Evidence map›Paper›PMID 35365816›Full record

ReviewNature reviews. Molecular cell biology2022

Interplay between mechanics and signalling in regulating cell fate.

Henry De Belly, Ewa K Paluch, Kevin J Chalut

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Molecular cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 144 papers.

0numbers the graph read from it
0cells of the map it votes in
144citing 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

144 citing papers in PubMed.

  1. Article
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  3. SEC Mediates mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  13. Biophysics of lumen morphogenesis.Development (Cambridge, England) · 2026
    Review
  14. Article
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  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

84 more citing papers are in PubMed but not listed here.

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

3 authors.

Henry De BellyDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Ewa K PaluchDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK. ekp25@cam.ac.uk.ORCID http://orcid.org/0000-0003-4691-2323
Kevin J ChalutDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK. kc370@cam.ac.uk.ORCID http://orcid.org/0000-0001-6200-9690

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanical signalling affects multiple biological processes during development and in adult organisms, including cell fate transitions, cell migration, morphogenesis and immune responses. Here, we review recent insights into the mechanisms and functions of two main routes of mechanical signalling: outside-in mechanical signalling, such as mechanosensing of substrate properties or shear stresses; and mechanical signalling regulated by the physical properties of the cell surface itself. We discuss examples of how these two classes of mechanical signalling regulate stem cell function, as well as developmental processes in vivo. We also discuss how cell surface mechanics affects intracellular signalling and, in turn, how intracellular signalling controls cell surface mechanics, generating feedback into the regulation of mechanosensing. The cooperation between mechanosensing, intracellular signalling and cell surface mechanics has a profound impact on biological processes. We discuss here our understanding of how these three elements interact to regulate stem cell fate and development.

Indexed as

Biological PhenomenaMechanotransduction, CellularCell DifferentiationMorphogenesisSignal Transduction

Identifiers

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.