Evidence map›Paper›PMID 42635265›Full record

ReviewDevelopment (Cambridge, England)2026

Biophysics of lumen morphogenesis.

Byung Ho Lee, Markus Mukenhirn, Tristan Guyomar, Yann Maggipinto, Sakurako Tanida, Kana Fuji, Linjie Lu, Felix Romer, Makiko Nonomura, Tetsuya Hiraiwa and 4 more

Abstract readReview
In one paragraph

Review in Development (Cambridge, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Mechanics of compression-driven morphogenesis.Development (Cambridge, England) · 2026
    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

14 authors.

Byung Ho LeeMax Planck Institute of Molecular Cell Biology and Genetics, Dresden 01307, Germany.
Markus MukenhirnTechnische Universität Dresden, Biotechnologisches Zentrum, Center for Molecular and Cellular Bioengineering (CMCB), Dresden 01307, Germany.
Tristan GuyomarInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch 67404, France.
Yann MaggipintoInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch 67404, France.
Sakurako TanidaUniversal Biology Institute, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan.
Kana FujiUniversal Biology Institute, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan.
Linjie LuInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch 67404, France.
Felix RomerMax Planck Institute of Molecular Cell Biology and Genetics, Dresden 01307, Germany.ORCID 0009-0008-4738-559X
Makiko NonomuraDepartment of Mathematical Information Engineering, College of Industrial Technology, Nihon University, Chiba 275-8576, Japan.
Tetsuya HiraiwaInstitute of Physics, Academia Sinica, Taipei 11529, Taiwan.
Masaki SanoUniversal Biology Institute, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan.
Alf HonigmannTechnische Universität Dresden, Biotechnologisches Zentrum, Center for Molecular and Cellular Bioengineering (CMCB), Dresden 01307, Germany.
Daniel RivelineInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch 67404, France.
Anne Grapin-BottonMax Planck Institute of Molecular Cell Biology and Genetics, Dresden 01307, Germany.ORCID 0000-0002-1202-5235

Funding

Agence Nationale de la RechercheCentre national de la recherche scientifiqueFondation pour la Recherche MédicaleHuman Frontier Science Program RGP0050/2018Institut National de la Santé et de la Recherche Médicale ANR-10-IDEX-0002Institut National de la Santé et de la Recherche Médicale ANR-17-EURE-0023Institut National de la Santé et de la Recherche Médicale ANR 20-SFRI-0012Max Planck SocietyMechanobiology Institute, SingaporeNational Natural Science Foundation of China 12174254National Natural Science Foundation of China 12250710131Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung P2GEP3-181529Université de Strasbourg
6 · The paper itself

Abstract

Although lumen formation is a key feature of organogenesis, luminal compartments - formed through the secretion of fluid, ions and macromolecules by the cells, usually on the apical side - are often viewed as passive by-products of epithelial polarity. Here, we discuss how luminal fluids actively contribute to morphogenesis in metazoans through mechanical, hydraulic and electrochemical interactions with the surrounding epithelia and the extracellular matrix (ECM). We first outline the diversity of lumen architectures and summarize conserved mechanisms of lumen nucleation, fusion, folding and growth across metazoans. We then present the physical principles governing lumen morphogenesis, highlighting how hydrostatic and osmotic pressures, cortical tension and matrix mechanics interact to shape tissues. Furthermore, theoretical modeling and numerical simulations provide a quantitative framework for predicting phenotypes related to lumen shape, exploring the parameter space of hydraulic and active tissue mechanics variables, and linking molecular perturbations to emergent tissue geometries. Finally, we examine feedback loops whereby lumen-associated forces regulate junctional integrity, proliferation, differentiation and tissue patterning. Together, these concepts position luminal fluids as active regulators of lumen morphogenesis.

Indexed as

BiophysicsMorphogenesisOrganogenesisAnimalsBiophysical PhenomenaEpitheliumExtracellular MatrixHumansModels, BiologicalBiological physicsEpitheliaExtracellular matrixLumenOrganogenesis

Identifiers

PMID42635265
PMCPMC13571819

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.