Activation of matrix metalloproteinases and FoxO3a in HaCaT keratinocytes by radiofrequency electromagnetic field exposure

2021 · Harm · Low evidence

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HarmLow evidencePaper 1175

Exposure to 1760 MHz RF-EMF (SAR 4.0 W/kg; 2 h/day for 4 days) increased intracellular ROS in HaCaT keratinocytes, increased MMP1/3/7 levels and increased gelatinolytic activity of secreted MMP2 and MMP9, and increased phosphorylation of FoxO3a and ERK1/2. Ce…

Study snapshot

Publicationmanual · 2021
Study typein_vitro
Reported directionHarm
Evidence ratingLow

Abstract

Activation of matrix metalloproteinases and FoxO3a in HaCaT keratinocytes by radiofrequency electromagnetic field exposure Ju Hwan Kim, Dong-Jun Kang, Jun-Sang Bae, Jai Hyuen Lee, Sangbong Jeon, Hyung-Do Choi, Nam Kim, Hyung- Gun Kim, Hak Rim Kim. Activation of matrix metalloproteinases and FoxO3a in HaCaT keratinocytes by radiofrequency electromagnetic field exposure. Sci Rep. 2021 Apr 7;11(1):7680. doi: 10.1038/s41598-021- 87263-2. Abstract As the skin is the largest body organ and critically serves as a barrier, it is frequently exposed and could be physiologically affected by radiofrequency electromagnetic field (RF-EMF) exposure. In this study, we found that 1760 MHz RF-EMF (4.0 W/kg specific absorption rate for 2 h/day during 4 days) exposure could induce intracellular reactive oxygen species (ROS) production in HaCaT human keratinocytes using 2',7'- dichlorofluorescin diacetate fluorescent probe analysis. However, cell growth and viability were unaffected by RF-EMF exposure. Since oxidative stress in the skin greatly influences the skin-aging process, we analyzed the skin senescence-related factors activated by ROS generation. Matrix metalloproteinases 1, 3, and 7 (MMP1, MMP3, and MMP7), the main skin wrinkle-related proteins, were significantly increased in HaCaT cells after RF- EMF exposure. Additionally, the gelatinolytic activities of secreted MMP2 and MMP9 were also increased by RF- EMF exposure. FoxO3a (Ser318/321) and ERK1/2 (Thr 202/Tyr 204) phosphorylation levels were significantly increased by RF-EMF exposure. However, Bcl2 and Bax expression levels were not significantly changed, indicating that the apoptotic pathway was not activated in keratinocytes following RF-EMF exposure. In summary, our findings show that exposure to 1760 MHz RF-EMF induces ROS generation, leading to MMP activation and FoxO3a and ERK1/2 phosphorylation. These data suggest that RF-EMF exposure induces cellular senescence of skin cells through ROS induction in HaCaT human keratinocytes. Conclusion In conclusion, exposure to 1760 MHz RF-EMF at 4 W/kg SAR induced intracellular ROS generation, which then stimulated MMPs (MMP1, 2, 3, 7, and 9) and activated the ERK1/2 (phospho-ERK1/2) and FoxO3a (phospho- FoxO3a) signaling pathways in HaCaT cells. Our results suggest that these changes induced by RF-EMF exposure would contribute to skin-aging processes. Open access paper: ncbi.nlm.nih.gov

Machine Enhanced Logic

AI evidence extraction

Structured fields below were generated from the paper’s abstract and metadata to make the evidence easier to inspect. Automated extraction may be incomplete or incorrect; verify important details against the original paper.

Study typein_vitro
Effect directionharm
PopulationHaCaT human keratinocytes
Sample sizeNot supplied
ExposureRF · 1760 MHz · 4 W/kg · 2 h/day during 4 days
Evidence strengthLowConfidence: 78% · Peer reviewed: yes

Main findings

Exposure to 1760 MHz RF-EMF (SAR 4.0 W/kg; 2 h/day for 4 days) increased intracellular ROS in HaCaT keratinocytes, increased MMP1/3/7 levels and increased gelatinolytic activity of secreted MMP2 and MMP9, and increased phosphorylation of FoxO3a and ERK1/2. Cell growth/viability were unaffected and Bcl2/Bax expression was not significantly changed.

Outcomes measured

  • Intracellular reactive oxygen species (ROS) production
  • Cell growth
  • Cell viability
  • MMP1, MMP3, MMP7 levels
  • Gelatinolytic activity of secreted MMP2 and MMP9
  • FoxO3a (Ser318/321) phosphorylation
  • ERK1/2 (Thr202/Tyr204) phosphorylation
  • Bcl2 expression
  • Bax expression
  • Apoptotic pathway activation
  • Cellular senescence/skin-aging related factors
View raw extracted JSON
{
  "study_type": "in_vitro",
  "exposure": {
    "band": "RF",
    "source": null,
    "frequency_mhz": 1760,
    "sar_wkg": 4,
    "duration": "2 h/day during 4 days"
  },
  "population": "HaCaT human keratinocytes",
  "sample_size": null,
  "outcomes": [
    "Intracellular reactive oxygen species (ROS) production",
    "Cell growth",
    "Cell viability",
    "MMP1, MMP3, MMP7 levels",
    "Gelatinolytic activity of secreted MMP2 and MMP9",
    "FoxO3a (Ser318/321) phosphorylation",
    "ERK1/2 (Thr202/Tyr204) phosphorylation",
    "Bcl2 expression",
    "Bax expression",
    "Apoptotic pathway activation",
    "Cellular senescence/skin-aging related factors"
  ],
  "main_findings": "Exposure to 1760 MHz RF-EMF (SAR 4.0 W/kg; 2 h/day for 4 days) increased intracellular ROS in HaCaT keratinocytes, increased MMP1/3/7 levels and increased gelatinolytic activity of secreted MMP2 and MMP9, and increased phosphorylation of FoxO3a and ERK1/2. Cell growth/viability were unaffected and Bcl2/Bax expression was not significantly changed.",
  "effect_direction": "harm",
  "limitations": [],
  "evidence_strength": "low",
  "confidence": 0.78,
  "peer_reviewed_likely": "yes",
  "keywords": [
    "RF-EMF",
    "1760 MHz",
    "specific absorption rate",
    "SAR",
    "HaCaT",
    "keratinocytes",
    "ROS",
    "oxidative stress",
    "matrix metalloproteinases",
    "MMP1",
    "MMP2",
    "MMP3",
    "MMP7",
    "MMP9",
    "FoxO3a",
    "ERK1/2",
    "skin aging",
    "cellular senescence"
  ],
  "suggested_hubs": []
}
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AI-extracted fields are generated from the abstract and metadata and may be incomplete or incorrect. This material is for informational purposes and is not medical advice.

Identifiers and source

DOI: 10.1038/s41598-021
PubMed: Not supplied

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