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KMID : 0425120090470030205
Parasites, Hosts and Diseases
2009 Volume.47 No. 3 p.205 ~ p.212
Proinflammatory Cytokine and Nitric Oxide Production by Human Macrophages Stimulated with Trichomonas vaginalis
Han Ik-Hwan

Yang Sung-Woo Michael
Kim Yong-Seok
Hwang Se-Jin
Park Soon-Jung
Goo Sung-Young
Ahn Myoung-Hee
Ryu Jae-Sook
Abstract
Trichomonas vaginalis commonly causes vaginitis and perhaps cervicitis in women and urethritis in men and women. Macrophages are important immune cells in response to T. vaginalis infection. In this study, we investigated whether human macrophages could be involved in inflammation induced by T. vaginalis. Human monocyte-derived macrophages (HMDM) were co-cultured with T. vaginalis. Live, opsonized-live trichomonads, and T. vaginalis lysates increased proinflammatory cytokines, such as TNF-¥á, IL-1¥â, and IL-6 by HMDM. The involvement of nuclear factor (NF)-¥êB signaling pathway in cytokine production induced by T. vaginalis was confirmed by phosphorylation and nuclear translocation of p65 NF-¥êB. In addition, stimulation with live T. vaginalis induced marked augmentation of nitric oxide (NO) production and expression of inducible NO synthase (iNOS) levels in HMDM. However, trichomonad-induced NF-¥êB activation and TNF-¥á production in macrophages were significantly inhibited by inhibition of iNOS levels with L-NMMA (NO synthase inhibitor). Moreover, pretreatment with NF-¥êB inhibitors (PDTC or Bay11-7082) caused human macrophages to produce less TNF-¥á. These results suggest that T. vaginalis stimulates human macrophages to produce proinflammatory cytokines, such as IL-1, IL-6, and TNF-¥á, and NO. In particular, we showed that T. vaginalis induced TNF-¥á production in macrophages through NO-dependent activation of NF-¥êB, which might be closely involved in inflammation caused by T. vaginalis.
KEYWORD
Trichomonas vaginalis, human monocyte-derived macrophage, proinflammatory cytokine, nitric oxide, iNOS, NF-¥êB
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