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牛巴贝斯虫对巨噬细胞中一氧化氮产生的刺激作用。

Stimulation of nitric oxide production in macrophages by Babesia bovis.

作者信息

Stich R W, Shoda L K, Dreewes M, Adler B, Jungi T W, Brown W C

机构信息

Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington 99164-7040, USA.

出版信息

Infect Immun. 1998 Sep;66(9):4130-6. doi: 10.1128/IAI.66.9.4130-4136.1998.

Abstract

Gamma interferon (IFN-gamma)-activated macrophages are believed to play a key role in resistance to Babesia bovis through parasite suppression by macrophage secretory products. However, relatively little is known about interactions between this intraerythrocytic parasite and the macrophages of its bovine host. In this study, we examined the in vitro effect of intact and fractionated B. bovis merozoites on bovine macrophage nitric oxide (NO) production. In the presence of IFN-gamma, B. bovis merozoites stimulated NO production, as indicated by the presence of increased L-arginine-dependent nitrite (NO2-) levels in culture supernatants of macrophages isolated from several cattle. The merozoite crude membrane (CM) fraction stimulated greater production of NO, in a dose-dependent manner, than did the merozoite homogenate or the soluble, cytosolic high-speed supernatant fraction. Stimulation of NO production by CM was enhanced by as little as 1 U of IFN-gamma per ml of culture medium. Upregulation of inducible NO synthase mRNA in bovine macrophages by either B. bovis-parasitized erythrocytes and IFN-gamma or CM was also observed. B. bovis-specific T-helper lymphocyte culture supernatants, all of which contained IFN-gamma, were also found to induce L-arginine-dependent NO2- production. Supernatants that induced the highest levels of NO also contained biologically active TNF. These results show that B. bovis merozoites and antigen-stimulated B. bovis-immune T cells can induce the production of NO, a molecule implicated in both protection and pathologic changes associated with hemoprotozoan parasite infections.

摘要

γ干扰素(IFN-γ)激活的巨噬细胞被认为通过巨噬细胞分泌产物抑制寄生虫,在抵抗牛巴贝斯虫中发挥关键作用。然而,关于这种红细胞内寄生虫与其牛宿主巨噬细胞之间的相互作用,人们了解得相对较少。在本研究中,我们检测了完整的和分级分离的牛巴贝斯虫裂殖子对牛巨噬细胞一氧化氮(NO)产生的体外影响。在IFN-γ存在的情况下,牛巴贝斯虫裂殖子刺激了NO的产生,从几头牛分离的巨噬细胞培养上清液中L-精氨酸依赖性亚硝酸盐(NO2-)水平升高表明了这一点。裂殖子粗膜(CM)组分比裂殖子匀浆或可溶性胞质高速上清液组分以剂量依赖性方式刺激产生更多的NO。每毫升培养基中低至1 U的IFN-γ就能增强CM对NO产生的刺激作用。还观察到,被牛巴贝斯虫寄生的红细胞和IFN-γ或CM均可上调牛巨噬细胞中诱导型NO合酶mRNA的表达。还发现,所有都含有IFN-γ的牛巴贝斯虫特异性辅助性T淋巴细胞培养上清液也能诱导L-精氨酸依赖性NO2-的产生。诱导最高水平NO的上清液中也含有生物活性肿瘤坏死因子(TNF)。这些结果表明,牛巴贝斯虫裂殖子和抗原刺激的牛巴贝斯虫免疫T细胞可诱导NO的产生,NO是一种与血原虫寄生虫感染相关的保护和病理变化均有关的分子。

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