Evidence map›Paper›PMID 41419573›Full record

ArticleNature cell biology2026

Permeability-driven pressure and cell proliferation control lumen morphogenesis in pancreatic organoids.

Byung Ho Lee, Kana Fuji, Heike Petzold, Phil Seymour, Siham Yennek, Coline Schewin, Allison Lewis, Daniel Riveline, Tetsuya Hiraiwa, Masaki Sano and 1 more

Abstract read
In one paragraph

Article in Nature cell biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Mechanics of compression-driven morphogenesis.Development (Cambridge, England) · 2026
    Review
  4. Biophysics of lumen morphogenesis.Development (Cambridge, England) · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Review
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

11 authors.

Byung Ho LeeMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany. blee@mpi-cbg.de.ORCID http://orcid.org/0000-0002-5837-7914
Kana FujiUniversal Biology Institute, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
Heike PetzoldMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.ORCID http://orcid.org/0000-0001-9518-4989
Phil SeymourThe Novo Nordisk Foundation Center for Stem Cell Biology, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-5782-6020
Siham YennekThe Novo Nordisk Foundation Center for Stem Cell Biology, Copenhagen, Denmark.
Coline SchewinMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Allison LewisMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Daniel RivelineIGBMC, Université de Strasbourg, CNRS, INSERM, Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.ORCID http://orcid.org/0000-0002-4632-011X
Tetsuya HiraiwaUniversal Biology Institute, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
Masaki SanoUniversal Biology Institute, Graduate School of Science, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0002-6262-9635
Anne Grapin-BottonMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany. botton@mpi-cbg.de.ORCID http://orcid.org/0000-0002-1202-5235

Funding

Human Frontier Science Program (HFSP) RGP0050/2018
6 · The paper itself

Abstract

Lumen formation in organ epithelia involves processes such as polarization, secretion, exocytosis and contractility, but what controls lumen shape remains unclear. Here we study how lumina develop spherical or complex structures using pancreatic organoids. Combining computational phase-field modelling and experiments, we found that lumen morphology depends on the balance between cell cycle duration and lumen pressure, low pressure and high proliferation produce complex shapes. Manipulating proliferation and lumen pressure can alter or reverse lumen development both in silico and in vitro. Increasing epithelial permeability reduces lumen pressure, converting from spherical to complex lumina. During pancreas development, the epithelium is initially permeable and becomes sealed, experimentally increasing permeability at late stages impairs ductal morphogenesis. Overall, our work underscores how proliferation, pressure and permeability orchestrate lumen shape, offering insights for tissue engineering and cystic disease treatment.

Indexed as

Cell ProliferationMorphogenesisOrganoidsPancreasAnimalsEpithelial CellsHumansMicePancreatic DuctsPermeabilityPressure

Identifiers

PMID41419573
PMCPMC12807866

What OpenQuestion holds

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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.