Differential Roles of Water-Insoluble
and Water-Soluble Fractions of Diesel Exhaust Particles in the Development
of Adverse Health Effects Due to Chronic Instillation of Diesel Exhaust
Particles
Ambient fine particulate
matter (PM2.5) has a marked temporospatial variation in
chemical composition,
but how the composition of PM2.5 influences its toxicity
remains elusive. To explore the roles of individual PM2.5 components in the pathogenesis following PM2.5 exposure,
we prepared water-soluble (WS-DEP) and water-insoluble (WIS-DEP) fractions
of diesel exhaust particles (DEP) and performed 15-week intratracheal
instillation on C57Bl/6J mice using these fractions. Their effects
on pulmonary and systemic inflammation, hepatic steatosis and insulin
resistance, systemic glucose homeostasis, and gut microbiota were
then assessed. Compared to control, instillation of DEP or WIS-DEP,
but not WS-DEP, significantly increased pulmonary inflammatory scores
and expression of inflammatory markers, bronchoalveolar lavage fluid
cell number, and circulating pro-inflammatory cytokines. Consistently,
DEP- or WIS-DEP-instilled but not WS-DEP-instilled mice versus control
had significant hepatic steatosis and insulin resistance and systemic
glucose intolerance. In contrast, instillation of WS-DEP versus instillation
of WIS-DEP had effects on the gut microbiota more comparable to that
of instillations of DEP. The pulmonary and systemic inflammation,
hepatic steatosis and insulin resistance, and systemic glucose intolerance
following chronic DEP instillation are all attributable to the WIS-DEP,
suggesting that PM2.5 may have a solubility-dependent basal
toxicity.