Pulmonary glass particles may persist in the lung suppressing function of immune cells

Eun Jung Park, Gwang Hee Lee, Jae Chan Kim, Sang Jin Lee, Kyuhong Lee, Byoung Seok Lee, Jaerak Chang, Dong-Wan Kim

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

The health effects of silica may depend on the inherent properties of crystalline silica or on external factors affecting the biological activity or distribution of its polymorphs. Inhaled crystalline silica is classified as a Group I carcinogen, however, information on the health effects of amorphous silica is still insufficient. Considering that alveolar macrophages play a key role in both innate and adaptive immune responses for removal of foreign bodies that enter via the respiratory system, we treated sheet-like glass particles (SGPs), a type of noncrystalline amorphous silica, to MH-S cells, an alveolar macrophage cell line. SGPs reduced the generation of ROS and NO and induced cell death via multiple pathways. Although the expression of CD80, CD86, and CD40, increased by exposure to SGPs, the expression of MHC class II molecules had not notably changed. Additionally, expression of ICAM-1 tended to decrease. In mice, SGPs were distributed in the interstitial region of the lung without notable pathological lesion on day 14 after a single intratracheal instillation. Pulmonary total cell number increased significantly with the highest dose, but the levels of all measured inflammatory cytokines and chemokines, except IL-1, were lower in BAL fluid from SGP-treated mice compared to control. More interestingly, the expression of antigen presentation-related proteins was enhanced in the lungs of SGP-exposed mice concomitant with an increase in the number of mature dendritic cells, whereas the expression of ICAM-1, an important adhesion molecule for helper T cell recruitment, was suppressed. Taken together, we suggest that SGPs may induce adverse health effects by down-regulating function of immune cells in the lungs. Furthermore, ICAM-1 may play a key role in immune response to remove pulmonary SGPs.

Original languageEnglish
JournalEnvironmental Toxicology
DOIs
Publication statusAccepted/In press - 2017

Fingerprint

Glass
glass
Lung
Silicon Dioxide
silica
Intercellular Adhesion Molecule-1
Alveolar Macrophages
Health
immune response
Crystalline materials
Respiratory system
Alveolar Epithelial Cells
Dimercaprol
Molecules
T-cells
particle
Antigen Presentation
Biological Factors
Adaptive Immunity
carcinogen

Keywords

  • Adhesion molecules
  • Amorphous silica
  • Antigen presentation
  • Glass particles
  • Inflammation

ASJC Scopus subject areas

  • Toxicology
  • Management, Monitoring, Policy and Law
  • Health, Toxicology and Mutagenesis

Cite this

Pulmonary glass particles may persist in the lung suppressing function of immune cells. / Park, Eun Jung; Lee, Gwang Hee; Kim, Jae Chan; Jin Lee, Sang; Lee, Kyuhong; Lee, Byoung Seok; Chang, Jaerak; Kim, Dong-Wan.

In: Environmental Toxicology, 2017.

Research output: Contribution to journalArticle

Park, Eun Jung ; Lee, Gwang Hee ; Kim, Jae Chan ; Jin Lee, Sang ; Lee, Kyuhong ; Lee, Byoung Seok ; Chang, Jaerak ; Kim, Dong-Wan. / Pulmonary glass particles may persist in the lung suppressing function of immune cells. In: Environmental Toxicology. 2017.
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