| Abstrakt: |
This scanning electron microscope (SEM) study of secretory- and transitional stage enamel organ, cells of the permanent dentition of Macaca mulatta and Macaca arctoides was undertaken because the topography of these cell in primates has not been described in the literature Comparison of our results with murine enamel organ morphology Reported previously revealed not only similarities, but also some significant differences. Tooth buds of the permanent dentition were routinely prepared /or SEAM Murine secretoy stage amneloblasts have been described to be 65-70 µm long with smooth lateral membranes, but those of monkeys were only 30-35µm tall, with four different lateral plasma membrane configuration: smooth, filamentous form was most common. Cells were seen with either transverse or longitudinal ridges in the basal half, and with filamentous ridges in the apical portion; this indicated modulation between these form. Because of the extraordinary similarity between these lateral membrane modulations and those of rat incisor-maturation ameloblasts, a comparable function is proposed -- namely, that monkey secretory ameloblasts function, in part, in the resorption and mineralization of enamel matrix. There were several layers of rounded stratum intermedium cells basal to monkey secretory-stage ameloblasts, bat only one layer of cuboidal stratum intermedium in rodents. The stellate reticulum cells of rats and monkeys appeared attenuated, with large extracellular spaces-There was little or no reduction in cell length of monkey transitional-stage ameloblasts. The position of the nuclear bulge differentiated transitional- from secretory-stage umeloblasts. The lateral surfaces of monkey transitional ameloblasts had interdigitaling bulbous extensions of cytoplasm, whereas those of mice were smooth, and became microvillous late in the transition stage. In this stage, monkey and murine stratum intermedium, stellate reticulum, and the outer enamel epithelium cells changed morphology to become papillary cells with microvillous surfaces. Clusters of papillary cells were separated from each other by anastomosing blood vessels, with diameters ranging from 10 to 12 µm in monkeys, but from only 5 to S µm in murine incisor teeth. [ABSTRACT FROM AUTHOR] |
