Y. Ishii et al., CLONING OF RAT EOTAXIN - OZONE INHALATION INCREASES MESSENGER-RNA ANDPROTEIN EXPRESSION IN LUNGS OF BROWN-NORWAY RATS, American journal of physiology. Lung cellular and molecular physiology, 18(1), 1998, pp. 171-176
The C-C chemokine eotaxin is thought to be important in the selective
recruitment of eosinophils to the site of inflammation in guinea pigs,
mice, and humans. We isolated the rat eotaxin gene to determine wheth
er a similar molecule might play a role in the pulmonary infiltration
of eosinophils during acute inflammation in the rat. The cDNA for rat
eotaxin encoded a 97-amino acid protein containing a 74-amino acid mat
ure eotaxin protein with 97.3% identity to mouse eotaxin. The recombin
ant protein encoded by this gene displayed specific chemotactic activi
ty for eosinophils when analyzed with a microchemotactic chamber. The
expression of eotaxin mRNA increased similar to 1.6-fold immediately a
fter exposure to ozone and was 4-fold higher after 20 h. The number of
lavageable eosinophils at the same time points were 3- and 15-fold gr
eater, respectively, than control eosinophils. Immunocytochemistry rev
ealed that alveolar macrophages and bronchial epithelial cells were po
sitive for eotaxin. These results suggest that eotaxin may be involved
in the recruitment of eosinophils into the air spaces during certain
inflammatory conditions in rats.