Evidence map›Paper›PMID 27807273›Full record

ArticleJournal of the Royal Society, Interface2016

A new mechanism for spatial pattern formation via lateral and protrusion-mediated lateral signalling.

Zena Hadjivasiliou, Ginger L Hunter, Buzz Baum

Open access · hybridAbstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Quantifying bristle cell organization inbioRxiv : the preprint server for biology · 2025
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  5. Article
  6. Article
  7. Article
  8. Information content and optimization of self-organized developmental systems.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Dynamic switching of lateral inhibition spatial patterns.Journal of the Royal Society, Interface · 2022
    Article
  15. Article
  16. Notch signaling sculpts the stem cell niche.Frontiers in cell and developmental biology · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. Notch Signalling in Breast Development and Cancer.Frontiers in cell and developmental biology · 2021
    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

3 authors at 2 institutions in 1 country.

Zena HadjivasiliouCentre for Mathematics, Physics, and Engineering in the Life Sciences and Experimental Biology, University College London, London WC1E 6BT, UK zena.hadjivasiliou@unige.ch.ORCID 0000-0003-1174-1421
Ginger L HunterMRC-Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK.
Buzz BaumMRC-Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK.
MRC Laboratory for Molecular Cell Biology · GBUniversity College London · GB

Funding

BBSRC BB/J008532/1Biotechnology and Biological Sciences Research Council BB/J008532/1Cancer Research UKMedical Research Council
6 · The paper itself

Abstract

Tissue organization and patterning are critical during development when genetically identical cells take on different fates. Lateral signalling plays an important role in this process by helping to generate self-organized spatial patterns in an otherwise uniform collection of cells. Recent data suggest that lateral signalling can be mediated both by junctional contacts between neighbouring cells and via cellular protrusions that allow non-neighbouring cells to interact with one another at a distance. However, it remains unclear precisely how signalling mediated by these distinct types of cell-cell contact can physically contribute to the generation of complex patterns without the assistance of diffusible morphogens or pre-patterns. To explore this question, in this work we develop a model of lateral signalling based on a single receptor/ligand pair as exemplified by Notch and Delta. We show that allowing the signalling kinetics to differ at junctional versus protrusion-mediated contacts, an assumption inspired by recent data which show that the cleavage of Notch in several systems requires both Delta binding and the application of mechanical force, permits individual cells to act to promote both lateral activation and lateral inhibition. Strikingly, under this model, in which Delta can sequester Notch, a variety of patterns resembling those typical of reaction-diffusion systems is observed, together with more unusual patterns that arise when we consider changes in signalling kinetics, and in the length and distribution of protrusions. Importantly, these patterns are self-organizing-so that local interactions drive tissue-scale patterning. Together, these data show that protrusions can, in principle, generate different types of patterns in addition to contributing to long-range signalling and to pattern refinement.

Indexed as

Models, BiologicalAnimalsCell CommunicationCell Membrane StructuresHumansIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchSignal Transductiondelta proteinIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchDeltalateral inhibitionNotchpatterningprotrusion signalling

Identifiers

PMID27807273
PMCPMC5134009
OpenAlexW2547596230

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.