Cloning of rat eotaxin: ozone inhalation increases mRNA and protein expression in lungs of brown Norway rats

被引:28
作者
Ishii, Y [1 ]
Shirato, M
Nomura, A
Sakamoto, T
Uchida, Y
Ohtsuka, M
Sagai, M
Hasegawa, S
机构
[1] Univ Tsukuba, Inst Clin Med Sci, Dept Resp Med, Tsukuba, Ibaraki 305, Japan
[2] Natl Inst Environm Studies, Tsukuba, Ibaraki 305, Japan
关键词
messenger ribonucleic acid; chemokine; cytokine; inflammation; eosinophils;
D O I
10.1152/ajplung.1998.274.1.L171
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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 whether 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 mature eotaxin protein with 97.3% identity to mouse eotaxin. The recombinant protein encoded by this gene displayed specific chemotactic activity for eosinophils when analyzed with a microchemotactic chamber. The expression of eotaxin mRNA increased similar to 1.6-fold immediately after 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 greater, respectively, than control eosinophils. Immunocytochemistry revealed that alveolar macrophages and bronchial epithelial cells were positive 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.
引用
收藏
页码:L171 / L176
页数:6
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