Taylor-Robinson D, Davies H A, Sarathchandra P, Furr P M
Division of Sexually Transmitted Diseases, Clinical Research Centre, Harrow, Middlesex, UK.
Int J Exp Pathol. 1991 Dec;72(6):705-14.
Mycoplasma fermentans (strain 'incognitus') was incubated with HeLa cells for up to 96 h. After 24 h, mycoplasma organisms were demonstrated intracellularly by immunocytochemistry using mule anti-M. fermentans antiserum and gold labelling on ultrathin sections of both Lowicryl K4M and Araldite-embedded HeLa cells, the latter being treated with hydrogen peroxide. The Araldite-embedded cells were fixed with glutaraldehyde and osmium tetroxide in the presence of ruthenium red to stain the mucopolysaccharide surface components of both the procaryotic and eucaryotic cells. Intracellular localization of some M. fermentans organisms was confirmed by exclusion of ruthenium red from their membranes. Various numbers of mycoplasma organisms were seen per cell and occasionally some were within vacuoles, the membranes of which were also unstained by ruthenium red. The PG18 strain of M. fermentans and a strain of M. hominis were also detected intracellularly using similar methodology and homologous mule or rabbit antisera. The occasional presence of both apparently normal and some denser degenerate mycoplasmas in the same cell may indicate gradual degradation by phagolysosomal digestion.
将发酵支原体(“隐匿株”)与HeLa细胞共孵育长达96小时。24小时后,通过免疫细胞化学方法,使用骡抗发酵支原体抗血清并在Lowicryl K4M和Araldite包埋的HeLa细胞超薄切片上进行金标记,在细胞内检测到支原体生物体,后者用过氧化氢处理。Araldite包埋的细胞在钌红存在下用戊二醛和四氧化锇固定,以染色原核细胞和真核细胞的粘多糖表面成分。通过从其膜中排除钌红,证实了一些发酵支原体生物体的细胞内定位。每个细胞可见不同数量的支原体生物体,偶尔有些在液泡内,其膜也未被钌红染色。使用类似方法和同源骡或兔抗血清,在细胞内也检测到发酵支原体的PG18株和人型支原体菌株。在同一细胞中偶尔同时存在明显正常的和一些较致密的退化支原体,这可能表明通过吞噬溶酶体消化逐渐降解。