MiyatsukaDepartment of Metabolism and Endocrinology, Graduate School of Medicine , Juntendo University , Tokyo, Japan.
Hideaki KanetoDepartment of Metabolic Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.
Mark A MagnusonDepartments of Molecular Physiology and Biophysics, Center for Stem Cell Biology, Vanderbilt University, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-8824-6499
Anna B OsipovichDepartments of Molecular Physiology and Biophysics, Center for Stem Cell Biology, Vanderbilt University, Nashville, TN, USA.
Maike SanderDepartment of Pediatrics and Cellular and Molecular Medicine, University of California, San Diego, CA, USA.
Christopher E V WrightDepartment of Cell and Developmental Biology, Program in Developmental Biology and Center for Stem Cell Biology, Vanderbilt University School of Medicine, Nashville, TN, USA.
Melissa K ThomasLilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN, USA.
Kenichiro FuruyamaDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Simona CheraDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Pedro L HerreraDepartment of Genetic Medicine and Development, iGE3 and Centre facultaire du diabète, Faculty of Medicine, University of Geneva, Geneva, Switzerland. pedro.herrera@unige.ch.ORCID http://orcid.org/0000-0003-0771-9504
University of Geneva · CHVanderbilt University · USEli Lilly (United States) · USJuntendo University · JPThe University of Osaka · JPUniversity of California San Diego · US

Funding

Coordinating Center for Beta Cell Biology ConsortiumU01DK072473 · NIDDK · VANDERBILT UNIVERSITY · PI MAGNUSON, MARK A · 2005 to 2014
$61.0M
Nkx6 gene function in pancreas developmentR01DK068471 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI WORTHAM, MATTHEW · 2004 to 2024
$6.6M
Single-Cell Analyses of Human Islets in T1D Using Highly Multiplexed ImagingUC4DK108132 · NIDDK · UNIVERSITY OF FLORIDA · PI ATKINSON, MARK A., BODENMILLER, BERND · 2015 to 2015
$3.6M
Beta-cell Regeneration by Islet Cell Type Interconversion: Exploiting Islet Cell Plasticity for Diabetes RecoveryUC4DK104209 · NIDDK · UNIVERSITY OF GENEVA · PI HERRERA, PEDRO L · 2014 to 2014
$2.4M
Beta Cell Regeneration by Reprogramming of Adult Pancreatic CellsU01DK089566 · NIDDK · UNIVERSITY OF GENEVA · PI HERRERA, PEDRO L · 2010 to 2014
$1.0M
NIDDK NIH HHS R01 DK068471NIDDK NIH HHS U01 DK072473NIDDK NIH HHS U01 DK089566NIDDK NIH HHS UC4 DK104209NIDDK NIH HHS UC4 DK108132
6 · The paper itself

Abstract

The mechanisms that restrict regeneration and maintain cell identity following injury are poorly characterized in higher vertebrates. Following β-cell loss, 1-2% of the glucagon-producing α-cells spontaneously engage in insulin production in mice. Here we explore the mechanisms inhibiting α-cell plasticity. We show that adaptive α-cell identity changes are constrained by intra-islet insulin- and Smoothened-mediated signalling, among others. The combination of β-cell loss or insulin-signalling inhibition, with Smoothened inactivation in α- or δ-cells, stimulates insulin production in more α-cells. These findings suggest that the removal of constitutive 'brake signals' is crucial to neutralize the refractoriness to adaptive cell-fate changes. It appears that the maintenance of cell identity is an active process mediated by repressive signals, which are released by neighbouring cells and curb an intrinsic trend of differentiated cells to change.

Indexed as

Signal TransductionAnimalsCell DifferentiationCell PlasticityCell ProliferationFemaleGlucagon-Secreting CellsInsulinInsulin-Secreting CellsIslets of LangerhansMaleMice, Inbred C57BLMice, KnockoutMice, SCIDMice, TransgenicSmoothened ReceptorInsulinSmoothened ReceptorSmo protein, mouse

Identifiers

PMID30361701
PMCPMC6215453
OpenAlexW2897204017

What OpenQuestion holds

Textmetadata
LicenceTDM
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.