Vitamin D treatment modulates organic dust-induced cellular and airway inflammatory consequences

J Biochem Mol Toxicol. 2013 Jan;27(1):77-86. doi: 10.1002/jbt.21467. Epub 2012 Dec 20.

Abstract

Exposure to organic dusts elicits airway inflammatory diseases. Vitamin D recently has been associated with various airway inflammatory diseases, but its role in agricultural organic dust exposures is unknown. This study investigated whether vitamin D reduces organic dust-induced inflammatory outcomes in cell culture and animal models. Organic dust extracts obtained from swine confinement facilities induced neutrophil chemokine production (human IL-8, murine CXCL1/CXCL2). Neutrophil chemokine induction was reduced in human blood monocytes, human bronchial epithelial cells, and murine lung slices pretreated with 1,25-(OH)(2) D(3) . Intranasal inhalation of organic dust extract induced neutrophil influx, and CXCL1/CXCL2 release was also decreased in mice fed a relatively high vitamin D diet as compared to mice fed a low vitamin D diet. These findings were associated with reduced tracheal epithelial cell PKCα and PKCε activity and whole lung TLR2 and TLR4 gene expression. Collectively, vitamin D plays a role in modulating organic dust-induced airway inflammatory outcomes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Administration, Intranasal
  • Animals
  • Cell Line
  • Chemokine CXCL1 / metabolism
  • Chemokine CXCL2 / metabolism
  • Chemokines / metabolism*
  • Disease Models, Animal
  • Dust*
  • Humans
  • In Vitro Techniques
  • Inflammation / drug therapy*
  • Inflammation / etiology*
  • Inflammation / immunology
  • Interleukin-8 / metabolism
  • Lung / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Monocytes / drug effects
  • Organic Agriculture
  • Protein Kinase C / metabolism
  • Swine
  • Toll-Like Receptor 2 / genetics
  • Toll-Like Receptor 4 / genetics
  • Vitamin D / pharmacology*

Substances

  • Chemokine CXCL1
  • Chemokine CXCL2
  • Chemokines
  • Cxcl1 protein, mouse
  • Cxcl2 protein, mouse
  • Dust
  • Interleukin-8
  • TLR2 protein, human
  • TLR4 protein, human
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • Vitamin D
  • Protein Kinase C