Evidence map›Paper›PMID 29192209›Full record

ArticleScientific reports2017

Mineral particles stimulate innate immunity through neutrophil extracellular traps containing HMGB1.

Hsin-Hsin Peng, Yu-Ju Liu, David M Ojcius, Chiou-Mei Lee, Ren-Hao Chen, Pei-Rong Huang, Jan Martel, John D Young

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
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

40 citing papers in PubMed.

  1. Article
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Targeting HMGB1: A Potential Therapeutic Strategy for Chronic Kidney Disease.International journal of biological sciences · 2023
    Review
  14. Article
  15. Activation of Neutrophils by Mucin-Vaterite Microparticles.International journal of molecular sciences · 2022
    Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. The mechanism of HMGB1 secretion and release.Experimental & molecular medicine · 2022
    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.

Hsin-Hsin PengLaboratory of Nanomaterials, Chang Gung University, Gueishan, Taoyuan, 33302, Taiwan.
Yu-Ju LiuLaboratory of Nanomaterials, Chang Gung University, Gueishan, Taoyuan, 33302, Taiwan.
David M OjciusCenter for Molecular and Clinical Immunology, Chang Gung University, Gueishan, Taoyuan, 33302, Taiwan.
Chiou-Mei LeeLaboratory Animal Center, Chang Gung Memorial Hospital, Gueishan, Taoyuan, 33305, Taiwan.
Ren-Hao ChenDepartment of Medical Research and Development, Chang Gung Memorial Hospital, Gueishan, Taoyuan, 33305, Taiwan.
Pei-Rong HuangLaboratory of Nanomaterials, Chang Gung University, Gueishan, Taoyuan, 33302, Taiwan.
Jan MartelLaboratory of Nanomaterials, Chang Gung University, Gueishan, Taoyuan, 33302, Taiwan.
John D YoungLaboratory of Nanomaterials, Chang Gung University, Gueishan, Taoyuan, 33302, Taiwan. jdyoung@mail.cgu.edu.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcium phosphate-based mineralo-organic particles form spontaneously in the body and may represent precursors of ectopic calcification. We have shown earlier that these particles induce activation of caspase-1 and secretion of IL-1β by macrophages. However, whether the particles may produce other effects on immune cells is unclear. Here, we show that these particles induce the release of neutrophil extracellular traps (NETs) in a size-dependent manner by human neutrophils. Intracellular production of reactive oxygen species is required for particle-induced NET release by neutrophils. NETs contain the high-mobility group protein B1 (HMGB1), a DNA-binding protein capable of inducing secretion of TNF-α by a monocyte/macrophage cell line and primary macrophages. HMGB1 functions as a ligand of Toll-like receptors 2 and 4 on macrophages, leading to activation of the MyD88 pathway and TNF-α production. Furthermore, HMGB1 is critical to activate the particle-induced pro-inflammatory cascade in the peritoneum of mice. These results indicate that mineral particles promote pro-inflammatory responses by engaging neutrophils and macrophages via signaling of danger signals through NETs.

Indexed as

Immunity, InnateImmunomodulationAnimalsCell LineExtracellular TrapsFemaleHMGB1 ProteinHumansMacrophage ActivationMacrophagesMaleMiceMineralsModels, MolecularMyeloid Differentiation Factor 88NeutrophilsHMGB1 ProteinMineralsMyeloid Differentiation Factor 88Reactive Oxygen SpeciesToll-Like Receptor 2Toll-Like Receptor 4Tumor Necrosis Factor-alpha

Identifiers

PMID29192209
PMCPMC5709501

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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.