Evidence map›Paper›PMID 29348435›Full record

ArticleScientific reports2018

Macrophage sensing of single-walled carbon nanotubes via Toll-like receptors.

Sourav P Mukherjee, Olesja Bondarenko, Pekka Kohonen, Fernando T Andón, Táňa Brzicová, Isabel Gessner, Sanjay Mathur, Massimo Bottini, Paolo Calligari, Lorenzo Stella and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Understanding the immunological interactions of engineered nanomaterials: Role of the bio-corona.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2022
    Review
  7. Immunotoxicity of Carbon-Based Nanomaterials, Starring Phagocytes.International journal of molecular sciences · 2022
    Review
  8. Review
  9. A New Look at the Effects of Engineered ZnO and TiONanomaterials (Basel, Switzerland) · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Biocompatibility of nanomaterials and their immunological properties.Biomedical materials (Bristol, England) · 2021
    Review
  18. Article
  19. Article
  20. 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

16 authors at 8 institutions in 7 countries.

Sourav P MukherjeeNanosafety & Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden.
Olesja BondarenkoNanosafety & Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden.
Pekka KohonenNanosafety & Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-7845-3611
Fernando T AndónNanosafety & Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden.
Táňa BrzicováNanosafety & Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden.
Isabel GessnerInorganic and Materials Chemistry, University of Cologne, 50939, Cologne, Germany.
Sanjay MathurInorganic and Materials Chemistry, University of Cologne, 50939, Cologne, Germany.
Massimo BottiniDepartment of Experimental Medicine and Surgery, University of Rome Tor Vergata, Rome, 00173, Italy.
Paolo CalligariDepartment of Chemical Sciences and Technologies, University of Rome Tor Vergata, Rome, 00133, Italy.
Lorenzo StellaDepartment of Chemical Sciences and Technologies, University of Rome Tor Vergata, Rome, 00133, Italy.ORCID http://orcid.org/0000-0002-5489-7381
Elena KisinExposure Assessment Branch, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Anna ShvedovaExposure Assessment Branch, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.
Reija AutioFaculty of Social Sciences, University of Tampere, 33014, Tampere, Finland.
Heli Salminen-MankonenTurku Centre for Biotechnology, University of Turku, 20520 Turku, and Åbo Akademi University, 20500, Turku, Finland.
Riitta LahesmaaTurku Centre for Biotechnology, University of Turku, 20520 Turku, and Åbo Akademi University, 20500, Turku, Finland.
Bengt FadeelNanosafety & Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden. Bengt.Fadeel@ki.se.
Karolinska Institutet · SEUniversity of Rome Tor Vergata · ITÅbo Akademi University · FIUniversity of Cologne · DEHumanitas University · ITNational Institute for Occupational Safety and Health · USTampere University · FIWest Virginia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbon-based nanomaterials including carbon nanotubes (CNTs) have been shown to trigger inflammation. However, how these materials are 'sensed' by immune cells is not known. Here we compared the effects of two carbon-based nanomaterials, single-walled CNTs (SWCNTs) and graphene oxide (GO), on primary human monocyte-derived macrophages. Genome-wide transcriptomics assessment was performed at sub-cytotoxic doses. Pathway analysis of the microarray data revealed pronounced effects on chemokine-encoding genes in macrophages exposed to SWCNTs, but not in response to GO, and these results were validated by multiplex array-based cytokine and chemokine profiling. Conditioned medium from SWCNT-exposed cells acted as a chemoattractant for dendritic cells. Chemokine secretion was reduced upon inhibition of NF-κB, as predicted by upstream regulator analysis of the transcriptomics data, and Toll-like receptors (TLRs) and their adaptor molecule, MyD88 were shown to be important for CCL5 secretion. Moreover, a specific role for TLR2/4 was confirmed by using reporter cell lines. Computational studies to elucidate how SWCNTs may interact with TLR4 in the absence of a protein corona suggested that binding is guided mainly by hydrophobic interactions. Taken together, these results imply that CNTs may be 'sensed' as pathogens by immune cells.

Indexed as

Nanotubes, CarbonCells, CulturedChemokinesCytotoxicity, ImmunologicGene Expression ProfilingGene Regulatory NetworksHost-Pathogen InteractionsHumansHydrophobic and Hydrophilic InteractionsMacrophagesModels, MolecularMolecular ConformationReproducibility of ResultsSignal TransductionToll-Like ReceptorsTranscriptomeChemokinesNanotubes, CarbonToll-Like Receptors

Identifiers

PMID29348435
PMCPMC5773626
OpenAlexW2784042879

What OpenQuestion holds

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Registered trials

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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.