Triglia T, Burns G F
J Immunol Methods. 1983 Nov 11;64(1-2):133-9. doi: 10.1016/0022-1759(83)90391-5.
Rapid and reproducible clearance of mycoplasma contaminating human cell lines was achieved using macrophages and antibiotics. Human peripheral blood monocytes were purified by Percoll density gradient centrifugation and allowed to mature into macrophages by 7 days culture in vitro. To the adherent monolayers of macrophages were added the cells to be cleared. Optimal results were obtained with a macrophage to cell concentration of 100:1, together with 200 micrograms/ml of the antibiotics tylosin and lincomycin. The cleared cells were recovered after 7 days of treatment. Monitoring with the Hoechst 33258 stain demonstrated that cells cleared by this method have remained mycoplasma-free for over 6 months. The method is unlikely to cause cell mutation or to introduce mouse viruses and is effective on both adherent and non-adherent cell lines.
使用巨噬细胞和抗生素可实现对污染人细胞系的支原体的快速且可重复清除。人外周血单核细胞通过Percoll密度梯度离心法纯化,并在体外培养7天使其成熟为巨噬细胞。将待清除的细胞添加到巨噬细胞的贴壁单层中。巨噬细胞与细胞的浓度为100:1,并添加200微克/毫升的抗生素泰乐菌素和林可霉素时可获得最佳结果。处理7天后回收清除后的细胞。用Hoechst 33258染色监测表明,用该方法清除的细胞在6个月以上未检测到支原体。该方法不太可能导致细胞突变或引入小鼠病毒,并且对贴壁和非贴壁细胞系均有效。