Roth J
Respir Physiol. 1975 Apr;23(3):325-35. doi: 10.1016/0034-5687(75)90083-3.
For electron microscopic demonstration of complex carbohydrates and simple sugars in the mouse lung, anionic dye and lectins were used. After immersion fixation of small lung tissue blocks, the alveolar surfactant system was destroyed and only membrane bound carbohydrates (cell coat) could be demonstrated by means of colloidal iron and ruthenium red. Fixation of the whole lung via the visceral pleura preserved the alveolar surfactant system. Only this technique afforded a distinction between cell coat components and hypophase components. After performance of the Concanavalin A-peroxidase technique and after incubation in ferritin-labed Concanavalin A, Lens culinaris lectin or Ricinus communis lectin, various saccharide moieties were demonstrable by immune electron microscopy in the hypophase of the alveolar surfactant system.
为了在小鼠肺中对复合碳水化合物和单糖进行电子显微镜显示,使用了阴离子染料和凝集素。对小块肺组织进行浸入固定后,肺泡表面活性物质系统被破坏,只有膜结合碳水化合物(细胞被膜)可以通过胶体铁和钌红显示出来。通过脏胸膜对整个肺进行固定可保留肺泡表面活性物质系统。只有这种技术能够区分细胞被膜成分和液相成分。在进行伴刀豆球蛋白A-过氧化物酶技术以及在铁蛋白标记的伴刀豆球蛋白A、菜豆凝集素或蓖麻凝集素中孵育后,通过免疫电子显微镜可在肺泡表面活性物质系统的液相中显示出各种糖部分。