Particulate air pollution contains iron that may be involved in the patholo
gical effects after inhalation. This article reviews work demonstrating tha
t ambient particulate samples (Standard Reference Material [SRM] 1648 and S
RM 1649, from the National Institute of Science Science and Technology) con
tain iron that can be mobilized from the particle in vitro and inside human
lung epithelial (A549) cells. The mobilized iron can then catalyze the for
mation of reactive oxygen species (ROS). Work is also reviewed on the gener
ation and sire fractionation of coal fly ash (CFA) from three commercially
important coal types, as well as size fractionation of three types of nonco
mbustion particles. The availability of iron from these particles to A549 c
ells was measured by citrate mobilization in vitro and induction of the iro
n storage protein Ferritin in particle-treated cells. The amount of bioavai
lable iron decreased with increasing particle size. The ability of particle
s to induce synthesis of the proinflammatory cytokine interleukin-8 (IL-8)
was also determined. As with the bioavailability of iron, there was an inve
rse correlation with size. Further work showed that iron in CFA is responsi
ble for IL-8 induction. Mossbauer spectroscopy of a CFA sample before and a
fter desferrioxamine B treatment to remove bioavailable iron showed that th
e bioavailable iron was associated with the glassy aluminosilicate fraction
of the particle. In conclusion, this work shows that bioavailable iron is
responsible for ROS production by SRMs and IL-8 induction by CFA in A549 ce
lls. The source of this bioavailable iron in CFA is glassy aluminosilicates
, which are found at higher levels in smaller sizes of CFA.