Particulate matter induces pro-inflammatory cytokines via phosphorylation of p38 MAPK possibly leading to dermal inflammaging

Exp Dermatol. 2019 Jul;28(7):809-815. doi: 10.1111/exd.13943. Epub 2019 May 15.

Abstract

Particulate matter (PM) is known to have harmful effects on human health. Epidemiological studies have suggested that PM exposure is related to skin diseases and extrinsic skin ageing. However, the mechanisms by which PM affects skin are unclear. The aim of this study was to investigate the mechanism of action of PMs on epidermal inflammation and skin ageing using a co-culture of human keratinocytes (HaCaT) and fibroblasts (HDF). SRM 1648a (pmA) and 1649b (pmB), which mainly comprise heavy metals and polycyclic aromatic hydrocarbons, respectively, were used as reference PMs. Cytotoxic effects, activation of AhR, phosphorylation of p38 kinase and ROS generation were examined in PM-treated HaCaT cells. The phosphorylation of p38 MAPK induced by PMs was shown to be critically important for the increases in IL-1α and IL-1β expression. Moreover, the mRNA and protein expression levels of MMP1 and COX2 were markedly increased in HDF cells co-cultured with PM-treated HaCaT cells. In conclusion, PMs induce the expression of pro-inflammatory cytokines in keratinocytes via the p38 MAPK pathway, and these interleukins increase the expression of MMP1 and COX2 in HDF cells. These results suggest that PMs trigger skin ageing via p38 MAPK activation and interleukin secretion in epidermal keratinocytes.

Keywords: co-culture; interleukin-1; p38; particulate matter; skin ageing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival
  • Coculture Techniques
  • Collagen / metabolism
  • Cyclooxygenase 2 / metabolism
  • Cytokines / metabolism
  • Fibroblasts / metabolism
  • Humans
  • Inflammation / metabolism*
  • Interleukin-1alpha / metabolism
  • Interleukin-1beta / metabolism
  • Keratinocytes / cytology
  • Keratinocytes / metabolism
  • Matrix Metalloproteinase 1 / metabolism
  • Particulate Matter / pharmacology*
  • Phosphorylation / drug effects*
  • Reactive Oxygen Species / metabolism
  • Skin / metabolism
  • Skin Aging
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Cytokines
  • IL1A protein, human
  • IL1B protein, human
  • Interleukin-1alpha
  • Interleukin-1beta
  • Particulate Matter
  • Reactive Oxygen Species
  • Collagen
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • p38 Mitogen-Activated Protein Kinases
  • MMP1 protein, human
  • Matrix Metalloproteinase 1