Eosinophil peroxidase stimulates the release of granulocyte-macrophage colony- stimulating factor from bronchial epithelial cells  Shinji Motojima, MDa,

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Presentation transcript:

Eosinophil peroxidase stimulates the release of granulocyte-macrophage colony- stimulating factor from bronchial epithelial cells  Shinji Motojima, MDa, Tetsuya Adachi, MDa, Ken-ichi Manaka, PhDb, Masafumi Arima, MDa, Takeshi Fukuda, MDa, Sohei Makino, MDa  Journal of Allergy and Clinical Immunology  Volume 98, Issue 6, Pages S216-S223 (December 1996) DOI: 10.1016/S0091-6749(96)70069-6 Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 1 Effect of EPO on release of GM-CSF from BEAS-2B cells. BEAS-2B cells were first washed with phosphate-buffered saline. EPO was then applied to BEAS-2B cells and incubated for 15 minutes at 37° C. Cells were washed twice with HD-F12 medium and were again incubated with 1 ml of HD-F12 at 37° C. Supernatants were harvested at 3, 6, or 24 hours, and concentration of GM-CSF was measured. Journal of Allergy and Clinical Immunology 1996 98, S216-S223DOI: (10.1016/S0091-6749(96)70069-6) Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 2 Effect of various substances on release of GM-CSF from BEAS-2B cells in 24-hour culture supernatants. BEAS-2B cells were exposed to EPO, poly-L-arginine, poly-L-lysine, and poly-L-glutamic acid for 15 minutes and washed before incubation with 1 ml of HD-F12. Human recombinant IL-1β and catalase were cocultured with cells for entire 24-hour incubation period. Cells were exposed to CHX for 30 minutes before exposure to EPO and then were cultured in its presence for 24 hours. Heparin was mixed with EPO before addition to wells with BEAS-2B cells. Journal of Allergy and Clinical Immunology 1996 98, S216-S223DOI: (10.1016/S0091-6749(96)70069-6) Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 3 Effect of EPO + H2O2 + halide system on release of GM-CSF from BEAS-2B cells in 24-hour culture supernatants. BEAS-2B cells were first washed with phosphate-buffered saline. EPO was then applied to BEAS-2B cells and incubated for 15 minutes at 37° C. Cells were washed twice with HD-F12 medium and were again incubated with 1 ml of HD-F12 at 37° C in presence of 10-5 mol/L H2O2 and 10-4 mol/L NaBr. To compare with EPO system, individual components included in EPO system were added separately. Journal of Allergy and Clinical Immunology 1996 98, S216-S223DOI: (10.1016/S0091-6749(96)70069-6) Copyright © 1996 Mosby, Inc. Terms and Conditions

FIG. 4 Expression of mRNA for GM-CSF and β-actin detected by Northern blotting. RNA extracted from BEAS-2B cells pretreated with 5.9 × 10-7 mol/L or those incubated with medium alone (control) were subjected to Northern blotting. Journal of Allergy and Clinical Immunology 1996 98, S216-S223DOI: (10.1016/S0091-6749(96)70069-6) Copyright © 1996 Mosby, Inc. Terms and Conditions