Benítez Diego, Medeiros Andrea, Quiroga Cristina, Comini Marcelo A
Group Redox Biology of Trypanosomes, Institut Pasteur de Montevideo, Montevideo, Uruguay.
Departamento de Bioquímica, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay.
Methods Mol Biol. 2022;2524:127-147. doi: 10.1007/978-1-0716-2453-1_10.
This chapter describes a viability assay for the intracellular (amastigote) and clinically relevant form of Leishmania infantum that is based on the detection of bioluminescence (BL) signal. The assay uses a reporter cell line of L. infantum that expresses constitutively a redshifted luciferase from Photinus pyralis and murine macrophages (cell line J774.A1) as host cells for infection. The host cell line was selected because it is a differentiated cell line, easy to manipulate in vitro, and advantageous for ethical reasons. This chapter introduces an assay designed for the screening of bioactive compounds/molecules employing a 96-well microplate and a 24 h treatment. The assay setup shows excellent balance between simplicity (cell culture manipulation/infection and timing) and quality parameters, as well as potential to detect drug-like molecules acting in a fast and cytotoxic manner.
本章介绍了一种针对婴儿利什曼原虫细胞内(无鞭毛体)且具有临床相关性形式的活力测定方法,该方法基于生物发光(BL)信号的检测。该测定使用了一种婴儿利什曼原虫的报告细胞系,其组成性表达来自萤火虫的红移荧光素酶,并使用鼠巨噬细胞(细胞系J774.A1)作为感染的宿主细胞。选择该宿主细胞系是因为它是一种分化细胞系,易于在体外操作,且出于伦理原因具有优势。本章介绍了一种使用96孔微孔板和24小时处理来筛选生物活性化合物/分子的测定方法。该测定设置在简单性(细胞培养操作/感染和时间安排)和质量参数之间表现出出色的平衡,以及检测以快速且具有细胞毒性方式起作用的类药物分子的潜力。