Evidence map›Paper›PMID 31853340›Full record

ArticleJournal of extracellular vesicles2020

Role of Mac-1 integrin in generation of extracellular vesicles with antibacterial capacity from neutrophilic granulocytes.

Ákos M Lőrincz, Balázs Bartos, Dávid Szombath, Viktória Szeifert, Csaba I Timár, Lilla Turiák, László Drahos, Ágnes Kittel, Dániel S Veres, Ferenc Kolonics and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Extracellular Vesicles from Immune Cells: A Biomedical Perspective.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
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  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Integrin Regulation in Immunological and Cancerous Cells and Exosomes.International journal of molecular sciences · 2021
    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

12 authors at 2 institutions in 1 country.

Ákos M LőrinczDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Balázs BartosDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Dávid SzombathDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Viktória SzeifertDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Csaba I TimárDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Lilla TuriákMS Proteomics Research Group, Research Centre for Natural Science, Hungarian Academy of Sciences, Budapest, Hungary.
László DrahosMS Proteomics Research Group, Research Centre for Natural Science, Hungarian Academy of Sciences, Budapest, Hungary.
Ágnes KittelExperimental Research Institute of Hungarian Academy of Sciences, Budapest, Hungary.
Dániel S VeresDepartment of Biophysics and Radiation Biology, Semmelweis University, Budapest, Hungary.
Ferenc KolonicsDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Attila MócsaiDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Erzsébet LigetiDepartment of Physiology, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUHungarian Academy of Sciences · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Production of extracellular vesicles (EVs) involved in intercellular communication is a common capacity of most cell types. Upon encountering opsonized microorganisms, neutrophilic granulocytes release EVs that compromise bacterial growth. We carried out a systematic investigation of the involvement of potential opsonin receptors in EV-generation from human and murine neutrophils. Applying flow cytometric, proteomic and functional analysis as well as using genetically modified mice, we demonstrate that formation of antibacterial EVs depends upon stimulation of the multifunctional Mac-1 integrin complex, also called as complement receptor 3 (CR3), whereas activation of immunoglobulin binding Fc receptors or pattern recognition receptors alone or in combination is ineffective. Mac-1/CR3 stimulation and downstream tyrosine kinase signalling affect both the numbers, the cargo content and the antibacterial capacity of the produced vesicles. In contrast, Mac-1/CR3 signalling is not required for spontaneous EV formation, clearly indicating the existence of separate molecular pathways in EV biogenesis. We propose that EVs are "tailor-made" with different composition and functional properties depending on the environmental circumstances.

Indexed as

bacterial growthcomplement receptorEV biogenesisextracellular vesiclesFc receptorinflammationMac-1 integrinNeutrophilsopsoninstyrosine kinase inhibitor

Identifiers

PMID31853340
PMCPMC6913618
OpenAlexW2996177743

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.