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使用部花青540和 Hoechst 33258选择性杀灭细胞培养物中的污染支原体。

Use of Merocyanine 540 and Hoechst 33258 for the selective killing of contaminating mycoplasmas in cell cultures.

作者信息

Tarshis M, Katzenel A, Rottem S

机构信息

Department of Membrane and Ultrastructure Research, Hebrew University - Hadassah Medical School, Jerusalem, Israel.

出版信息

J Immunol Methods. 1994 Feb 10;168(2):245-52. doi: 10.1016/0022-1759(94)90061-2.

Abstract

Mycoplasma infection can substantially affect the biological properties of cells in vitro. We have devised a method for the selective killing of mycoplasmas, e.g., A. laidlawii, M. fermentans, M. hyorhinis and M. arginini, from experimentally infected cell cultures. This approach is based on the differential binding of the lipophilic fluorescent probe Merocyanine 540 followed by illumination with visible light. The efficiency of the procedure depends on the Merocyanine 540 concentration, the intensity of illumination, and the presence of oxygen in the medium. When A. laidlawii contaminated corneal endothelial cell cultures were treated simultaneously with Merocyanine 540 and DNA-binding fluorochrome Hoechst 33258 and then illuminated, a significant degree of eradication was observed, even after one cycle of treatment. This combined treatment is therefore recommended as an effective method of purging mycoplasmas from contaminated cultures.

摘要

支原体感染可在很大程度上影响体外培养细胞的生物学特性。我们设计了一种从实验感染的细胞培养物中选择性杀灭支原体的方法,例如莱氏无胆甾原体、发酵支原体、猪鼻支原体和精氨酸支原体。该方法基于亲脂性荧光探针部花青540的差异结合,随后用可见光照射。该过程的效率取决于部花青540的浓度、光照强度以及培养基中氧气的存在。当用部花青540和DNA结合荧光染料Hoechst 33258同时处理被莱氏无胆甾原体污染的角膜内皮细胞培养物,然后进行光照时,即使在一个处理周期后,也观察到了显著程度的清除。因此,推荐这种联合处理方法作为从污染培养物中清除支原体的有效方法。

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