Toxocara canis antigens stimulate the production of nitric oxide and prostaglandin E2 by rat alveolar macrophages

被引:22
作者
Espinoza, E
Muro, A
Martín, MMS
Casanueva, P
Pérez-Arellano, JL
机构
[1] Univ Salamanca, Fac Farm, Parasitol Lab, E-37007 Salamanca, Spain
[2] Univ Las Palmas de Gran Canaria, Dept Ciencias Med & Quirurg, Unidad Enfermedades Infecciosas & Med Trop, Las Palmas Gran Canaria, Spain
关键词
Toxocara canis; nitric oxide; prostaglandin E-2; alveolar macrophages;
D O I
10.1046/j.1365-3024.2002.00468.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The effect of four Toxocara canis antigens on nitric oxide (NO) and prostaglandin E-2 (PGE(2) ) synthesis was studied in vitro using rat alveolar macrophages. Somatic and excretory/secretory T. canis antigens prepared from adult worms and LII larvae were incubated with rat alveolar macrophages obtained by bronchoalveolar lavage at concentrations of 0.1-50 mug/ml. Both excretory/secretory adult antigen (ESA) and somatic LII antigen (SLII) stimulate the release of nitrites by alveolar macrophages. This effect was specific (inhibited by l-NAME and l-canavanine) and dose-dependent; 30 mug and 10 mug being the most effective concentrations of ESA and SLII, respectively. Western blot and reverse transcriptase-polymerase chain reaction analyses revealed that ESA antigen stimulates the production of NO at transcriptional level. T. canis ESA also stimulated macrophages to produce PGE(2) at transcriptional level. The addition of l-canavanine decreased the release of PGE(2) significantly, which suggests that NO mediates the production of this prostaglandin. These results indicate that T. canis can stimulate the release of vasodilatory mediators by macrophages of the host.
引用
收藏
页码:311 / 319
页数:9
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