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A R Nagy

Publications and source records attributed to A R Nagy.

5 recordsLinked to original sources

Choroidal endothelial junctions in primates.

Junctional ultrastructure of endothelial cells of the choroid was studied with freeze-fracture electron microscopy. A network of multi-stranded linear aggregates was found on arterial endothelial membrane E faces in association with the apposing arterial membrane P face strands. The complexity of the junctional strands decreased as vessel diameter decreased. The choriocapillaris showed staggered junctional strands exclusively on the membrane P face. Junctions of venules and veins were represented by plasmalemmal folds with sparse intramembrane particles on the P face. Freeze-fracture cytochemistry with the membrane probe, filipin, revealed two dissimilar membrane domains: one, an area of membrane fluidity at the junctional strands; and the other, identified by the incorporation of cholesterol into the membrane lipid bilayer, a stable membrane domain. The latter was present throughout endothelial membranes, but was especially prominent on the rims of fenestrations of the choriocapillaris.

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A freeze-fracture study of the papillary layer of the rat incisor enamel organ.

After tooth enamel has been secreted it undergoes maturation or hardening. This process is mediated by ruffled and smooth-ended ameloblasts and associated papillary layer cells. The cells of the papillary layer are characterized by large numbers of mitochondria, coated vesicles, microvilli, and gap junctions. These features have led numerous investigators to speculate that the papillary layer is an ion-transporting epithelium. We have conducted freeze-fracture studies of the rat papillary layer in order to better characterize the surface features of these cells. The cell membranes of the papillary cells contained large numbers of intramembrane particles of various sizes ranging from 4 to 9 nm in diameter. Gap junctions were present at the cell surface and in the cytoplasm in the form of annular gap junctions. The intramembrane particles or connexons of both types of gap junctions were about 8-9 nm wide and were either packed randomly or present in the so-called 'crystallized' state. At the interface between smooth-ended ameloblasts and papillary layer cells, a well-developed zonula occludens was present along the basal surfaces of the ameloblasts and several large gap junctions were formed between the two cell types. The capillary network associated with the papillary layer was characterized by a thin endothelium containing large numbers of fenestrations.

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A freeze-fracture study of synaptogenesis in the distal retina of larval Xenopus.

Synapse formation between photoreceptor, bipolar and horizontal cells of the larval Xenopus retina was studied by the freeze-fracture technique. Photoreceptors and horizontal cells were joined by ribbon synapses; photoreceptor and bipolar cells by basal junctions. Gap junctions were found between photoreceptors and between horizontal cells. Horizontal cell dendrites invaginated receptor bases before the plasma membrane of either cell showed zones of intramembrane (IMP) particle accumulation. Subsequently the receptor cell began to form a synaptic ridge where P-face IMPs aggregated at a protrusion of the surface membrane. The length of the ridge and the density of its IMPs increased between larval stages 40 and 56. Cross-fractured views of receptor cytoplasm at different larval stages showed that synaptic ribbons and synaptic vesicles developed in conjunction with the ridge. Plasmalemmal deformations suggesting sites of vesicle fusion or uptake were noted adjacent to the apex of the ridge. Horizontal cell dendritic membrane first accumulated P-face IMPs at several small regions; subsequently the IMPs became aligned over a broad membrane area. Both rod- and cone-related horizontal cell dendrites also manifested a loose patch of E-face IMPs which subsequently was transformed into a linear array. Basal junctions were characterized by a P-face IMP aggregate in the photoreceptor membrane and an E-face IMP aggregate in the bipolar cell membrane. Basal junctions appeared suddenly in a mature configuration at larval stage 42.

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Synaptic connections linking cones and horizontal cells in the retina of the pikeperch (Stizostedion vitreum).

Cones and horizontal cells of the pikeperch retina were studied with morphological and physiological techniques. Gap junctions were observed between cone pedicles and basal processes emitted by neighboring cones. Intracellular recordings showed that the light-evoked hyperpolarizing cone response was enhanced by light falling upon neighboring receptors within a radius of 50 microns. We suggest that the network of gap junctions between cones mediates the summative lateral interaction described. Three sub-classes of horizontal cells (H1, H2, H3) send dendrites to cones; H1 and H2 cells appear to contact twin cones, exclusively or preferentially, whereas H3 cells appear to synapse only with single cones. Horizontal cells of the same sub-class are joined by gap junctions between dendrites or at the lateral faces of perikarya. These unions extend over several micron 2 and as seen in transmission electron microscopy consist of patches of close apposition alternating with areas of membrane separation, folding and occasional zonulae adherents. Freeze-fracture profiles of horizontal gap junctions show localized areas of dense particle aggregation on the P-face and pits on the E-face flanked by regions of unspecialized membrane. These morphological findings provide support for the known spatial and color-coding properties of pikeperch horizontal cells.

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