Evidence map›Paper›PMID 29101840›Full record

ArticleAtherosclerosis2017

Ex vivo culture of human atherosclerotic plaques: A model to study immune cells in atherogenesis.

Anna Lebedeva, Daria Vorobyeva, Murad Vagida, Oxana Ivanova, Eugeny Felker, Wendy Fitzgerald, Natalya Danilova, Vladimir Gontarenko, Alexander Shpektor, Elena Vasilieva and 1 more

Open access · greenAbstract read
In one paragraph

Article in Atherosclerosis, 2017. 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
1.2field-weighted citation impact, top 22% 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, 32 citations in OpenAlex.

  1. Review
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  7. Cytokine production in anFrontiers in immunology · 2024
    Article
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  10. Divergence of acetate uptake in proinflammatory and inflammation-resolving macrophages: implications for imaging atherosclerosis.Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology · 2022
    Article
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  15. Adaptive Immune Responses in Human Atherosclerosis.International journal of molecular sciences · 2020
    Review
  16. Article
  17. Article
  18. IL-22 produced by Th22 cells aggravates atherosclerosis development in ApoEJournal of cellular and molecular medicine · 2020
    Article
  19. 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

11 authors at 4 institutions in 2 countries.

Anna LebedevaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Daria VorobyevaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Murad VagidaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Oxana IvanovaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Eugeny FelkerLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Wendy FitzgeraldSection on Intercellular Interactions, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
Natalya DanilovaDepartment of Clinical Pathology, Lomonosov Moscow State University, Moscow, Russia.
Vladimir GontarenkoDepartment of Vascular Surgery, A.V. Vishnevsky Institute of Surgery, Moscow, Russia.
Alexander ShpektorLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Elena VasilievaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia. Electronic address: vasilieva.helena@gmail.com.
Leonid MargolisSection on Intercellular Interactions, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
Moscow State University of Medicine and Dentistry · RUNational Institutes of Health · USLomonosov Moscow State University · RUNational Medical Research Center of Surgery named after A. Vishnevsky · RU

Funding

Cell Interactions in Three Dimensional Tissue CultureZIAHD001416 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI MARGOLIS, LEONID B. · 2009 to 2017
$15.7M
Viral transmission and pathogenesis in human tissuesZIAHD008968 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI MARGOLIS, LEONID B. · 2018 to 2023
$12.2M
TISSUE IMAGING IN CELL BIOLOGYZ01HD001416 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI MARGOLIS, LEONID B. · 1993 to 2008
$2.7M
Intramural NIH HHS Z01 HD001416Intramural NIH HHS Z99 HD999999
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe mechanisms that drive atherosclerotic plaque progression and destabilization in humans remain largely unknown. Laboratory models are needed to study these mechanisms under controlled conditions. The aim of this study was to establish a new ex vivo model of human atherosclerotic plaques that preserves the main cell types in plaques and the extracellular components in the context of native cytoarchitecture.

methodsAtherosclerotic plaques from carotid arteries of 28 patients undergoing carotid endarterectomy were dissected and cultured. At various time-points, samples were collected and analysed histologically. After enzymatic digestion, single cells were analysed with flow cytometry. Moreover, tissue cytokine production was evaluated.

resultsWe optimised the plaque dissection protocol by cutting plaques into circular segments that we cultured on collagen rafts at the medium-air interface, thus keeping them well oxygenated. With this technique, the relative presence of T and B lymphocytes did not change significantly during culture, and the sizes of lymphocyte subsets remained stable after day 4 of culture. Macrophages, smooth muscle cells, and fibroblasts with collagen fibres, as well as T and B lymphocyte subsets and CD16 natural killer cells, remained largely preserved for 19 days of culture, with a continuous production of inflammatory cytokines and chemokines.

conclusionsOur new model of ex vivo human atherosclerotic plaques, which preserves the main subsets of immune cells in the context of tissue cytoarchitecture, may be used to investigate important aspects of atherogenesis, in particular, the functions of immune cells under controlled laboratory conditions.

Indexed as

AgedAtherosclerosisB-LymphocytesCarotid ArteriesChemokinesCytokinesEndarterectomy, CarotidFemaleFlow CytometryGPI-Linked ProteinsHumansImmune SystemImmunohistochemistryIn Vitro TechniquesMacrophagesMaleChemokinesCytokinesFCGR3B protein, humanGPI-Linked ProteinsReceptors, IgGAtherosclerosisAtherosclerotic plaqueCytokineImmune systemLymphocyteTissue culture

Identifiers

PMID29101840
PMCPMC5811192
OpenAlexW2763384674

What OpenQuestion holds

Textmetadata
LicenceTDM
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.