Evidence map›Paper›PMID 32434939›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2020

Thermal Burn Injury Generates Bioactive Microvesicles: Evidence for a Novel Transport Mechanism for the Lipid Mediator Platelet-Activating Factor (PAF) That Involves Subcellular Particles and the PAF Receptor.

Langni Liu, Katherine E Fahy, Azeezat A Awoyemi, Pariksha Thapa, Lisa E Kelly, Jay Chen, Ji C Bihl, David R Cool, Yanfang Chen, Christine M Rapp and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Intoxicated thermal burn injury-mediated systemic immunosuppression involves platelet-activating factor and microvesicle particles.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Article
  6. Article
  7. Radiation therapy produces microvesicle particle release in HaCaT keratinocytes.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2023
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Evidence for microvesicle particles in UVB-mediated IL-8 generation in keratinocytes.Journal of clinical and investigative dermatology · 2021
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

12 authors at 1 institution in 1 country.

Langni LiuDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.
Katherine E FahyDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.
Azeezat A AwoyemiDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.ORCID 0000-0002-0312-7635
Pariksha ThapaDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.ORCID 0000-0002-7368-2589
Lisa E KellyDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.
Jay ChenDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.
Ji C BihlDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.ORCID 0000-0003-2404-1782
David R CoolDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.
Yanfang ChenDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.
Christine M RappDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435.
R Michael JohnsonDepartment of Plastic Surgery, Wright State University, Dayton, OH 45435.ORCID 0000-0003-4358-5056
Jeffrey B TraversDepartment of Pharmacology and Toxicology, Wright State University, Dayton, OH 45435; jeffrey.travers@wright.edu.ORCID 0000-0001-7232-1039
Wright State University · US

Funding

Platelet Activating Factor and Epidermic CytotoxicityR01HL062996 · NHLBI · WRIGHT STATE UNIVERSITY · PI TRAVERS, JEFFREY B. · 1999 to 2023
$7.2M
UVB radiation-generated microvesicle particles as effectors for photosensitivityR01ES031087 · NIEHS · WRIGHT STATE UNIVERSITY · PI KEMP, MICHAEL GEORGE, TRAVERS, JEFFREY B. · 2021 to 2025
$1.7M
Microvesicles as a Novel Transmitter for UVB-Induced Bioactive ProductsR21AR071110 · NIAMS · WRIGHT STATE UNIVERSITY · PI BIHL, JI CHEN · 2017 to 2018
$358k
Oxidized Lipids and UV ImmunosuppressionI01BX000853 · VA · RLR VA MEDICAL CENTER · PI Jeffrey B. Travers · 2011 to 2026
–
BLRD VA I01 BX000853NHLBI NIH HHS R01 HL062996NIAMS NIH HHS R21 AR071110NIEHS NIH HHS R01 ES031087
6 · The paper itself

Abstract

Thermal burn injuries are an important environmental stressor that can result in considerable morbidity and mortality. The exact mechanism by which an environmental stimulus to skin results in local and systemic effects is an area of active research. One potential mechanism to allow skin keratinocytes to disperse bioactive substances is via microvesicle particles, which are subcellular bodies released directly from cellular membranes. Our previous studies have indicated that thermal burn injury of the skin keratinocyte in vitro results in the production of the lipid mediator platelet-activating factor (PAF). The present studies demonstrate that thermal burn injury to keratinocytes in vitro and human skin explants ex vivo, and mice in vivo generate microvesicle particles. Use of pharmacologic and genetic tools indicates that the optimal release of microvesicles is dependent upon the PAF receptor. Of note, burn injury-stimulated microvesicle particles do not carry appreciable protein cytokines yet contain high levels of PAF. These studies describe a novel mechanism involving microvesicle particles by which a metabolically labile bioactive lipid can travel from cells in response to environmental stimuli.

Indexed as

AnimalsBiopsyBurnsCell-Derived MicroparticlesCell LineDisease Models, AnimalFemaleHumansKeratinocytesLipid MetabolismMiceMice, KnockoutPlatelet Activating FactorPlatelet Membrane GlycoproteinsPrimary Cell CultureReceptors, G-Protein-CoupledPlatelet Activating Factorplatelet activating factor receptorPlatelet Membrane GlycoproteinsReceptors, G-Protein-Coupled

Identifiers

PMID32434939
PMCPMC7342023
OpenAlexW3027758700

What OpenQuestion holds

Textmetadata
LicenceTDM
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.