Traffic-related PM2.5 induces cytosolic [Ca²⁺] increase regulated by Orai1, alters the CaN-NFAT signaling pathway, and affects IL-2 and TNF-α cytoplasmic levels in Jurkat T-cells

Arch Environ Contam Toxicol. 2015 Jan;68(1):31-7. doi: 10.1007/s00244-014-0077-8. Epub 2014 Sep 7.

Abstract

The atmospheric particulate matter with a diameter less than or equal to 2.5 um (PM2.5) can result in increased immune system damage or diseases, however, the possible mechanism remains unclear. In this study, we used Jurkat T cells to determine the effects of PM2.5 on T cell-mediated adaptive immune response. Our results indicated that PM2.5 exposure increased intracellular calcium ion concentration [Ca(2+)]. In contrast, cytosolic free Ca(2+) concentration [Ca(2+)]i significantly decreased in Jurkat T cells transfected with Orai1siRNA. In addition, we detected the level of interleukin (IL)-2 and tumor-necrosis factor (TNF)-α as well as other signalling molecules, including calcineurin (CaN) and NFATc2, a gene on 20q13.2 that encodes a member of the nuclear factor of activated T cells (NFAT), in the supernatant of cells exposed to PM2.5. The expression of NFATc2 protein increased in a time-dependent manner after exposure to PM2.5, but the activity of CaN decreased. NFATc2 was not consistent with IL-2 accumulation, thus indicating the involvement of other signals in the suppression of IL-2 accumulation. Our findings demonstrate that PM2.5 exposure in immune cells results in locally increased [Ca(2+)]i generated by Orai1 and CaN-NFAT gene expression, TNF-α and IL-2 cytoplasmic concentrations may be altered.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / metabolism*
  • Calcium Channels / metabolism*
  • Gene Expression
  • Gene Expression Regulation / drug effects*
  • Humans
  • Interleukin-2 / metabolism*
  • Jurkat Cells
  • NFATC Transcription Factors / metabolism
  • ORAI1 Protein
  • Particulate Matter / toxicity*
  • T-Lymphocytes
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Calcium Channels
  • Interleukin-2
  • NFATC Transcription Factors
  • ORAI1 Protein
  • ORAI1 protein, human
  • Particulate Matter
  • Tumor Necrosis Factor-alpha
  • Calcium