Further data on intracellular structures of human salivary glands. A SEM study

Specimens of human salivary glands have been studied by our modification of the AODO maceration method which, carried out on sections of controlled thickness, allows the analytical study of human bioptical material. Lately, our technique has been further improved and simplified by omitting the treatment with dimethylsulfoxide and by using osmium-ferrocyanide as secondary fixative. Following maceration with diluted OsO4, some of the sections also were shaken for 10-15 min with a rotating agitator. Already at low magnification, all parenchymal cells were clearly distinguishable for their complement of cytoplasmic organelles. Serous cells and mucous cells at the beginning of their secretory cycle were characterized by well developed RER and Golgi apparatus, while mature mucous cells exhibited only scanty organelles compressed among the secretory droplets. Mitochondria were tubular, and often branched and convoluted. When sectioned, these organelles, besides the usual plate-like cristae, showed tubular cristae as well. The SER of striated and excretory duct cells was well developed and consisted of a network of smooth anastomosing tubules in the apical cytoplasm where it probably represented the transcellular pathway for ion transport. In specimens subjected to shaking, cytoplasmic organelles were occasionally removed allowing a nonobstructed view of the inner side of the plasmalemma and its specializations. With this technique the intercellular canaliculi of serous cells also became appreciable from their cytoplasmic side. They appeared as ribbon-like irregular protrusions with walls fenestrated by holes, corresponding to the interior of microvilli deprived of the cytoskeleton, and, sometimes, with lateral expansions possibly related to the mechanism of exocytosis. Results reported here clearly showed the usefulness of the maceration method in providing additional data on the cytoarchitecture of epithelial cells of salivary glands. Furthermore, by allowing the visualization of internal surfaces previously hidden to direct inspection, our technique may open new horizons in morpho/functional studies of human salivary glands.