Acicular, but not globular, titanium dioxide nanoparticles stimulate keratinocytes to produce pro-inflammatory cytokines
Abstract
Titanium dioxide (TiO2 ) nanoparticles, widely used for daily products, are believed to be biologically inert, but they may cause adverse effects on cells, presumably depending on the particle size and shape. One of the critical targets of TiO2 particles is epidermal keratinocytes, and their initial response to TiO2 may be production of pro-inflammatory cytokines. We therefore investigated the effects of four types of TiO2 particles on cytokine expression/production by real-time reverse transcription polymerase chain reaction and enzyme-linked immunoassay. The TiO2 particles included three acicular types, FTL-100 (length, 1.68 μm; diameter, 130 nm), FTL-200 (2.86, 210) and FTL-300 (5.15, 270), and one globular type, PT-301 (diameter, 270 nm). Normal human epidermal keratinocytes (NHEK) were cultured with each of the TiO2 particles. During cultivation, the acicular forms of TiO2 were seen by scanning electron microscopy to be internalized by NHEK. The three acicular particles increased the mRNA expressions and supernatant productions of interleukin (IL)-1α, IL-1β, IL-6, tumor necrosis factor-α and IL-8 in particle number-dependent manners, whereas globular PT-301 had very weak activity. Thus, TiO2 particles may induce skin inflammation depending on the size and shape, providing knowledge on their health usage.
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Exposure to high concentrations of particulate matter with an average size <2.5 μm emitted by forest fires disrupts the epidermal barrier by damaging structural proteins (filaggrin and E-cadherin), and lipids in the epidermis.
“An example of environmental pressure that can determine alarmin secretion by keratinocytes in the epidermis is the exposure to high concentrations of particulate matter with an average size <2.5 µm emitted by forest fires, which disrupts the epidermal barrier by damaging structural proteins (filaggrin and E -cadherin), and lipids in the epidermis.”
From Update on the pathogenesis of atopic dermatitis. (2024) · cites this paper as [62]
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Filaggrin Mutations Associated with Skin and Allergic Diseases
Irvine, A. D., McLean, W. H. I., & Leung, D. Y. M. (2011) · New England Journal of Medicine · doi:10.1056/nejmra1011040 · Cited by 1,217 · see citing works
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Update on the pathogenesis of atopic dermatitis.
Criado, P. R., Miot, H. A., Bueno-Filho, R., Ianhez, M., Criado, R. F. J., & de Castro, C. C. S. (2024) · Anais brasileiros de dermatologia · doi:10.1016/j.abd.2024.06.001 · Cited by 66 · see citing works
Recent advancements in the atopic dermatitis mechanism
Savva, M., Papadopoulos, N. G., Gregoriou, S., Katsarou, S., Papapostolou, N., Makris, M., & Xepapadaki, P. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2902084 · Cited by 53 · see citing works
- Authors
- Hiroike, M., Sakabe, J., Kobayashi, M., Shimauchi, T., Ito, T., Hirakawa, S., Inoh, A., & Tokura, Y.
- Affiliations
- Hamamatsu University School of Medicine (JP)
- University of Occupational and Environmental Health Japan (JP)
- Nanbu Plastics Shizuoka Japan
- Corresponding author
- Tokura, Yoshiki
- Venue
- The Journal of Dermatology
- Publisher
- Wiley
- Published
- 2013-03-12
- Volume
- 40
- Issue
- 5
- Pages
- 357-362
- ISSN
- 0385-2407 (ISSN-L)
- 1346-8138
- OpenAlex
- W2035490625
- Cited by
- 16
- References
- 1
- Citations by year
- 2025: 1 · 2024: 4 · 2022: 3 · 2020: 1 · 2019: 2 · 2018: 1 · 2016: 1 · 2015: 2 · 2014: 1
- FWCI
- 0.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Dermatology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Nanoparticles: synthesis and applications
- Health Sciences › Medicine › Dermatology › Contact Dermatitis and Allergies
- Life Sciences › Immunology and Microbiology › Immunology › Immunotoxicology and immune responses
- Keywords
- titanium dioxide nanoparticles, acicular particles, globular particles, particle shape, particle size, keratinocytes, inflammatory cytokines, skin inflammation, interleukin-1, interleukin-6, TNF-α, interleukin-8, IL-1β, nanoparticle uptake
- MeSH terms
- Cells, Cultured, Humans, Titanium, Keratinocytes, Interleukin-8, Nanoparticles, Inflammasomes
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