Apical cytoplasm

About: Apical cytoplasm is a research topic. Over the lifetime, 1080 publications have been published within this topic receiving 36131 citations.

Organisation of the epidermal syncytial mosaic in diceratocephala boschmai(temnocephalida : platyhelminthes)

Abstract: The epidermis of Diceratocephala boschmai Baer, 1952 (Temnocephalida : Platyhelminthes) was studied using silver-nitrate staining and electron microscopy. The epidermis consists of six syncytia separated by lateral membranes: the frontal, trunk, stalk, adhesive disc syncytia, and a pair of post-tentacular syncytia. Neighbouring syncytia differ in many characters including (1) the presence or absence of locomotory cilia, (2) the degree of the differentiation of the apical cytoplasm layer, (3) the presence or absence of bundles of cytoskeletal filaments, imaginations of basal membrane and other specialised cytoplasmatic structures, (4) the abundance of hemidesmosomes at the basal membrane, and (5) the abundance and nature of gland ducts penetrating the syncytium. These structural differences reflect functional differences between the syncytia. Thus, multisyncytial organisation of the epidermis may be explained by functional differences between the syncytia. Only between the frontal and trunk syncytia has no apparent ultrastructural difference been found.

The endosome-lysosome system in the absorptive cells of goldfish hindgut

Abstract: The vacuolar system in the absorptive cells of the goldfish hindgut was studied by rapid freeze-substituted and cytochemical techniques. The apical cytoplasm of the absorptive cells contained two types of vacuoles: endosomes and lysosomes. The former were characterized by an absence of acid phosphatase activity, a dot-like distribution of material at the peripheral rim, the labelling of the inner surface with horseradish peroxidase (HRP), and by frequent connections to cytoplasmic tubules (CT), which were also free of acid phosphatase activity. The latter vacuole was preferentially located in the deeper cytoplasm and was characterized by the presence of acid phosphatase activity, an electron-dense interior matrix, a peripheral electron-lucent region (a halo), and by the detachment of HRP from the inner surface. Connections between CTs and these latter vacuoles were rarely seen. In the deeper cytoplasm, fusion between endosomes and lysosomes was sometimes observed. These results suggest that the vacuoles which are associated with CTs are endosomes, but not lysosomes, and that internalized materials are transported through the endosome-lysosome system to a giant food vacuole in the cell.

Electron microscopic observations on the epithelium of ram seminal vesicles.

Abstract: The ultrastructure of the secretory cells of the ram seminal vesicle was studied on material fixed by immersion or by vascular perfusion The signs of apocrine secretion seen after immersion fixation did not appear after perfusion fixation and are therefore interpreted as artefacts Instead, vacuoles with a granule in them were seen Such vacuoles were observed in the Golgi apparatus and in the apical cytoplasm Further indications of merocrine secretion were also found It therefore appears that protein secretion in the ram seminal vesicle follows the typical pattern of serous glands The possibility that fructose is extruded with the protein as the vacuoles open at the luminal cell surface is discussed

Ultrastructure of the perfused rat epididymis: effect of luminal sodium ion concentration.

Abstract: The appearance of the rat epididymal epithelium changed when it was perfused in vivo through the lumen with unphysiologically high sodium ion concentrations; dilatation of intercellular spaces (ICS) at threshold concentrations of 30mM-Na+ in the cauda and about 55mM-Na+ in the corpus was associated with absorption of water from the lumen. Despite the distended ICS, junctional complexes appeared intact, and their integrity was confirmed by the exclusion of luminal horseradish peroxidase (HRP) from the ICS, and by demonstrating that circulating [3H]inulin did not enter the lumen. Smooth ER and lipid droplets in the principal cells of the corpus epididymidis were well maintained, and the preservation of granular ER in principal cells of the cauda epididymidis lent morphological support to the continued secretion of protein in this segment. However, occasional distension or involution of inner Golgi cisternae was evident in principal cells after 3–6 h perfusion. In contrast to multivesicular bodies of principal cells, the apical and basal vacuoles characteristic of clear cells changed in size with different perfusing solutions. When low Na+ concentrations were perfused large translucent vacuoles were frequently found in the apical cytoplasm of clear cells in the corpus and cauda epididymidis, and filled vacuoles became larger and showed a decrease in content density in the cauda epididymidis. These large vacuoles were absent from tissue perfused with high Na+ concentrations. Normal pinocytotic activity of both cell types was demonstrated by perfusing HRP which was taken up by the normal route in principal cells, with some transfer to the Golgi cisternae. By far the most HRP was accumulated in clear cell vacuoles irrespective of the composition of the perfusing solution.