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弓形虫体内感染期间吲哚胺2,3-双加氧酶的表达、色氨酸降解及犬尿氨酸的形成:内源性γ干扰素的诱导作用及干扰素调节因子1的需求

Expression of indoleamine 2,3-dioxygenase, tryptophan degradation, and kynurenine formation during in vivo infection with Toxoplasma gondii: induction by endogenous gamma interferon and requirement of interferon regulatory factor 1.

作者信息

Silva Neide M, Rodrigues Cibele V, Santoro Marcelo M, Reis Luiz F L, Alvarez-Leite Jacqueline I, Gazzinelli Ricardo T

机构信息

Department of Biochemistry and Immunology, UFMG, 31270-910 Belo Horizonte. Centro de Pesquisas René Rachou, FIOCRUZ, 30190-002 Belo Horizonte, Brazil.

出版信息

Infect Immun. 2002 Feb;70(2):859-68. doi: 10.1128/IAI.70.2.859-868.2002.

Abstract

The induction of indoleamine 2,3-dioxygenase (INDO) expression and the tryptophan (Trp)-kynurenine (Kyn) metabolic pathway during in vivo infection with Toxoplasma gondii was investigated. Decreased levels of Trp and increased formation of Kyn were observed in the lungs, brain, and serum from mice infected with T. gondii. Maximal INDO mRNA expression and enzyme activity were detected in the lungs at 10 to 20 days postinfection. Further, the induction of INDO mRNA expression, Trp degradation and Kyn formation were completely absent in tissues from mice deficient in IFN-gamma (IFN-gamma(-/-)) or IFN regulatory factor -1 (IRF-1(-/-)). These findings indicate the important role of endogenous IFN-gamma and IRF-1 in the in vivo induction of the Trp-Kyn metabolic pathway during acute infection with T. gondii. In contrast, expression of INDO mRNA and its activity was preserved in the tissues of TNF-receptor p55- or inducible nitric oxide synthase-deficient mice infected with T. gondii. Together with the results showing the extreme susceptibility of the IFN-gamma(-/-) and the IRF-1(-/-) mice to infection with T. gondii, our results indicate a possible involvement of INDO and Trp degradation in host resistance to early infection with this parasite.

摘要

研究了刚地弓形虫体内感染过程中吲哚胺2,3-双加氧酶(INDO)表达及色氨酸(Trp)-犬尿氨酸(Kyn)代谢途径的诱导情况。在感染刚地弓形虫的小鼠的肺、脑和血清中观察到Trp水平降低以及Kyn生成增加。在感染后10至20天,肺中检测到最大的INDO mRNA表达和酶活性。此外,在缺乏干扰素-γ(IFN-γ(-/-))或干扰素调节因子-1(IRF-1(-/-))的小鼠组织中,完全不存在INDO mRNA表达的诱导、Trp降解和Kyn生成。这些发现表明内源性IFN-γ和IRF-1在刚地弓形虫急性感染期间Trp-Kyn代谢途径的体内诱导中起重要作用。相比之下,在感染刚地弓形虫的肿瘤坏死因子受体p55缺陷或诱导型一氧化氮合酶缺陷小鼠的组织中,INDO mRNA的表达及其活性得以保留。连同显示IFN-γ(-/-)和IRF-1(-/-)小鼠对刚地弓形虫感染极度易感的结果,我们的结果表明INDO和Trp降解可能参与宿主对该寄生虫早期感染的抵抗。

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