首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Photodynamic Sensitization of Leishmania amazonensis in both Extracellular and Intracellular Stages with Aluminum Phthalocyanine Chloride for Photolysis In Vitro
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Photodynamic Sensitization of Leishmania amazonensis in both Extracellular and Intracellular Stages with Aluminum Phthalocyanine Chloride for Photolysis In Vitro

机译:酞菁铝氯化铝对利什曼原虫在细胞外和细胞内阶段的光动力敏化作用

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摘要

Leishmania amazonensis, a causative agent of cutaneous leishmaniasis, is susceptible in vitro to light-mediated cytolysis in the presence of or after pretreatment with the photosensitizer aluminum phthalocyanine chloride. Cytolysis of both promastigotes and axenic amastigotes required less photosensitizer (e.g., one μg · ml−1) and a lower light dose (e.g., 1.5 J · cm−2) than did the mammalian cells examined for comparison. Exposure of Leishmania cells to the photosensitizer alone had little effect on their viability, as judged from their motility, growth, and/or retention of green fluorescent proteins genetically engineered for episomal expression. Fluorimetric assays for cell-associated and released green fluorescence proteins proved to be even more sensitive for the evaluation of cell viability than microscopy for the evaluation of motility and/or integrity. Axenic amastigotes pretreated with the photosensitizer infected macrophages of the J774 line but were lysed intracellularly when the infected cells were exposed to light. Addition of the photosensitizer to the already infected cells produced no effect on their intracellular parasites. However, light irradiation lysed these macrophages and also those infected with parasites preincubated with the photosensitizer at a concentration of 5 μg · ml−1 or higher. Photosensitized Leishmania cells are highly susceptible to cytolysis, apparently due to the generation of reactive oxidative species on light illumination, suggestive of inefficiency of their antioxidant mechanisms. Efficient delivery of photosensitizers to intracellular Leishmania is expected to increase their therapeutic potentials against leishmaniasis.
机译:亚马逊利什曼原虫(Leishmania amazonensis)是皮肤利什曼原虫病的病原体,在光敏剂氯化铝酞菁铝存在下或预处理后,体外易受光介导的细胞溶解作用。与前鞭毛体和轴突吻合动物的细胞溶解相比,需要更少的光敏剂(例如1μg·ml -1 )和更低的光剂量(例如1.5 J·cm −2 )检查了哺乳动物细胞以进行比较。从利什曼原虫细胞单独暴露于光敏剂中,从其活力,生长和/或基因工程改造为游离表达的绿色荧光蛋白的保留情况来看,其活力几乎没有影响。事实证明,与细胞结合和释放的绿色荧光蛋白相比,荧光测定对细胞活力的评估甚至比显微镜对活力和/或完整性的评估更为灵敏。用光敏剂感染的J774系巨噬细胞预处理过的轴突吻合动物,但当被感染的细胞暴露于光线下时,胞内被溶解。向已经感染的细胞中添加光敏剂对其细胞内的寄生虫没有影响。但是,光照射会溶解这些巨噬细胞,以及那些感染了以5μg·ml -1 或更高浓度用光敏剂预孵育的寄生虫的巨噬细胞。光敏利什曼原虫细胞对细胞溶解高度敏感,这显然是由于在光照下会产生反应性氧化物质,这表明其抗氧化机制无效。将光敏剂有效递送至细胞内利什曼原虫预期会增加其抗利什曼原虫病的治疗潜力。

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