Willingham M C, Rutherford A V
J Histochem Cytochem. 1984 Apr;32(4):455-60. doi: 10.1177/32.4.6323574.
The preservation and contrast of membranous structures in cultured cells using various postfixation procedures prior to embedding have been investigated. These include routine OsO4, ferrocyanide-reduced OsO4, osmium-thiocarbohydrazide-osmium (OTO), and ferrocyanide-reduced osmium-thiocarbohydrazide-ferrocyanide-reduced osmium (R-OTO). With standard ethanol-Epon dehydration/embedding techniques, a dramatic improvement in both membrane contrast and preservation of bilayer membrane structure was achieved using preembedding OTO in cultured cells. R-OTO yielded similar enhanced preservation and contrast of membranes. Both of these methods also resulted in an increase in the contrast of diaminobenzidine reaction product from horseradish peroxidase activity, and of lipid droplets and lipoprotein particles. However, R-OTO did not cause the same increase in the density of proteinaceous elements as was seen with the OTO method. Ferrocyanide-reduced osmium alone showed significant advantages for quantitation of immunocytochemistry using ferritin labels with bismuth subnitrate counterstain. These methods should have general usefulness for the preservation of lipid-containing structures in cultured cells.
研究了在包埋前使用各种后固定程序对培养细胞中膜结构的保存和对比情况。这些程序包括常规的四氧化锇(OsO4)、亚铁氰化物还原的OsO4、锇-硫代碳酰肼-锇(OTO)以及亚铁氰化物还原的锇-硫代碳酰肼-亚铁氰化物还原的锇(R-OTO)。采用标准的乙醇-环氧树脂脱水/包埋技术,在培养细胞中使用包埋前OTO可显著改善膜的对比度以及双层膜结构的保存情况。R-OTO也能使膜的保存和对比度得到类似的增强。这两种方法还能提高辣根过氧化物酶活性产生的二氨基联苯胺反应产物以及脂滴和脂蛋白颗粒的对比度。然而,R-OTO不会像OTO方法那样使蛋白质成分的密度增加。单独使用亚铁氰化物还原的锇对于使用铁蛋白标记和硝酸铋复染进行免疫细胞化学定量具有显著优势。这些方法对于保存培养细胞中含脂质的结构应具有普遍用途。