Evidence map›Paper›PMID 25786211›Full record

ArticlePLoS biology2015

Cell cycle-dependent differentiation dynamics balances growth and endocrine differentiation in the pancreas.

Yung Hae Kim, Hjalte List Larsen, Pau Rué, Laurence A Lemaire, Jorge Ferrer, Anne Grapin-Botton

Abstract read
In one paragraph

Article in PLoS biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Imaging developmental cell cycles.Biophysical journal · 2021
    Review
  10. Islets · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Modelling the endocrine pancreas in health and disease.Nature reviews. Endocrinology · 2019
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  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

6 authors.

Yung Hae KimDanStem, University of Copenhagen, Copenhagen, Denmark; Ecole Polytechnique Fédérale de Lausanne, Life Sciences, Institute of Bioengineering, Lausanne, Switzerland.
Hjalte List LarsenDanStem, University of Copenhagen, Copenhagen, Denmark.
Pau RuéDepartment of Genetics, University of Cambridge, Cambridge, United Kingdom.
Laurence A LemaireDanStem, University of Copenhagen, Copenhagen, Denmark.
Jorge FerrerDepartment of Medicine, Imperial College London, London, United Kingdom; Institut d'Investigacions August Pi i Sunyer, CIBER de Diabetes y Enfermedades Metabólicas Asociadas, Barcelona, Spain.
Anne Grapin-BottonDanStem, University of Copenhagen, Copenhagen, Denmark; Ecole Polytechnique Fédérale de Lausanne, Life Sciences, Institute of Bioengineering, Lausanne, Switzerland.

Funding

Architecture and communication controlling the efficient generation of beta cellsU01DK089570 · NIDDK · VANDERBILT UNIVERSITY · PI WRIGHT, CHRISTOPHER V · 2010 to 2014
$5.5M
Medical Research Council MR/L02036X/1NIDDK NIH HHS 1U01DK089570-01NIDDK NIH HHS U01 DK089570Wellcome Trust 101033
6 · The paper itself

Abstract

Organogenesis relies on the spatiotemporal balancing of differentiation and proliferation driven by an expanding pool of progenitor cells. In the mouse pancreas, lineage tracing at the population level has shown that the expanding pancreas progenitors can initially give rise to all endocrine, ductal, and acinar cells but become bipotent by embryonic day 13.5, giving rise to endocrine cells and ductal cells. However, the dynamics of individual progenitors balancing self-renewal and lineage-specific differentiation has never been described. Using three-dimensional live imaging and in vivo clonal analysis, we reveal the contribution of individual cells to the global behaviour and demonstrate three modes of progenitor divisions: symmetric renewing, symmetric endocrinogenic, and asymmetric generating a progenitor and an endocrine progenitor. Quantitative analysis shows that the endocrine differentiation process is consistent with a simple model of cell cycle-dependent stochastic priming of progenitors to endocrine fate. The findings provide insights to define control parameters to optimize the generation of β-cells in vitro.

Indexed as

Acinar CellsAnimalsBasic Helix-Loop-Helix ProteinsCell CycleCell DifferentiationCell LineageCell ProliferationCell TrackingEmbryo, MammalianGene Expression Regulation, DevelopmentalGenes, ReporterGreen Fluorescent ProteinsHomeodomain ProteinsImage Processing, Computer-AssistedInsulin-Secreting CellsLuminescent ProteinsBasic Helix-Loop-Helix ProteinsGreen Fluorescent ProteinsHomeodomain ProteinsLuminescent ProteinsNerve Tissue ProteinsNeurog3 protein, mousepancreatic and duodenal homeobox 1 proteinRed Fluorescent ProteinSox9 protein, mouseSOX9 Transcription FactorTrans-Activators

Identifiers

PMID25786211
PMCPMC4364879

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.