Evidence map›Paper›PMID 27658051›Full record

ArticlePloS one

CD11c/CD18 Dominates Adhesion of Human Monocytes, Macrophages and Dendritic Cells over CD11b/CD18.

Noémi Sándor, Szilvia Lukácsi, Rita Ungai-Salánki, Norbert Orgován, Bálint Szabó, Róbert Horváth, Anna Erdei, Zsuzsa Bajtay

Open access · goldAbstract read
In one paragraph

Article in PloS one. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

52 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
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  3. Adhesion forces between macrophages and cancer cells promote early tumor development.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  17. Toll-like receptors and integrins crosstalk.Frontiers in immunology · 2024
    Review
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Noémi SándorMTA-ELTE Immunology Research Group, Hungarian Academy of Sciences, Budapest, Hungary.ORCID http://orcid.org/0000-0002-2461-1389
Szilvia LukácsiDepartment of Immunology, Institute of Biology, Faculty of Science, Eötvös Loránd University, Budapest, Hungary.
Rita Ungai-SalánkiDepartment of Biological Physics, Institute of Physics, Faculty of Science, Eötvös Loránd University, Budapest, Hungary.
Norbert OrgovánNanobiosensorics "Lendület" Group, Institute of Technical Physics and Material Sciences, Centre for Energy Research, Hungarian Academy of Sciences, Budapest, Hungary.
Bálint SzabóDepartment of Biological Physics, Institute of Physics, Faculty of Science, Eötvös Loránd University, Budapest, Hungary.
Róbert HorváthNanobiosensorics "Lendület" Group, Institute of Technical Physics and Material Sciences, Centre for Energy Research, Hungarian Academy of Sciences, Budapest, Hungary.
Anna ErdeiMTA-ELTE Immunology Research Group, Hungarian Academy of Sciences, Budapest, Hungary.
Zsuzsa BajtayDepartment of Immunology, Institute of Biology, Faculty of Science, Eötvös Loránd University, Budapest, Hungary.
Eötvös Loránd University · HUNanobiosensorics Laboratory · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complement receptors CR3 (CD11b/CD18) and CR4 (CD11c/CD18) belong to the family of beta2 integrins and are expressed mainly by myeloid cell types in humans. Previously, we proved that CR3 rather than CR4 plays a key role in phagocytosis. Here we analysed how CD11b and CD11c participate in cell adhesion to fibrinogen, a common ligand of CR3 and CR4, employing human monocytes, monocyte-derived macrophages (MDMs) and monocyte-derived dendritic cells (MDDCs) highly expressing CD11b as well as CD11c. We determined the exact numbers of CD11b and CD11c on these cell types by a bead-based technique, and found that the ratio of CD11b/CD11c is 1.2 for MDDCs, 1.7 for MDMs and 7.1 for monocytes, suggesting that the function of CD11c is preponderant in MDDCs and less pronounced in monocytes. Applying state-of-the-art biophysical techniques, we proved that cellular adherence to fibrinogen is dominated by CD11c. Furthermore, we found that blocking CD11b significantly enhances the attachment of MDDCs and MDMs to fibrinogen, demonstrating a competition between CD11b and CD11c for this ligand. On the basis of the cell surface receptor numbers and the measured adhesion strength we set up a model, which explains the different behavior of the three cell types.

Identifiers

PMID27658051
PMCPMC5033469
OpenAlexW2522866345

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.