Abstract

BackgroundOccupational exposure to crystalline silica is a well-established occupational hazard. Once in the lung, crystalline silica particles can result in the activation of alveolar macrophages (AM), potentially leading to silicosis, a fibrotic lung disease. Because the activation of alveolar macrophages is the beginning step in a complicated inflammatory cascade, it is necessary to define the particle characteristics resulting in this activation. The aim of this research was to determine the effect of the size of crystalline silica particles on the activation of macrophages.MethodsRAW 264.7 macrophages were exposed to four different sizes of crystalline silica and their activation was measured using electron microscopy, reactive oxygen species (ROS) generation by mitochondria, and cytokine expression.ResultsThese data identified differences in particle uptake and formation of subcellular organelles based on particle size. In addition, these data show that the smallest particles, with a geometric mean of 0.3 μm, significantly increase the generation of mitochondrial ROS and the expression of cytokines when compared to larger crystalline silica particles, with a geometric mean of 4.1 μm.ConclusionIn summary, this study presents novel data showing that crystalline silica particles with a geometric mean of 0.3 μm enhance the activation of AM when compared to larger silica particles usually represented in in vitro and in vivo research.

Highlights

  • Occupational exposure to crystalline silica is a well-established occupational hazard

  • transmission electron microscopy (TEM) Images of RAW cells after exposure with two sizes of crystalline silica In order to visualize the difference in the handling of UF particles and C particles by alveolar macrophages (AM), RAW 264.7 AM were exposed to UF and C particles for one, two, and four hours

  • This study provided novel data showing that UF silica particles enhance the activation of AM when compared to larger silica particles usually represented in in vitro and in vivo research

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Summary

Introduction

Occupational exposure to crystalline silica is a well-established occupational hazard. Crystalline silica particles can result in the activation of alveolar macrophages (AM), potentially leading to silicosis, a fibrotic lung disease. Occupational exposure to crystalline silica (CS) affects at least 1.7 million US workers [1] and is associated with the development of silicosis, a fibrotic lung disease which is one of the most important occupational diseases worldwide [2,3,4]. The National Institute for Occupational Safety and Health (NIOSH) reported that 300 silicosis-related deaths occurred each year in the United States between 1991 and 1995 [5]. During those same years China recorded 24,000 silicosis-related deaths per year [6]. Silica exposure will occur in any occupation that includes grinding or mechanically breaking material containing silica (mining, construction) or handling fine particles containing silica, such as silica sand (fracking) [4, 8,9,10,11,12]

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