Division of Infectious Diseases, University of California, San Diego, CA 92103, USA.
Exp Parasitol. 2010 Dec;126(4):617-20. doi: 10.1016/j.exppara.2010.06.007. Epub 2010 Jun 9.
High-throughput drug screening methods against the intracellular stage of Leishmania have been facilitated by the development of in vitro models of infection. The use of cell lines rather than primary cells facilitates these methods. Peripheral blood mononuclear cell (PBMC) derived macrophages and THP-1 cells were infected with stationary phase egfp transfected Leishmania amazonensis parasites and then treated with anti-leishmanial compounds. Drug activity was measured using a flow cytometric approach, and toxicity was assessed using either the MTT assay or trypan blue dye exclusion. Calculated EC(50)'s for amphotericin B, sodium stibogluconate, and miltefosine were 0.1445±0.0005μg/ml, 0.1203±0.018mg/ml, and 26.71μM using THP-1 cells, and 0.179±0.035μg/ml, 0.1948±0.0364mg/ml, and 13.77±10.74μM using PBMC derived macrophages, respectively. We conclude that a flow cytometric approach using egfp transfected Leishmania species can be used to evaluate anti-leishmanial compounds against the amastigote stage of the parasite in THP-1 cells with excellent concordance to human PBMC derived macrophages.
高通量药物筛选方法针对利什曼原虫的细胞内阶段已通过体外感染模型的发展而得到促进。细胞系的使用而不是原代细胞促进了这些方法。静止期 egfp 转染的利什曼原虫 amazonensis 寄生虫感染外周血单核细胞(PBMC)衍生的巨噬细胞和 THP-1 细胞,然后用抗利什曼化合物处理。使用流式细胞术方法测量药物活性,并使用 MTT 测定法或台盼蓝染料排除法评估毒性。使用 THP-1 细胞计算两性霉素 B、葡萄糖酸锑钠和米替福新的 EC(50) 分别为 0.1445±0.0005μg/ml、0.1203±0.018mg/ml 和 26.71μM,使用 PBMC 衍生的巨噬细胞计算 EC(50) 分别为 0.179±0.035μg/ml、0.1948±0.0364mg/ml 和 13.77±10.74μM。我们得出结论,使用 egfp 转染的利什曼物种的流式细胞术方法可用于评估抗利什曼化合物对寄生虫的无鞭毛体阶段在 THP-1 细胞中的活性,与人类 PBMC 衍生的巨噬细胞具有极好的一致性。