Evidence map›Paper›PMID 34864742›Full record

ArticleJournal of innate immunity2022

Broad Ultrastructural and Transcriptomic Changes Underlie the Multinucleated Giant Hemocyte Mediated Innate Immune Response against Parasitoids.

Gyöngyi Cinege, Lilla B Magyar, Attila L Kovács, Zita Lerner, Gábor Juhász, David Lukacsovich, Jochen Winterer, Tamás Lukacsovich, Zoltán Hegedűs, Éva Kurucz and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of innate immunity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Germline and Somatic Cell Syncytia in Insects.Results and problems in cell differentiation · 2024
    Review
  7. Distinctive features ofFrontiers in immunology · 2023
    Article
  8. 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

13 authors at 5 institutions in 3 countries.

Gyöngyi CinegeInstitute of Genetics, Innate Immunity Group, Immunology Unit, Biological Research Centre, Szeged, Hungary.
Lilla B MagyarInstitute of Genetics, Innate Immunity Group, Immunology Unit, Biological Research Centre, Szeged, Hungary.
Attila L KovácsDepartment of Anatomy, Cell and Developmental Biology, Eötvös Loránd University, Budapest, Hungary.
Zita LernerInstitute of Genetics, Innate Immunity Group, Immunology Unit, Biological Research Centre, Szeged, Hungary.
Gábor JuhászDepartment of Anatomy, Cell and Developmental Biology, Eötvös Loránd University, Budapest, Hungary.
David LukacsovichLaboratory of Neural Connectivity, Brain Research Institute, University of Zurich, Zurich, Switzerland.
Jochen WintererLaboratory of Neural Connectivity, Brain Research Institute, University of Zurich, Zurich, Switzerland.
Tamás LukacsovichLaboratory of Neural Connectivity, Brain Research Institute, University of Zurich, Zurich, Switzerland.
Zoltán HegedűsLaboratory of Bioinformatics, Biological Research Centre, Szeged, Hungary.
Éva KuruczInstitute of Genetics, Innate Immunity Group, Immunology Unit, Biological Research Centre, Szeged, Hungary.
Dan HultmarkDepartment of Molecular Biology, Umea University, Umea, Sweden.
Csaba FöldyLaboratory of Neural Connectivity, Brain Research Institute, University of Zurich, Zurich, Switzerland.
István AndóInstitute of Genetics, Innate Immunity Group, Immunology Unit, Biological Research Centre, Szeged, Hungary.
HUN-REN Szegedi Biológiai Kutatóközpont · HUUniversity of Zurich · CHEötvös Loránd University · HUUniversity of Szeged · HUUmeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multinucleated giant hemocytes (MGHs) represent a novel type of blood cell in insects that participate in a highly efficient immune response against parasitoid wasps involving isolation and killing of the parasite. Previously, we showed that circulating MGHs have high motility and the interaction with the parasitoid rapidly triggers encapsulation. However, structural and molecular mechanisms behind these processes remained elusive. Here, we used detailed ultrastructural analysis and live cell imaging of MGHs to study encapsulation in Drosophila ananassae after parasitoid wasp infection. We found dynamic structural changes, mainly driven by the formation of diverse vesicular systems and newly developed complex intracytoplasmic membrane structures, and abundant generation of giant cell exosomes in MGHs. In addition, we used RNA sequencing to study the transcriptomic profile of MGHs and activated plasmatocytes 72 h after infection, as well as the uninduced blood cells. This revealed that differentiation of MGHs was accompanied by broad changes in gene expression. Consistent with the observed structural changes, transcripts related to vesicular function, cytoskeletal organization, and adhesion were enriched in MGHs. In addition, several orphan genes encoding for hemolysin-like proteins, pore-forming toxins of prokaryotic origin, were expressed at high level, which may be important for parasitoid elimination. Our results reveal coordinated molecular and structural changes in the course of MGH differentiation and parasitoid encapsulation, providing a mechanistic model for a powerful innate immune response.

Indexed as

HemocytesWaspsAnimalsDrosophilaHost-Parasite InteractionsImmunity, InnateTranscriptomeDrosophilaEncapsulationInnate immunityMultinucleated giant hemocyteTranscriptome

Identifiers

PMID34864742
PMCPMC9275024
OpenAlexW4200116665

What OpenQuestion holds

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LicenceCC BY-NC
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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.