Evidence map›Paper›PMID 26744177›Full record

ArticleScientific reports2016

Sertoli cells have a functional NALP3 inflammasome that can modulate autophagy and cytokine production.

Soren Hayrabedyan, Krassimira Todorova, Asma Jabeen, Gergana Metodieva, Stavri Toshkov, Metodi V Metodiev, Milcho Mincheff, Nelson Fernández

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
1.7field-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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Exploring dysregulated miRNAs in cryptorchidism: a systematic review.The Journal of international medical research · 2021
    Pooled it
  2. Guideline
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Cornelian Cherry (Biology · 2025
    Article
  9. Article
  10. Testicular immunity.Molecular aspects of medicine · 2024
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. 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 3 institutions in 2 countries.

Soren HayrabedyanInstitute of Biology and Immunology of Reproduction, Laboratory of Reproductive Omics Technologies, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Krassimira TodorovaInstitute of Biology and Immunology of Reproduction, Laboratory of Reproductive Omics Technologies, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Asma JabeenSchool of Biological Sciences, Wivenhoe Park, University of Essex, Colchester, UK.
Gergana MetodievaSchool of Biological Sciences, Wivenhoe Park, University of Essex, Colchester, UK.
Stavri ToshkovCellular and Gene Therapy Ward, National Specialized Haematology Hospital, Sofia, Bulgaria.
Metodi V MetodievSchool of Biological Sciences, Wivenhoe Park, University of Essex, Colchester, UK.
Milcho MincheffCellular and Gene Therapy Ward, National Specialized Haematology Hospital, Sofia, Bulgaria.
Nelson FernándezSchool of Biological Sciences, Wivenhoe Park, University of Essex, Colchester, UK.
University of Essex · GBInstitute of Biology and Immunology of Reproduction · BGNational Specialized Hospital for Active Treatment of Hematologic Diseases · BG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sertoli cells, can function as non-professional tolerogenic antigen-presenting cells, and sustain the blood-testis barrier formed by their tight junctions. The NOD-like receptor family members and the NALP3 inflammasome play a key role in pro-inflammatory innate immunity signalling pathways. Limited data exist on NOD1 and NOD2 expression in human and mouse Sertoli cells. Currently, there is no data on inflammasome expression or function in Sertoli cells. We found that in primary pre-pubertal Sertoli cells and in adult Sertoli line, TLR4\NOD1 and NOD2 crosstalk converged in NFκB activation and elicited a NALP3 activation, leading to de novo synthesis and inflammasome priming. This led to caspase-1 activation and IL-1β secretion. We demonstrated this process was controlled by mechanisms linked to autophagy. NOD1 promoted pro-IL-1β restriction and autophagosome maturation arrest, while NOD2 promoted caspase-1 activation, IL-1β secretion and autophagy maturation. NALP3 modulated NOD1 and pro-IL-1β expression, while NOD2 inversely promoted IL-1β. This study is proof of concept that Sertoli cells, upon specific stimulation, could participate in male infertility pathogenesis via inflammatory cytokine induction.

Indexed as

AnimalsAntigen-Presenting CellsAutophagyBlood-Testis BarrierCaspase 1Gene Expression RegulationImmunity, InnateInflammasomesInterleukin-1betaMaleMiceMice, Inbred BALB CNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNod1 Signaling Adaptor ProteinNod2 Signaling Adaptor ProteinCaspase 1IL1B protein, mouseInflammasomesInterleukin-1betaNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseNod1 protein, mouseNod1 Signaling Adaptor ProteinNod2 protein, mouseNod2 Signaling Adaptor ProteinTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID26744177
PMCPMC4705529
OpenAlexW2297987452

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.