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首页> 外文期刊>Canadian journal of microbiology >MURINE MACROPHAGE ELASTOLYTIC ACTIVITY INDUCED BY ASPERGILLUS FUMIGATUS STRAINS IN VITRO - EVIDENCE OF THE EXPRESSION OF TWO MACROPHAGE-INDUCED PROTEASE GENES
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MURINE MACROPHAGE ELASTOLYTIC ACTIVITY INDUCED BY ASPERGILLUS FUMIGATUS STRAINS IN VITRO - EVIDENCE OF THE EXPRESSION OF TWO MACROPHAGE-INDUCED PROTEASE GENES

机译:烟曲霉菌株诱导的小鼠巨噬细胞弹性蛋白酶活力的体外证实两种巨噬细胞诱导的蛋白酶基因的表达。

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摘要

The interaction between Aspergillus fumigatus conidia and murine macrophages of various origins was investigated. Cocultures were carried out between A. fumigatus strains and freshly isolated murine pulmonary alveolar macrophages or two murine macrophage cell-lines: murine alveolar cell-line MALU and murine astrocytoma cell-line J774. By measuring the variation of elastolytic activity in the coculture supernatants with two elastin substrates, we demonstrated that either viable or fixed A. fumigatus or C. albicans yeasts or nonspecific particles induced significant macrophage elastolytic activity. The effect of A. fumigatus supernatant or the purified A. fumigatus galactomannan suggested also the possible involvement of this polysaccharide in macrophage-protease gene expression, release, and activity in invasive aspergillosis. The effect of inhibitory compounds demonstrated the potential implication of a macrophagic metalloprotease and a macrophagic cysteine protease. RNA analysis allowed us to demonstrate the induction of expression of two macrophagic protease genes in stimulated macrophages. Two distinctive mechanisms appeared to be implicated in macrophage protease induction: nonspecific phagocytosis in the earliest times of the coculture and (or) specific galactomannan recognition after its gradual release by the mycelium. [References: 39]
机译:研究了烟曲霉分生孢子与各种来源的鼠巨噬细胞之间的相互作用。在烟曲霉菌株和新鲜分离的鼠肺泡巨噬细胞或两种鼠巨噬细胞细胞系:鼠肺泡细胞系MALU和鼠星形细胞瘤细胞系J774之间进行共培养。通过测量具有两种弹性蛋白底物的共培养上清液中的弹性活性变化,我们证明了有活力的或固定的烟曲霉或白色念珠菌酵母或非特异性颗粒均诱导了显着的巨噬细胞弹性活性。烟曲霉上清液或纯化的烟曲霉半乳甘露聚糖的作用还表明,这种多糖可能参与了巨噬细胞蛋白酶基因的表达,释放以及侵袭性曲霉病的活动。抑制性化合物的作用证明了巨噬金属蛋白酶和巨噬半胱氨酸蛋白酶的潜在意义。 RNA分析使我们能够证明在刺激的巨噬细胞中诱导了两个巨噬蛋白酶基因的表达。在巨噬细胞蛋白酶诱导中似乎涉及两个独特的机制:在共培养的最早时间中的非特异性吞噬作用和(或)在被菌丝体逐渐释放后的特定半乳甘露聚糖识别。 [参考:39]

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