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Apical cytoplasm

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


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Journal ArticleDOI
TL;DR: It is proposed that actin-containing projections in oxynticopeptic cells are not organized like intestinal microvilli and that filament formation occurs after stimulation by modulating intracellular pools of filamentous and non-filamentous actin.
Abstract: The contribution of brush border cytoskeletal proteins (actin, villin, fimbrin, and brush border myosin-1) to organization of the cytoskeletal network underlying apical plications of oxynticopeptic cells was examined by immunohistochemical techniques in frozen sections of gastric mucosa from the bullfrog, Rana catesbeiana. Apical localization of F-actin with phalloidin in oxynticopeptic cells inhibited with cimetidine revealed small, punctate domains within the apical cytoplasm that were consistent with the presence of short microvilli revealed by electron microscopy. Localization of F-actin in cells stimulated with forskolin was limited to a wide continuous band of cytoplasm corresponding to the location of numerous long surface folds. Inhibition of protein synthesis with cycloheximide did not prevent acid secretion or formation of actin filaments within surface folds in stimulated oxynticopeptic cells, suggesting that the formation of filaments does not require actin synthesis. Staining of gastric mucosae with fluorescent DNase-1 demonstrated that oxynticopeptic cells possess an unusually large pool of non-filamentous actin. Taken together, these results suggest that actin-filament formation in stimulated cells occurs by polymerization of an existing pool of non-filamentous actin. Localization of antibodies specific for villin and fimbrin revealed that these proteins were present within intestinal absorptive cells and gastric surface and neck cells but were not present within inhibited or stimulated oxynticopeptic cells. Brush border myosin-1, present in intestinal absorptive cells, was not present in gastric epithelium. Thus, we propose that actin-containing projections in oxynticopeptic cells are not organized like intestinal microvilli and that filament formation occurs after stimulation by modulating intracellular pools of filamentous and non-filamentous actin.

10 citations

Journal ArticleDOI
TL;DR: The data suggest that the hamster exposed to different photoperiods can be used as a suitable model to study the relationship between testicular morphology and function in different states of gonadal activity.
Abstract: The distribution pattern of testicular sulphydryloxidase (SOx) immuno-activity was investigated in the djungarian hamster during photoperiodically induced testicular involution and recrudescence. SOx immuno-activity, indicating functional integrity of labelled cells, did not change in pachytene spermatocytes and spermatids as long as these cells were present in the seminiferous epithelium. Its disappearance coincided with the degeneration of spermatocytes in phases IV and V of involution and reappeared during recrudescence, when the first spermatogenic wave had reached the pachytene stage. In tubules at phase VI of involution (showing maximal regression), the apical cytoplasm of Sertoli cells showed immuno-activity. This immuno-activity disappeared during recrudescence prior to the differentiation of pachytene spermatocytes. Changes in SOx immuno-activity resembled those of lactate dehydrogenase-X (LDH-X) in photo-inhibited testes or during puberty, indicating a close functional relationship which still remains to be elucidated. The data suggest that the hamster exposed to different photoperiods can be used as a suitable model to study the relationship between testicular morphology and function in different states of gonadal activity.

10 citations

Journal ArticleDOI
TL;DR: The results confirm and extend earlier observations on a functional link between exocytosis and iodination and show that redistribution of peroxidase as well as newly synthesized protein to the site of iodination might be of importance.

10 citations

Journal ArticleDOI
TL;DR: The postnatal development of Brunner's glands in the opossum has been traced, using 170 specimens divided into 21 groups according to snout-rump length to study the development of pyloric and intestinal glands.
Abstract: The postnatal development of Brunner's glands in the opossum has been traced, using 170 specimens divided into 21 groups according to snout-rump length. The newborn opossum has a well developed small intestine, possessing villi and a differentiated intestinal epithelium with concentrations of PAS-positive material in the apical cytoplasm. The ducts of the glands begin to develop within 24 hours after birth and, as they proliferate, two cell types appear. A tall, columnar cell type lines the excretory duct whereas the intralobular duct system is lined by pyramidal cells. Intralobular ducts undergo differentiation by the 50 mm stage and, after this event, secretory units appear as outgrowths from the intralobular duct system. Development continues into early adulthood. Duodenal glands appear to evaginate simultaneously at localized foci, resulting in the formation of a duodenal sinus between glandular elements. The glands evaginate from the mucosa in the most proximal portion of the duodenum, involving both intestinal and gastric mucosal elements. That portion of mucosa lying between the forming glands is submerged and forms the floor of the duodenal sinus. Excretory duct epithelium often lines the sinus in part. The development of Brunner's glands in the opossum is completely independent both of pyloric and intestinal glands.

10 citations

Journal ArticleDOI
TL;DR: In vitro results indicate that in vitro both odontoblasts and (pre)-ameloblasts are involved in the calcium acquisition necessary for the initial stages of mantle dentin mineralization, and in ameloblasts, there is a calcium gradient in the direction of the mineralization front.
Abstract: The relationship between the distribution of calcium in the cells of the enamel organ and the mineralization process in mantle dentin and enamel was investigated at the ultrastructural level in cultured hamster second maxillary molar tooth germs explanted before the onset of mineralization (bell stage). During the early stages of pre-odontoblast and pre-ameloblast differentiation, pyroantimcnate (PA) reaction product for calcium was observed only in the nuclei. However, an abrupt increase in PA reaction product appeared in the apical cytoplasm of both the pre-odontoblasts and pre-ameloblasts prior to the onset of mantle dentin mineralization. In the pre-dentin, the PA reaction product was localized mainly on the striated collagen fibers. The PA reaction product in the apical poles of these cells increased concomitantly with increasing mantle dentin mineralization. The amounts of PA reaction product along the plasma membranes and in the cytoplasm decreased in the direction of the basal (stratum intermedium...

10 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202112
20205
20195
20188
20175
201615