Ramarathinam L, Niesel D W, Klimpel G R
Department of Microbiology, University of Texas Medical Branch, Galveston 77555-1019.
J Immunol. 1993 May 1;150(9):3965-72.
The Ity-Lsh-Bcg genetic locus in the mouse has been documented to confer innate resistance to at least three intracellular pathogens: Salmonella typhimurium, Leishmania donovani, and Mycobacterium. Expression of the resistance gene(s) results in a slower net growth of these pathogens in the reticuloendothelial system early postinfection. Although it is clear that the resident macrophages in resistant mice are functionally superior with regard to antimicrobial activity, the exact mechanism(s) underlying the control exerted by this gene is not understood. Using S. typhimurium infection as a model, we have examined the influence of this resistance gene(s) on the production of IFN-gamma, a cytokine known to play an important role in host-defense against several intracellular pathogens. We compared IFN-gamma production by splenocytes from resistant (Ity(r)) and sensitive (Ity(s)) inbred mouse strains after stimulation in vitro with S. typhimurium. Spleen cells from Ity(r) mouse strains produced significantly higher levels of IFN-gamma when compared to spleen cells obtained from Ity(s) mouse strains. Enhanced IFN-gamma production was not a generalized response to bacteria. Listeria monocytogenes induced comparable levels of IFN-gamma production from both Ity(r) (CBA/J) and Ity(s) (C57BL/6) mice. Splenocytes from Ity congenic mouse strains displayed similar differences in the level of IFN-gamma produced after S. typhimurium stimulation, with spleen cells from the Ity(r) strain producing significantly higher levels of IFN-gamma when compared to spleen cells from the Ity(s) strain. A requirement for adherent cells and/or adherent cell-derived factors has been documented for IFN-gamma production by S. typhimurium-stimulated splenocytes. Interestingly, supernatant from adherent cells obtained from Ity(r) mouse strains was found to induce the production of significantly higher levels of IFN-gamma when compared to adherent cell supernatant from Ity(s) strains. Nylon wool nonadherent cells from Ity(s) mouse strains produced high levels of IFN-gamma when exposed to supernatants obtained from adherent cells of Ity(r) mouse strains. In contrast, nylon wool nonadherent cells from Ity(r) mouse strains produced reduced levels of IFN-gamma when exposed to supernatant obtained from adherent cells of Ity(s) mouse strains. Thus, modulation of IFN-gamma production appears to be a function of the Ity(r) gene(s). This study documents for the first time that the Ity locus may play a role in controlling resistance to Salmonella infection by regulating IFN-gamma production by NK cells.
小鼠中的Ity-Lsh-Bcg基因座已被证明可赋予对至少三种细胞内病原体的先天抗性:鼠伤寒沙门氏菌、杜氏利什曼原虫和分枝杆菌。抗性基因的表达导致这些病原体在感染后早期在网状内皮系统中的净生长较慢。虽然很明显抗性小鼠中的驻留巨噬细胞在抗菌活性方面功能更优越,但该基因所施加控制的具体机制尚不清楚。以鼠伤寒沙门氏菌感染为模型,我们研究了该抗性基因对IFN-γ产生的影响,IFN-γ是一种已知在宿主抵御几种细胞内病原体中起重要作用的细胞因子。我们比较了用鼠伤寒沙门氏菌体外刺激后,抗性(Ity(r))和敏感(Ity(s))近交小鼠品系脾细胞产生的IFN-γ。与从Ity(s)小鼠品系获得的脾细胞相比,Ity(r)小鼠品系的脾细胞产生的IFN-γ水平显著更高。IFN-γ产生的增强不是对细菌的普遍反应。单核细胞增生李斯特菌诱导Ity(r)(CBA/J)和Ity(s)(C57BL/6)小鼠产生相当水平的IFN-γ。Ity同源小鼠品系的脾细胞在鼠伤寒沙门氏菌刺激后产生的IFN-γ水平上表现出类似差异,与Ity(s)品系的脾细胞相比,Ity(r)品系的脾细胞产生的IFN-γ水平显著更高。鼠伤寒沙门氏菌刺激的脾细胞产生IFN-γ需要贴壁细胞和/或贴壁细胞衍生因子。有趣的是,与Ity(s)品系的贴壁细胞上清液相比,从Ity(r)小鼠品系获得的贴壁细胞上清液被发现可诱导产生显著更高水平的IFN-γ。当暴露于从Ity(r)小鼠品系的贴壁细胞获得的上清液时,Ity(s)小鼠品系的尼龙毛非贴壁细胞产生高水平的IFN-γ。相反,当暴露于从Ity(s)小鼠品系的贴壁细胞获得的上清液时,Ity(r)小鼠品系的尼龙毛非贴壁细胞产生的IFN-γ水平降低。因此,IFN-γ产生的调节似乎是Ity(r)基因的功能。这项研究首次证明Ity基因座可能通过调节NK细胞产生IFN-γ在控制对沙门氏菌感染的抗性中发挥作用。