Effects of Ambient Fine Particles PM2.5 on Human HaCaT Cells

Int J Environ Res Public Health. 2017 Jan 12;14(1):72. doi: 10.3390/ijerph14010072.

Abstract

The current study was conducted to observe the effects of fine particulate matter (PM2.5) on human keratinocyte cell line (HaCaT) cells. The potential mechanism linking PM2.5 and skin was explored. HaCaT cells were cultured and then accessed in plate with PM2.5. Cell viability was tested by Cell Counting Kit-8. The mRNA and protein expression of Filaggrin, Loricrin, Involucrin, and Repetin were analyzed. The levels of Granulocyte-macrophage Colony Stimulating Factor, Thymic Stromal Lymphopoietin, Tumor Necrosis Factor-α, Interleukin-1α, and Interleukin-8 were detected in the supernatant of the HaCaT cell with enzyme-linked immunosorbent assay kits. Cell viability decreased with the increase in PM2.5. Compared with the control group, the protein expression of Filaggrin, Repetin, Involucrin, and Loricrin showed different expression patterns in PM2.5 treatment groups. The level of Tumor Necrosis Factor-α, Thymic Stromal Lymphopoietin, Interleukin-1α, and Interleukin-8 significantly increased in the cells treated with PM2.5. Ambient PM2.5 may increase the risk of eczema and other skin diseases. The relative mechanism may be associated with the impairment of the skin barrier and the elevation of inflammatory responses.

Keywords: HaCaT cell; PM2.5; skin damage.

MeSH terms

  • Cell Line
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cytokines / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Filaggrin Proteins
  • Granulocyte-Macrophage Colony-Stimulating Factor / drug effects
  • Humans
  • Interleukin-1alpha / metabolism
  • Interleukin-8 / metabolism
  • Keratinocytes / drug effects*
  • Particulate Matter / pharmacology*
  • Protein Precursors
  • Skin / drug effects*
  • Skin / metabolism
  • Thymic Stromal Lymphopoietin
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • FLG protein, human
  • Filaggrin Proteins
  • Interleukin-1alpha
  • Interleukin-8
  • Particulate Matter
  • Protein Precursors
  • Tumor Necrosis Factor-alpha
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Thymic Stromal Lymphopoietin