Evidence map›Paper›PMID 39467136›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Capturing the mechanosensitivity of cell proliferation in models of epithelium.

Kevin Höllring, Lovro Nuić, Luka Rogić, Sara Kaliman, Simone Gehrer, Carina Wollnik, Florian Rehfeldt, Maxime Hubert, Ana-Sunčana Smith

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. On the control of cell proliferation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Capturing the mechanosensitivity of cell proliferation in models of epithelium.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Kevin HöllringPhysics Underlying Life Sciences Group, Department of Physics, Interdisciplinary Center for Nanostructured Films, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen 91058, Germany.ORCID 0000-0002-9497-3254
Lovro NuićGroup for Computational Life Sciences, Division of Physical Chemistry, Ruđer Bošković Institute, Zagreb 10000, Croatia.
Luka RogićGroup for Computational Life Sciences, Division of Physical Chemistry, Ruđer Bošković Institute, Zagreb 10000, Croatia.
Sara KalimanPhysics Underlying Life Sciences Group, Department of Physics, Interdisciplinary Center for Nanostructured Films, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen 91058, Germany.ORCID 0009-0003-7027-2669
Simone GehrerPhysics Underlying Life Sciences Group, Department of Physics, Interdisciplinary Center for Nanostructured Films, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen 91058, Germany.
Carina WollnikFaculty of Physics, University of Göttingen, Third Institute of Physics-Biophysics, Göttingen 37077, Germany.ORCID 0009-0000-0964-3051
Florian RehfeldtFaculty of Physics, University of Göttingen, Third Institute of Physics-Biophysics, Göttingen 37077, Germany.ORCID 0000-0001-9086-3835
Maxime HubertPhysics Underlying Life Sciences Group, Department of Physics, Interdisciplinary Center for Nanostructured Films, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen 91058, Germany.ORCID 0000-0001-9412-372X
Ana-Sunčana SmithPhysics Underlying Life Sciences Group, Department of Physics, Interdisciplinary Center for Nanostructured Films, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen 91058, Germany.ORCID 0000-0002-0835-0086

Funding

Deutsche Forschungsgemeinschaft (DFG) RTG 1962Deutsche Forschungsgemeinschaft (DFG) RTG 2415Deutsche Forschungsgemeinschaft (DFG) SFB 755EC | European Research Council (ERC) StG 337593
6 · The paper itself

Abstract

Despite the primary role of cell proliferation in tissue development and homeostatic maintenance, the interplay between cell density, cell mechanoresponse, and cell growth and division is not yet understood. In this article, we address this issue by reporting on an experimental investigation of cell proliferation on all time- and length-scales of the development of a model tissue, grown on collagen-coated glass or deformable substrates. Through extensive data analysis, we demonstrate the relation between mechanoresponse and probability for cell division, as a function of the local cell density. Motivated by these results, we construct a minimal model of cell division in tissue environment that can recover the data. By parameterizing the growth and the dividing phases of the cell cycle, and introducing such a proliferation model in dissipative particle dynamics simulations, we recover the mechanoresponsive, time-dependent density profiles in 2D tissues growing to macroscopic scales. The importance of separating the cell population into growing and dividing cells, each characterized by a particular time scale, is further emphasized by calculations of density profiles based on adapted Fisher-Kolmogorov equations. Together, these results show that the mechanoresponse on the level of a constitutive cell and its proliferation results in a matrix-sensitive active pressure. The latter evokes massive cooperative displacement of cells in the invading tissue and is a key factor for developing large-scale structures in the steady state.

Indexed as

Cell ProliferationMechanotransduction, CellularModels, BiologicalAnimalsCell CycleCell DivisionEpitheliumcell division in tissue environmentdissipative particle dynamicsepithelial tissueFisher–Kolmogorov equation

Identifiers

PMID39467136
PMCPMC11551403

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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.