Filippenko L N, Erokhin V V, Ivanov V B, Fillipenko V N
Biull Eksp Biol Med. 1981 Jul;92(7):117-20.
A new electron microscopy technique is described for detection of lung surfactant proteins with the copper-containing phthalocyanine dye, procion brilliant blue H5GS. The protein structures were stained concurrently with the fixation during perfusion through the pulmonary artery of a fixative-staining mixture containing glutaric aldehyde and a dye in the kakodilate buffer, pH 5.6-6, and in the course of a subsequent immersion of lung tissue pieces into the same mixture. Then the material was treated with thiosemicarbazide and post-fixed with OsO4. The dye did not penetrate intact cells. The electron-dense products of the histochemical reaction were located inside and on the surface of the surfactant membrane, in the hypophase of the surfactant complex, on the plasmalemma of air-blood barrier cells and in its micropinocytosis vesicles, as well as on the membranes of osmophilic plate-like bodies as their contents egressed into the alveolar lumen.
描述了一种新的电子显微镜技术,用于用含铜酞菁染料(普施安亮蓝H5GS)检测肺表面活性物质蛋白。在通过肺动脉灌注含有戊二醛和染料的固定染色混合物(pH 5.6 - 6的二甲胂酸盐缓冲液)的过程中,以及随后将肺组织块浸入相同混合物的过程中,蛋白质结构在固定的同时被染色。然后材料用硫代氨基脲处理,并用四氧化锇后固定。该染料不会穿透完整的细胞。组织化学反应的电子致密产物位于表面活性物质膜的内部和表面、表面活性物质复合物的亚相中、气血屏障细胞的质膜及其微胞饮小泡中,以及嗜锇板层小体的膜上,当其内容物排入肺泡腔时。