Evidence map›Paper›PMID 35196500›Full record

ArticleCell2022

Cell surface fluctuations regulate early embryonic lineage sorting.

Ayaka Yanagida, Elena Corujo-Simon, Christopher K Revell, Preeti Sahu, Giuliano G Stirparo, Irene M Aspalter, Alex K Winkel, Ruby Peters, Henry De Belly, Davide A D Cassani and 7 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
7.7field-weighted citation impact, top 1% of its field
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

44 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
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  8. Review
  9. Adhesion-regulated dynamics of cells.Biophysical journal · 2025
    Article
  10. Article
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  12. A thermodynamic perspective on mammalian neural crest ingression.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Ayaka YanagidaWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK; Living Systems Institute, University of Exeter, Exeter EX4 4QD, UK.
Elena Corujo-SimonWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK.
Christopher K RevellCavendish Laboratory, Department of Physics, University of Cambridge, JJ Thomson Ave, Cambridge CB3 0HE, UK.
Preeti SahuInstitute of Science and Technology Austria, Am Campus 1, Klosterneuburg 3400, Austria.
Giuliano G StirparoWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK.
Irene M AspalterMRC Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK.
Alex K WinkelDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
Ruby PetersDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
Henry De BellyWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK; MRC Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
Davide A D CassaniMRC Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK.
Sarra AchouriWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
Raphael BlumenfeldGonville & Caius College, University of Cambridge, Trinity St., Cambridge CB2 1TA, UK.
Kristian FranzeDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
Edouard HannezoInstitute of Science and Technology Austria, Am Campus 1, Klosterneuburg 3400, Austria.
Ewa K PaluchMRC Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK. Electronic address: ekp25@cam.ac.uk.
Jennifer NicholsWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK; Centre for Trophoblast Research, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK. Electronic address: jenny.nichols@ed.ac.uk.
Kevin J ChalutWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK. Electronic address: kc370@cam.ac.uk.
Wellcome/MRC Cambridge Stem Cell Institute · GBUniversity of Cambridge · GBInstitute of Science and Technology Austria · ATMRC Laboratory for Molecular Cell Biology · GB

Funding

Biotechnology and Biological Sciences Research Council BB/MOO4023/1Biotechnology and Biological Sciences Research Council BB/R000042Biotechnology and Biological Sciences Research Council BB/T007044/1Medical Research Council MC_PC_17230Medical Research Council MC_UU_00012/5Medical Research Council MC_UU_12018/5Wellcome TrustWellcome Trust 203151/Z/16/Z
6 · The paper itself

Abstract

In development, lineage segregation is coordinated in time and space. An important example is the mammalian inner cell mass, in which the primitive endoderm (PrE, founder of the yolk sac) physically segregates from the epiblast (EPI, founder of the fetus). While the molecular requirements have been well studied, the physical mechanisms determining spatial segregation between EPI and PrE remain elusive. Here, we investigate the mechanical basis of EPI and PrE sorting. We find that rather than the differences in static cell surface mechanical parameters as in classical sorting models, it is the differences in surface fluctuations that robustly ensure physical lineage sorting. These differential surface fluctuations systematically correlate with differential cellular fluidity, which we propose together constitute a non-equilibrium sorting mechanism for EPI and PrE lineages. By combining experiments and modeling, we identify cell surface dynamics as a key factor orchestrating the correct spatial segregation of the founder embryonic lineages.

Indexed as

BlastocystEmbryo, MammalianEndodermAnimalsCell DifferentiationCell LineageCell MembraneEmbryonic DevelopmentMammalsMiceProtein Transportcell sortingcell surface dynamicscell surface mechanicsembryo developmentlineage segregationmorphogenesis

Identifiers

PMID35196500
PMCPMC8896887
OpenAlexW4220963742

What OpenQuestion holds

Textmetadata
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.