Evidence map›Paper›PMID 30970663›Full record

ArticleCells2019

Flow Cytometry-Based Characterization of Mast Cells in Human Atherosclerosis.

Eva Kritikou, Marie A C Depuydt, Margreet R de Vries, Kevin E Mulder, Arthur M Govaert, Marrit D Smit, Janine van Duijn, Amanda C Foks, Anouk Wezel, Harm J Smeets and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Role of Mast Cells in Eosinophilic Gastrointestinal Diseases.Immunology and allergy clinics of North America · 2024
    Review
  6. Article
  7. Mast Cells in Cardiac Remodeling: Focus on the Right Ventricle.Journal of cardiovascular development and disease · 2024
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Inflammatory Cells in Atherosclerosis.Antioxidants (Basel, Switzerland) · 2022
    Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Mast Cells in Cardiovascular Disease: From Bench to Bedside.International journal of molecular sciences · 2019
    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

14 authors at 3 institutions in 1 country.

Eva KritikouDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. e.kritikou@lacdr.leidenuniv.nl.
Marie A C DepuydtDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. m.a.c.depuydt@lacdr.leidenuniv.nl.
Margreet R de VriesDepartment of Surgery, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands. m.r.de_vries@lumc.nl.
Kevin E MulderDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. kevin.evan@hotmail.com.
Arthur M GovaertDepartment of Surgery, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands. a.m.govaert@lumc.nl.
Marrit D SmitDepartment of Surgery, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands. m.d.smit@lumc.nl.
Janine van DuijnDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. a.c.foks@lacdr.leidenuniv.nl.
Amanda C FoksDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. a.c.foks@lacdr.leidenuniv.nl.
Anouk WezelDepartment of Surgery, HMC Westeinde, 2512 VA The Hague, The Netherlands. a.wezel@haaglandenmc.nl.
Harm J SmeetsDepartment of Surgery, HMC Westeinde, 2512 VA The Hague, The Netherlands. h.smeets@haaglandenmc.nl.
Bram SlütterDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. b.a.slutter@lacdr.leidenuniv.nl.
Paul H A QuaxDepartment of Surgery, Leiden University Medical Center, 2333 ZC Leiden, The Netherlands. p.h.a.quax@lumc.nl.
Johan KuiperDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. j.kuiper@lacdr.leidenuniv.nl.
Ilze BotDivision of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, 2333 CC Leiden, The Netherlands. i.bot@lacdr.leidenuniv.nl.
Leiden University · NLLeiden University Medical Center · NLMedisch Centrum Haaglanden · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of mast cells in human atherosclerotic plaques has been associated with adverse cardiovascular events. Mast cell activation, through the classical antigen sensitized-IgE binding to their characteristic Fcε-receptor, causes the release of their cytoplasmic granules. These granules are filled with neutral proteases such as tryptase, but also with histamine and pro-inflammatory mediators. Mast cells accumulate in high numbers within human atherosclerotic tissue, particularly in the shoulder region of the plaque. These findings are largely based on immunohistochemistry, which does not allow for the extensive characterization of these mast cells and of the local mast cell activation mechanisms. In this study, we thus aimed to develop a new flow-cytometry based methodology in order to analyze mast cells in human atherosclerosis. We enzymatically digested 22 human plaque samples, collected after femoral and carotid endarterectomy surgery, after which we prepared a single cell suspension for flow cytometry. We were able to identify a specific mast cell population expressing both CD117 and the FcεR, and observed that most of the intraplaque mast cells were activated based on their CD63 protein expression. Furthermore, most of the activated mast cells had IgE fragments bound on their surface, while another fraction showed IgE-independent activation. In conclusion, we are able to distinguish a clear mast cell population in human atherosclerotic plaques, and this study establishes a strong relationship between the presence of IgE and the activation of mast cells in advanced atherosclerosis. Our data pave the way for potential therapeutic intervention through targeting IgE-mediated actions in human atherosclerosis.

Indexed as

AtherosclerosisCells, CulturedFlow CytometryHumansImmunoglobulin EMast CellsPlaque, AtheroscleroticProto-Oncogene Proteins c-kitReceptors, IgETetraspanin 30CD63 protein, humanImmunoglobulin EKIT protein, humanProto-Oncogene Proteins c-kitReceptors, IgETetraspanin 30atherosclerosisflow cytometrymast cellplaque stabilitytryptase

Identifiers

PMID30970663
PMCPMC6523866
OpenAlexW2940370793

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.