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刚地弓形虫:BAG-5的体内表达及包囊形成独立于肿瘤坏死因子p55受体和诱导型一氧化氮合酶功能。

Toxoplasma gondii: in vivo expression of BAG-5 and cyst formation is independent of TNF p55 receptor and inducible nitric oxide synthase functions.

作者信息

Silva Neide M, Tafuri Wagner L, Alvarez-Leite Jacqueline I, Mineo José R, Gazzinelli Ricardo T

机构信息

Department of Biochemistry and Immunology, Federal University of Minas Gerais, Avenue Antônio Carlos 6627, Belo Horizonte, MG 31270-010, Brazil.

出版信息

Microbes Infect. 2002 Mar;4(3):261-70. doi: 10.1016/s1286-4579(02)01537-x.

Abstract

Wild type, TNFRp55(-/-), iNOS(-/-) and IFN-gamma(-/-) mice were infected with Toxoplasma gondii strain ME-49, and the central nervous system (CNS), lungs, liver, spleen, heart and kidneys were examined for the presence of parasites expressing tachyzoite-specific (SAG-1) and bradyzoite-specific (BAG-5) antigens. During the acute phase of infection, the peripheral organs, but not the CNS, of the IFN-gamma(-/-) mice are heavily parasitized by tachyzoites and there are no signs of parasites expressing BAG-5. In contrast, the tissues from TNFRp55(-/-) and inducible nitric oxide synthase (iNOS)(-/-) mice, mainly the CNS, presented high numbers of parasites expressing SAG-1 and/or BAG-5. Tachyzoite transformation into bradyzoite and cyst development was shown to be normal in the tissues from TNFRp55(-/-) and iNOS(-/-) mice, as indicated by the high numbers of BAG-5/PAS positive cysts. Consistently, reactivation of infection in IFN-gamma(-/-) mice was rapid and characterized by a dramatic increase in SAG-1, contrasting with slow course in the TNFRp55(-/-) or iNOS(-/-) mice associated with a relatively small increase in SAG-1- and/or BAG-5-positive parasites. In conclusion, our results suggest that the control of multiplication of tachyzoites is largely dependent on endogenous IFN-gamma with partial involvement of TNFRp55 and iNOS. In contrast, induction of BAG-5 expression and cyst formation during toxoplasmosis seems to be dependent on IFN-gamma, but independent of TNFRp55 and iNOS functions.

摘要

野生型、肿瘤坏死因子受体p55基因敲除(TNFRp55(-/-))、诱导型一氧化氮合酶基因敲除(iNOS(-/-))和γ干扰素基因敲除(IFN-γ(-/-))小鼠感染刚地弓形虫ME-49株,检查其中枢神经系统(CNS)、肺、肝、脾、心脏和肾脏中表达速殖子特异性抗原(SAG-1)和缓殖子特异性抗原(BAG-5)的寄生虫。在感染急性期,IFN-γ(-/-)小鼠的外周器官而非中枢神经系统被大量速殖子寄生,且无表达BAG-5的寄生虫迹象。相反,TNFRp55(-/-)和诱导型一氧化氮合酶(iNOS)基因敲除小鼠的组织,主要是中枢神经系统,出现大量表达SAG-1和/或BAG-5的寄生虫。如大量BAG-5/PAS阳性包囊所示,TNFRp55(-/-)和iNOS(-/-)小鼠组织中速殖子向缓殖子的转化及包囊形成正常。同样,IFN-γ(-/-)小鼠感染的再激活迅速,其特征是SAG-1显著增加,这与TNFRp55(-/-)或iNOS(-/-)小鼠病程缓慢形成对比,后者SAG-1和/或BAG-5阳性寄生虫增加相对较少。总之,我们的结果表明,速殖子增殖的控制很大程度上依赖内源性γ干扰素,TNFRp55和iNOS部分参与其中。相反,弓形虫病期间BAG-5表达及包囊形成的诱导似乎依赖γ干扰素,但与TNFRp55和iNOS功能无关。

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