Evidence map›Paper›PMID 31553970›Full record

ArticleJournal of innate immunity2020

Cellular Immune Response Involving Multinucleated Giant Hemocytes with Two-Step Genome Amplification in the Drosophilid Zaprionus indianus.

Gyöngyi Cinege, Zita Lerner, Lilla B Magyar, Bálint Soós, Renáta Tóth, Ildikó Kristó, Péter Vilmos, Gábor Juhász, Attila L Kovács, Zoltán Hegedűs and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of innate immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Germline and Somatic Cell Syncytia in Insects.Results and problems in cell differentiation · 2024
    Review
  6. Distinctive features ofFrontiers in immunology · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Once upon a Time.Journal of innate immunity · 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

13 authors at 6 institutions in 2 countries.

Gyöngyi CinegeImmunology Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Zita LernerImmunology Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Lilla B MagyarImmunology Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Bálint SoósImmunology Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Renáta TóthImmunology Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Ildikó KristóDevelopmental Genetics Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Péter VilmosDevelopmental Genetics Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Gábor JuhászDepartment of Anatomy, Cell and Developmental Biology, Eötvös Loránd University, Budapest, Hungary.
Attila L KovácsDepartment of Anatomy, Cell and Developmental Biology, Eötvös Loránd University, Budapest, Hungary.
Zoltán HegedűsLaboratory of Bioinformatics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Christoph W SensenInstitute of Computational Biotechnology, Graz University of Technology, Graz, Austria.
Éva KuruczImmunology Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
István AndóImmunology Unit, Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary, ando@brc.hu.
Hungarian Academy of Sciences · HUInstitute of Genetics · HUEötvös Loránd University · HUHUN-REN Szegedi Biológiai Kutatóközpont · HUGraz University of Technology · ATUniversity of Szeged · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously, a novel cell type, the multinucleated giant hemocyte (MGH) was identified in the ananassae subgroup of Drosophilidae. These cells share several features with mammalian multinucleated giant cells, a syncytium of macrophages formed during granulomatous inflammation. We were able to show that MGHs also differentiate in Zaprionus indianus, an invasive species belonging to the vittiger subgroup of the family, highly resistant to a large number of parasitoid wasp species. We have classified the MGHs of Z. indianusas giant hemocytes belonging to a class of cells which also include elongated blood cells carrying a single nucleus and anuclear structures. They are involved in encapsulating parasites, originate from the lymph gland, can develop by cell fusion, and generally carry many nuclei, while possessing an elaborated system of canals and sinuses, resulting in a spongiform appearance. Their nuclei are all transcriptionally active and show accretion of genetic material. Multinucleation and accumulation of the genetic material in the giant hemocytes represents a two-stage amplification of the genome, while their spongy ultrastructure substantially increases the contact surface with the extracellular space. These features may furnish the giant hemocytes with a considerable metabolic advantage, hence contributing to the mechanism of the effective immune response.

Indexed as

Genome, InsectImmunity, CellularAnimalsDrosophilidaeGiant CellsHemocytesDrosophilaEncapsulationGranulomaHemocyteHost defenseImmunityMultinucleatedParasitologyZaprionus indianus

Identifiers

PMID31553970
PMCPMC7265743
OpenAlexW2974965060

What OpenQuestion holds

Textmetadata
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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.