Apical cytoplasm

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

Localization of diamine oxidase and d-amino acid oxidase in kidney, demonstrated by means of immunohistochemical method

Abstract: The localization of both diamine oxidase and D-amino acid oxidase was examined by immunofluorescent technique on the frozen section of the porcine kidneyThe cells, composing the Bowman's capsule and the proximal convoluted tubule, showed intense fluorescence which showed the localization of diamine oxidase The antigen was concentrated in the supra- and para-nuclear cytoplasm But, unlike monoamine oxidase, diamine oxidase may not be located in the mitochondria, because higher concentration of diamine oxidase is found in the apical cytoplasm where the mitochondria are not so much observedThe D-amino acid oxidase was demonstrated in the apical cytoplasm of the cells constituting the Bowman's capsule, the proximal convoluted tubule and a part of the Henle's loopThe place where two enzymes were located was, as mentioned above, mostly in the proximal convoluted tubule At this place, the large amount of ammonia was reported to be secreted and the highest activity of the two enzymes was also encountered In other words, the location of two enzyme proteins, the place where ammonia is eliminated and the sites of enzymatic activity of two enzymes were quite identical

Electron microscopic identification of the colorectal origins of tumor cells in pleural fluid.

Abstract: Cellular material from metastatic rectal and lung adenocarcinomas was recovered from pleural and pericardial fluids, respectively. It was examined by electron microscopy (EM) to determine if certain ultrastructural features, which are primarily prominent in colorectal adenocarcinomas, were maintained in the tumor cells in metastatic fluid. These features include the presence of microvilli with dense microfilamentous cores that extend deeply into the apical cytoplasm (cytoplasmic rootlets) and an abundance of glycocalyceal bodies. It was found that tumor cells from the patient with a primary rectal adenocarcinoma exhibited these critical distinguishing characteristics. The cells from the lung adenocarcinoma, while containing many well-developed microvilli, did not possess cytoplasmic rootlets or glycocalyceal bodies. In addition, and possibly of more diagnostic significance, is the observation that the presence of microvilli and cytoplasmic rootlets remained evident in tissue pieces and cell blocks initially processed in paraffin and then reembedded for EM.

Fine structural analysis of the effect of trypan blue on the visceral endoderm of the mouse egg cylinder.

Abstract: The effects of a maternal injection of trypan blue on primitive streak mouse embryos were studied with electron microscopy. Commercial trypan blue was purified by descending paper chromatography, and pregnant females received an intraperitoneal injection of the collected blue fraction on the evening of the 7th day of gestation. Ultrastructurally, the changes in the visceral endoderm were apparent 10 min after the injection and included an increase in the number of fuzzy-coated vesicles in the apical cytoplasm. By 20 min the apical cytoplasm of the extraembryonic visceral endodermal cells was filled with many fuzzy-coated vesicles and numerous vacuoles of various size and electron density. 30 min after the injection, the extraembryonic visceral endodermal cells were relatively smooth lacking a microvillous border and evidence of endocytic activity was rare. Many embryonic visceral endodermal cells were observed in various stages of degeneration although the underlying embryonic ectoderm appeared unaffected. Morphologically, it appears that trypan blue exerts its first effect by altering the endocytic activity of the visceral endoderm.

Vas Deferens Surface Epithelium of Agouti paca: Fine Structural Features Epitelio del Conducto Deferente de Agouti paca. Observaciones de Estructura Fina

Abstract: SUMMARY: The surface epithelium of the vas deferens of Agouti paca, a wild and large South American rodent, was basically formed by principal and basal cells being only the principal cells related to endocytosis processes and also secretion taking base on their cytoplasmic ultrastructural features. Principal cell of vas deferens epithelium were characterized mainly by presence of vesicles with several shapes, sizes and internalized content at their apical cytoplasm occurring smaller pits and pale small vesicles seen next to the apical brush border of microvillus. Moreover, coated vesicles, smooth surface vesicles and great vesicles; multivesicular bodies, endosomes and lysosomes were seen. Presence of an apocrine secretory apparatus was also viewed, showing apical cytoplasmic expansions protruding into the vas deferens luminal compartment. The basal flattened cells, without luminal surface contact, occurred next to the basement membrane of the ductus, and did no exhibit special ultrastructural features.

Ultrastructural cytochemical identification of the siderophilic enterocyte.

Abstract: Specific iron-binding sites in the gut were visualized by the sequential incubation of glutaraldehyde-fixed specimens in iron nitrilotriacetate (FeNTA) and acid ferro-cyanide (AF). In rat duodenum, jejunum, and ileum, approximately half of the enterocytes from the crypt to the distal villus contained FeNTA-AF-reactive material. The staining intensity of individual enterocytes appeared to decrease progressively in more distal locations in the gut. Maximal FeNTA-AF staining was observed in cells in the upper half of the villus, and was localized primarily in microvilli, apical cytoplasm, and lateral membranes. In duodenal crypt cells, stain deposits were present primarily in the microvilli. FeNTA-AF stained sites in the cytoplasmic and microvillus matrix were approximately 100-fold greater in number than were sites of intrinsic iron stained with AF alone. FeNTA-AF and AF staining in human duodenal enterocytes was similar to that observed in rat duodena, demonstrating the applicability of this methodology to human samples. In rat duodena, the distribution of AF staining alone in specimens taken 10 min after the in vivo intraduodenal administration of FeCl2 was similar to that of FeNTA-AF staining in tissue from fasted animals not given iron. The distribution and frequency of iron-binding sites stainable with the FeNTA-AF method which occur in a subpopulation of enterocytes can be correlated closely with physiologic, histologic, and ultrastructural parameters of inorganic iron absorption previously reported.