Cited by 41Air Quality and Health ImpactsHeavy Metal Exposure and ToxicityIron Metabolism and Disorders

Wood Smoke Particle Sequesters Cell Iron to Impact a Biological Effect

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Ghio, Andrew J., Soukup, Joleen M., Dailey, Lisa A., Tong, Haiyan, Kesic, Matthew J., Budinger, G. R. Scott, Mutlu, Gökhan M.·2015·Chemical Research in Toxicology

Abstract

The biological effect of an inorganic particle (i.e., silica) can be associated with a disruption in cell iron homeostasis. Organic compounds included in particles originating from combustion processes can also complex sources of host cell iron to disrupt metal homeostasis. We tested the postulate that (1) wood smoke particle (WSP) sequesters host cell iron resulting in a disruption of metal homeostasis, (2) this loss of essential metal results in both an oxidative stress and biological effect in respiratory epithelial cells, and (3) humic-like substances (HULIS), a component of WSP, have a capacity to appropriate cell iron and initiate a biological effect. BEAS-2B cells exposed to WSP resulted in diminished concentrations of mitochondrial (57)Fe, whereas preincubation with ferric ammonium citrate (FAC) prevented significant mitochondrial iron loss after such exposure. Cellular oxidant generation was increased after WSP exposure, but this signal was diminished by coincubation with FAC. Similarly, exposure of BEAS-2B cells to 100 μg/mL WSP activated mitogen-activated protein (MAP) kinases, elevated NF-E2-related factor 2/antioxidant responsive element (Nrf2 ARE) expression, and provoked interleukin (IL)-6 and IL-8 release, but all these changes were diminished by coincubation with FAC. The biological response to WSP was reproduced by exposure to 100 μg/mL humic acid, a polyphenol comparable to HULIS included in the WSP that complexes iron. We conclude that (1) the biological response following exposure to WSP is associated with sequestration of cell iron by the particle, (2) increasing available iron in the cell diminished the biological effects after particle exposure, and (3) HULIS included in WSP can sequester the metal initiating the cell response.

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  • Cell exposure to asbestos activates mitogen-activated protein (MAP) kinases, and a portion of this response can be diminished by increasing the concentration of available iron.

    “Cell exposure to asbestos activates mitogen-activated protein (MAP) kinases, and a portion of this response can be diminished by increasing the concentration of available iron [52,53,54].”

    From Asbestos and Iron (2023) · cites this paper as [54]

    The Results and Discussion report that wood smoke particles activated MAP kinases in respiratory epithelial cells and that increasing available iron diminished the response. The cited paper tests wood smoke particles, not asbestos, so it does not establish the claim for asbestos exposure (page numbers unavailable in our copy). (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Increased iron availability decreases the activation of transcription factors following exposure to particles/fibers.

    “Comparable to MAP kinases, increased iron availability decreases the activation of transcription factors following exposure to particles/fibers [53,54,63].”

    From Asbestos and Iron (2023) · cites this paper as [54]

    The Results report that iron pretreatment diminished Nrf2 activation in BEAS-2B cells exposed to wood smoke particles. The claim extends that finding to transcription factors generally and to fiber exposure, neither of which is shown in the cited passages. (LLM, conf=0.84)

    Experimental — accuracy not yet measured

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References 49 · Cited by 41

Research works printed but not linked: 1

  1. [13]Sporn TA Roggli VL 2008 Pneumoconioses, Mineral and Vegetable Dail and Hammar’s Pulmonary Pathology. Vol. I. Nonneoplastic Lung Disease Tomashefski JFJ Cagle PT Farver CF Fraire AE 933 Springer

Authors
Ghio, A. J., Soukup, J. M., Dailey, L. A., Tong, H., Kesic, M. J., Budinger, G. R. S., & Mutlu, G. M.
Affiliations
  • Environmental Protection Agency (US)
  • Methodist University (US)
  • Northwestern University (US)
  • Section of Pulmonary and Critical Care and Lung Injury Center, Department of Medicine, Chicago, Illinois 60637, United States
Corresponding author
Ghio, Andrew J.
Venue
Chemical Research in Toxicology
Published
2015-10-22
Volume
28
Issue
11
Pages
2104-2111
ISSN
  • 0893-228X (ISSN-L)
  • 1520-5010
OpenAlex
W2312223701
Cited by
41
References
49
Citations by year
2026: 1 · 2025: 3 · 2024: 2 · 2023: 4 · 2022: 3 · 2021: 6 · 2020: 5 · 2019: 5 · 2018: 5 · 2017: 4 · 2016: 3
FWCI
2.51
Type
journal article
Language
en
Open access
Locations
  • Chemical Research in Toxicology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
U.S. Environmental Protection Agency
Topics
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Air Quality and Health Impacts
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Heavy Metal Exposure and Toxicity
  • Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
Keywords
iron sequestration, humic-like substances, humic acid, mitochondrial iron, oxidative stress, airway epithelial cells, BEAS-2B cells, Nrf2, MAPK activation, interleukin-6, interleukin-8, ferric ammonium citrate, combustion particles, polyphenols
MeSH terms
Cell Line, Cell Nucleus, Humans, Humic Substances, Iron, Mitochondria, Smoke, Transcription Factors, Wood, Interleukin-6, Interleukin-8, Mitogen-Activated Protein Kinases

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