Evidence map›Paper›PMID 31787980›Full record

ArticleFrontiers in immunology2019

Zinc Oxide Nanowires Exposure Induces a Distinct Inflammatory Response via CCL11-Mediated Eosinophil Recruitment.

Ruqaih S Alghsham, Shuchismita R Satpathy, Sobha R Bodduluri, Bindu Hegde, Venkatakrishna R Jala, Waleed Twal, Joseph A Burlison, Mahendra Sunkara, Bodduluri Haribabu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. 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
1.1field-weighted citation impact, top 21% 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, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. AnThe Saudi dental journal · 2021
    Article
  8. Recent Advances in Zinc Oxide Nanostructures with Antimicrobial Activities.International journal of molecular sciences · 2020
    Review
  9. Review
  10. 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

9 authors at 3 institutions in 1 country.

Ruqaih S AlghshamDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.
Shuchismita R SatpathyDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.
Sobha R BodduluriDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.
Bindu HegdeDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.
Venkatakrishna R JalaDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.
Waleed TwalRegenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC, United States.
Joseph A BurlisonJames Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Mahendra SunkaraDepartment of Chemical Engineering, Conn Center for Renewable Energy, University of Louisville, Louisville, KY, United States.
Bodduluri HaribabuDepartment of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.
University of Louisville · USJames Graham Brown Foundation · USMedical University of South Carolina · US

Funding

Understanding the Host-Microbiome-Therapeutic Triad: Implications for Designing Alternative IntravaginalP20GM125504 · NIGMS · UNIVERSITY OF LOUISVILLE · PI James Tristan Collins · 2018 to 2026
$24.4M
Innate immune mechanisms regulating silicosisR21AI130756 · NIAID · UNIVERSITY OF LOUISVILLE · PI BODDULURI, HARIBABU · 2017 to 2018
$424k
NIAID NIH HHS R21 AI130756NIGMS NIH HHS P20 GM125504
6 · The paper itself

Abstract

High aspect ratio zinc oxide nanowires (ZnONWs) have become one of the most important products in nanotechnology. The wide range applications of ZnONWs have heightened the need for evaluating the risks and biological consequences to these particles. In this study, we investigated inflammatory pathways activated by ZnONWs in cultured cells as well as the consequences of systemic exposure in mouse models. Confocal microscopy showed rapid phagocytic uptake of FITC-ZnONWs by macrophages. Exposure of macrophages or lung epithelial cells to ZnONWs induced the production of CCL2 and CCL11. Moreover, ZnONWs exposure induced both IL-6 and TNF-α production only in macrophages but not in LKR13 cells. Intratracheal instillation of ZnONWs in C57BL/6 mice induced a significant increase in the total numbers of immune cells in the broncho alveolar lavage fluid (BALFs) 2 days after instillation. Macrophages and eosinophils were the predominant cellular infiltrates of ZnONWs exposed mouse lungs. Similar cellular infiltrates were also observed in a mouse air-pouch model. Pro-inflammatory cytokines IL-6 and TNF-α as well as chemokines CCL11, and CCL2 were increased both in BALFs and air-pouch lavage fluids. These results suggest that exposure to ZnONWs may induce distinct inflammatory responses through phagocytic uptake and formation of soluble Zn

Indexed as

AnimalsChemokine CCL11Chemokine CCL2Disease Models, AnimalEosinophilsInflammationInflammation MediatorsInterleukin-6In Vitro TechniquesMacrophagesMiceMice, Inbred C57BLNanowiresNeutrophilsRAW 264.7 CellsRNA, MessengerCcl11 protein, mouseCcl2 protein, mouseChemokine CCL11Chemokine CCL2Inflammation MediatorsInterleukin-6interleukin-6, mouseRNA, MessengerTumor Necrosis Factor-alphaZinc Oxideengineered nanomaterialslung inflammationmurine modeltoxicityzinc oxide nanoparticleszinc oxide nanowires

Identifiers

PMID31787980
PMCPMC6856074
OpenAlexW2981761028

What OpenQuestion holds

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LicenceCC BY
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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.