Casale J M, Rochat T R, Moore K C, Hunninghake G W
Department of Internal Medicine, Veterans Administration, Iowa City, IA.
J Lab Clin Med. 1987 Dec;110(6):767-72.
When type II alveolar cells are maintained in culture, they gradually lose their characteristic lamellar bodies and their ability to secrete surface active material. We evaluated the feasibility of using electron microscopy and stereology to quantitate the effects of multiple culture conditions on the ultrastructure of type II alveolar cells, in vitro. The decrease in lamellar body volume density with time in culture was not affected by culturing the cells in the presence of insulin, fibronectin, or complex extracellular matrix. However, dexamethasone significantly prevented this decrease in lamellar body volume density. The mitochondrial volume density of the cells remained constant with time in culture under control conditions and in the presence of insulin, dexamethasone, or fibronectin. There was, however, a significant increase in mitochondrial volume density, for a short period of time (48 hours), when cells were cultured in the presence of complex extracellular matrix. These studies suggest that electron microscopy with stereology provides an excellent technique to quantitate in vitro ultrastructural changes in cultured type II alveolar cells.
当Ⅱ型肺泡细胞在培养中维持时,它们会逐渐失去其特征性板层小体以及分泌表面活性物质的能力。我们评估了使用电子显微镜和体视学来定量多种培养条件对体外Ⅱ型肺泡细胞超微结构影响的可行性。培养过程中板层小体体积密度随时间的降低不受在胰岛素、纤连蛋白或复杂细胞外基质存在下培养细胞的影响。然而,地塞米松显著阻止了板层小体体积密度的这种降低。在对照条件下以及在胰岛素、地塞米松或纤连蛋白存在时,细胞的线粒体体积密度随培养时间保持恒定。然而,当细胞在复杂细胞外基质存在下培养时,线粒体体积密度在短时间内(48小时)有显著增加。这些研究表明,电子显微镜结合体视学为定量培养的Ⅱ型肺泡细胞的体外超微结构变化提供了一种出色的技术。