Suppressive Effect of Arazyme on Neutrophil Apoptosis in Normal and Allergic Subjects
Author(s) -
In Sik Kim,
Ji-Sook Lee
Publication year - 2014
Publication title -
journal of experimental and biomedical sciences/biomedical science letters
Language(s) - English
Resource type - Journals
eISSN - 2288-7415
pISSN - 1738-3226
DOI - 10.15616/bsl.2014.20.4.244
Subject(s) - apoptosis , protein kinase b , pi3k/akt/mtor pathway , ly294002 , mapk/erk pathway , medicine , immunology , caspase , cancer research , signal transduction , chemistry , biology , microbiology and biotechnology , programmed cell death , biochemistry
Arazyme is a metalloprotease secreted by Aranicola proteolyticus that was previously shown to suppress cytokine expression of keratinocytes and endothelial cells and inhibit histopathological features in an atopic dermatitis-like animal model. However, the regulatory effects of arazyme in other allergic diseases have yet to be elucidated. In this study, we investigated whether arazyme is effective against neutrophil apoptosis in allergic diseases such as allergic rhinitis and asthma. Arazyme inhibited neutrophil apoptosis of normal subjects in a dose-dependent manner. However, the antiapoptotic effect of arazyme was reversed by LY294002, an inhibitor of PI3K, AKTi, an inhibitor of Akt, PD98059, an inhibitor of MEK, and BAY-11-7085, an inhibitor of NF-κB. Arazyme induced activation of NF-κB via PI3K/Akt/ERK pathway. The anti-apoptotic effect of arazyme is associated with inhibition of cleavage of caspase 3 and caspase 9. Arazyme inhibited constitutive apoptosis of neutrophil in a dose-dependent manner in allergic subjects, and its mechanism was shown to be associated with PI3K/Akt/ERK/NF-κB. The results presented here improve our understanding of neutrophil apoptosis regulation and will facilitate development of drugs for treatment of allergic diseases.
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