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细胞内利什曼原虫属对小鼠腹腔巨噬细胞氧化代谢的损害

Impairment of the oxidative metabolism of mouse peritoneal macrophages by intracellular Leishmania spp.

作者信息

Buchmüller-Rouiller Y, Mauël J

出版信息

Infect Immun. 1987 Mar;55(3):587-93. doi: 10.1128/iai.55.3.587-593.1987.

Abstract

When stimulated in vitro with macrophage-activating factor or lipopolysaccharide, mouse peritoneal macrophages acquire the capacity to develop a strong respiratory burst when they are triggered by membrane-active agents. The presence of intracellular parasites of the genus Leishmania (L. enriettii, L. major) significantly inhibited such activity, as measured by chemiluminescence, reduction of cytochrome c and Nitro Blue Tetrazolium, and hexose monophosphate shunt levels. On the contrary, inert intracellular particles such as latex beads strongly increased the macrophage respiratory burst, suggesting that the Leishmania-linked inhibition resulted from a specific parasite effect. Impairment of macrophage oxidative metabolism by intracellular Leishmania spp. was a function of the number of infecting microorganisms and was more pronounced in macrophages infected with living than with dead parasites. Moreover, the metabolic inhibition was less apparent in L. enriettii-infected macrophages that were exposed to both macrophage-activating factor and lipopolysaccharide, i.e., conditions leading to complete parasite destruction. The mechanisms of respiratory burst inhibition by intracellular Leishmania spp. are unclear, but these observations suggest that such effects may contribute significantly to intracellular survival of the microorganisms.

摘要

当在体外受到巨噬细胞激活因子或脂多糖刺激时,小鼠腹腔巨噬细胞在受到膜活性试剂触发时会获得产生强烈呼吸爆发的能力。利什曼原虫属(恩氏利什曼原虫、硕大利什曼原虫)的细胞内寄生虫的存在显著抑制了这种活性,这通过化学发光、细胞色素c还原、硝基蓝四氮唑以及磷酸己糖旁路水平来衡量。相反,惰性细胞内颗粒如乳胶珠强烈增强了巨噬细胞的呼吸爆发,这表明与利什曼原虫相关的抑制是由特定的寄生虫效应导致的。细胞内利什曼原虫属对巨噬细胞氧化代谢的损害是感染微生物数量的函数,并且在感染活寄生虫的巨噬细胞中比感染死寄生虫的巨噬细胞中更明显。此外,在同时暴露于巨噬细胞激活因子和脂多糖的恩氏利什曼原虫感染的巨噬细胞中,代谢抑制不太明显,即导致寄生虫完全破坏的条件下。细胞内利什曼原虫属抑制呼吸爆发的机制尚不清楚,但这些观察结果表明,这种效应可能对微生物在细胞内的存活有显著贡献。

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