Mechanisms of ozone-induced inhibitory effect of bronchoalveolar lavage fluid on alveolar macrophage-mediated immunosuppressive activity in rats

被引:7
作者
Koike, E
Kobayashi, T [1 ]
Murakami, M
McWilliam, AS
Holt, PG
机构
[1] Natl Inst Environm Studies, Environm Hlth Sci Div, Tsukuba, Ibaraki 3050053, Japan
[2] Univ Tsukuba, Dept Med Sci, Tsukuba, Ibaraki 305, Japan
[3] Univ Tsukuba, Inst Community Med, Tsukuba, Ibaraki 305, Japan
[4] TVW Telethon Inst Child Hlth Res, Perth, WA, Australia
关键词
nitric oxide; lymph node cell; interferon-8;
D O I
10.1002/jlb.66.1.75
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Resident alveolar macrophages (AM) Play an important immunomodulatory role via suppression of lymphocyte proliferation, and nitric oxide (NO) plays a crucial role in this immunosuppression of AM. Our previous report suggested that during ozone (O-3)-induced lung inflammation, bronchoalveolar lava,ae fluid (BALF) inhibited AM-mediated immunosuppression and concanavalin A (Con A)-induced proliferation of lymph node cells (LNC) [E, Koike et al, (1998) Toxicol, Sci, 41, 217-223], In these studies, we investigated the mechanisms of the inhibition of BALF from O-3-exposed rats (O-3-BALF), We investigated whether BALF nlight affect (1) the interferon-gamma (IFN-gamma) production by Con A-stimulated LNC and IFN-gamma-induced NO production by AM, and (2) the interleukin (IL)-2 production by Con A-stimulated LNC and IL-2-induced LNC proliferation. These results demonstrated that O-3-BALF inhibited IFN-gamma production by Con A-stinlulated LNC, IFN-gamma-induced NO production by AM, and IL-2-induced LNC proliferation. In addition, the major inhibitory factor against AM-mediated immunosuppression in O-3-BALF may be a protein of greater than 10 kDa.
引用
收藏
页码:75 / 82
页数:8
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