Evidence map›Paper›PMID 30563863›Full record

ArticleScience signaling2018

CD45 exclusion- and cross-linking-based receptor signaling together broaden FcεRI reactivity.

James H Felce, Erdinc Sezgin, Madina Wane, Heather Brouwer, Michael L Dustin, Christian Eggeling, Simon J Davis

Abstract read
In one paragraph

Article in Science signaling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. CD6-mediated inhibition of T cell activation via modulation of Ras.Cell communication and signaling : CCS · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. NADTheranostics · 2022
    Article
  15. Regulation of myeloid-cell activation.Current opinion in immunology · 2021
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Molecular height measurement by cell surface optical profilometry (CSOP).Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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

7 authors.

James H FelceMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.ORCID 0000-0001-5531-9244
Erdinc SezginMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.ORCID 0000-0002-4915-388X
Madina WaneMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.ORCID 0000-0002-7647-0194
Heather BrouwerMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.ORCID 0000-0003-3840-6834
Michael L DustinKennedy Institute of Rheumatology, University of Oxford, Oxford OX3 7FY, UK. simon.davis@imm.ox.ac.uk christian.eggeling@rdm.ox.ac.uk michael.dustin@kennedy.ox.ac.uk.ORCID 0000-0003-4983-6389
Christian EggelingMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK. simon.davis@imm.ox.ac.uk christian.eggeling@rdm.ox.ac.uk michael.dustin@kennedy.ox.ac.uk.ORCID 0000-0002-3698-5599
Simon J DavisMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK. simon.davis@imm.ox.ac.uk christian.eggeling@rdm.ox.ac.uk michael.dustin@kennedy.ox.ac.uk.ORCID 0000-0002-2280-1170

Funding

Medical Research Council MC_UU_00008/4Medical Research Council MC_UU_00008/9Medical Research Council MC_UU_12010/4Medical Research Council MC_UU_12010/9Medical Research Council MC_UU_12025Medical Research Council MR/K01577X/1Wellcome Trust 091911Wellcome Trust 098274/Z/12/ZWellcome Trust 100262/Z/12/ZWellcome Trust 104924/14/Z/14Wellcome Trust 107375/Z/15/ZWellcome Trust 207547Wellcome Trust 207547/Z/17/Z
6 · The paper itself

Abstract

For many years, the high-affinity receptor for immunoglobulin E (IgE) FcεRI, which is expressed by mast cells and basophils, has been widely held to be the exemplar of cross-linking (that is, aggregation dependent) signaling receptors. We found, however, that FcεRI signaling could occur in the presence or absence of receptor cross-linking. Using both cell and cell-free systems, we showed that FcεRI signaling was stimulated by surface-associated monovalent ligands through the passive, size-dependent exclusion of the receptor-type tyrosine phosphatase CD45 from plasma membrane regions of FcεRI-ligand engagement. Similarly to the T cell receptor, FcεRI signaling could also be initiated in a ligand-independent manner. These data suggest that a simple mechanism of CD45 exclusion-based receptor triggering could function together with cross-linking-based FcεRI signaling, broadening mast cell and basophil reactivity by enabling these cells to respond to both multivalent and surface-presented monovalent antigens. These findings also strengthen the case that a size-dependent, phosphatase exclusion-based receptor triggering mechanism might serve generally to facilitate signaling by noncatalytic immune receptors.

Indexed as

Cell DegranulationAnimalsCRISPR-Cas SystemsCross-Linking ReagentsImmunoglobulin EIntegrinsLeukemia, Basophilic, AcuteLeukocyte Common AntigensMast CellsRatsReceptors, IgETumor Cells, CulturedCross-Linking ReagentsFCER1A protein, ratImmunoglobulin EIntegrinsLeukocyte Common AntigensPtprc protein, ratReceptors, IgE

Identifiers

PMID30563863
PMCPMC7612966

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Registered trials

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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.