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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 207 (1983), S. 533-538 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Cross-striations are traditionally associated with the enamel rods in many species including man. Although these striations are obvious with light microscopy, their exact nature has been difficult to determine with the transmission electron microscope on thin sections of enamel. Thin section microscopy either reveals no structures that can be called cross-striations, or shows periodic light and dark bands across the rods. Superficially, these bands resemble chatter artifact. To test this possibility, rat incisor enamel was used because cross-striations have not been demonstrated on these enamel rods. Thin sections were prepared of enamel blocks oriented in various ways with respect to the cutting edge of the diamond knife. The sections showed either uniform enamel or light and dark bands over rod profiles or interrod enamel. Since these bands could be produced artifactually it is concluded that similar bands seen on enamel rods of other species may also be artifacts.
    Additional Material: 4 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 209 (1984), S. 289-295 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The distribution of approaches of rough endoplasmic reticulum to the cell membrane within the supranuclear region of the secretory ameloblast of the rat incisor was quantitated using a Zeiss MOP-3. In ameloblasts cut in cross section, most of these approaches appear as circular profiles representing cross sections of elongated cisternae, which are aligned parallel to the long axis of the cell. Because of their position, orientation, and distribution of ribosomes, these approaches were consistent with the appearance of subsurface cisternae. Using cross-sectioned ameloblasts, the lengths of apposed plasma membranes either between or within rows of cells were measured from electron micrographs. Along these lengths, matched approaches of rough endoplasmic reticulum from opposite sides of the apposed plasma membranes were counted. Approaches from either side that were unmatched were also counted. Thirteen percent of the approaches were matched between rows of ameloblasts, and 13.5% of the approaches were matched within rows, demonstrating no significant difference between the two sites. Furthermore, mathematical analysis showed that the theoretical probability of two approaches coinciding is 17%. The experimental values are not statistically different from the theoretical probability, and it is concluded that the matching of rough endoplasmic reticulum approaches to the plasma membrane, or subsurface cisternae, occurs at random.
    Additional Material: 5 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 207 (1983), S. 1-16 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Enamel crystallites are electron opaque without osmium or heavy metal staining and give a crystalline electron diffraction pattern. Since the opacity and diffraction pattern are abolished from ultrathin sections of young enamel by floating on distilled water (Bishop and Warshawsky, 1982), the possibility that aqueous staining may also remove crystallites was tested. In addition, the effect of osmium postifixation on crystallite structure was examined.Rat incisors fixed by perfusion with a mixture of aldehydes were either nonosmicated or osmicated prior to dehydration. Incisor segments in the region of inner enamel secretion were embedded in the same Epon block to ensure reliable comparison. Osmicated enamel was more intensely stained with toluidine blue and more electron opaque than nonosmicated enamel. No other structural differences were seen. However, crystallites in osmicated enamel were more resistant to grid demineralization and electron beam damage. Routine staining was done by floating sections on solutions of uranyl acetate and lead citrate; sections were also floated on similar solutions from which the heavy metals were omitted. These solutions removed the electron opaque crystallites from the youngest enamel. Stained sections showed electron opaque crystallite-like structure similar to unstained enamel. When sections that were extracted by the solutions from which the metals were omitted were restained, they appeared identical to routinely stained enamel. It was conclud that staining of young enamel removes the crystallites and reveals only the organic matrix.
    Additional Material: 38 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 232 (1992), S. 325-339 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Zinc iodide-osmium tetroxide (ZIO) is a nonspecific but selective impregnation method that visualizes a tubulo-vesicular system in cells. The detailed structure and three-dimensional distribution of this ZIO-impregnated system was studied in the Tomes' process of secretory ameloblasts in the rat incisor. The ZIO-impregnated system consisted of an extensive array of smooth membranebound thick and thin tubules and vesicles. The interconnected thick and thin tubules formed a complex “core network” in the central cytoplasm of Tomes' process that enmeshed and often surrounded individual secretory granules. From the core network, radial branches extended toward the smooth cell membrane of the interdigitating portion of Tomes' process. Although the core network and branches frequently appeared connected to the secretory granules and the cell membrane, stereo-pair electron microscopy failed to show conclusive evidence of such continuity. However, many coated vesiclelike structures were attached to the core network and its branches. No special relationship was found between interrod and rod secretory sites and the tubulo-vesicular network. In thick sections, the ZIO-impregnated tubulo-vesicular network occupied a considerable volume of cytoplasm. The vinblastine-labile nature of this network as demonstrated previously (Nanci et al., 1987) indicated that the system undergoes rapid and extensive turnover. Considering the dynamic nature and sheer volume of the tubulo-vesicular system, we propose that it be regarded as a major cell organelle.
    Additional Material: 14 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 161 (1968), S. 211-229 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The fine structure of the ameloblasts which secrete the inner enamel matrix in rat incisors was described using light and electron microscopy. The tissue was fixed by perfusion with 2.5% glutaraldehyde and gently decalcified in isotonic EDTA.The ameloblasts are tall cells forming a simple columnar epithelium. The base is adjacent to the stratum intermedium and the apex (Tomes' process) extends into newly-formed enamel. The infranuclear zone is divided by the basal cell web into a small basal bulge adjacent to the stratum intermedium, and a larger compartment containing most of the cell's mitochondria. The supranuclear zone contains the rough endoplasmic reticulum and the Golgi apparatus. The rough endoplasmic reticulum predominates in the proximal and distal regions of this zone where it occupies most of the cell width. In the intermediate region, the rough endoplasmic reticulum surrounds a central tubule-shaped Golgi apparatus, the tubule wall being made up of flattened saccules. The Golgi region of ameloblasts is associated with coated vesicles, two types of granules (light and dark) which may be lysosomes, and a characteristic dense content granule shown to be the enamel precursor (0.16 μ diameter).The supranuclear zone is separated from Tomes' process by the apical cell web. Tomes' process is devoid of endoplasmic reticulum and Golgi material, but contains numerous dense content granules as well as microtubules and coated vesicles. The amorphous dense content granules are the precursors of the highly orientated fibrous enamel matrix. The proximity of the process to the fibrous enamel suggests that it is involved in orientation of these fibrils. Since bundles of fibrils constitute rods, the process would seem also to be involved in enamel rod orientation.
    Additional Material: 19 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 183 (1975), S. 523-561 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Renewal of the cell populations of the incisor was studied in 100 gm male rats injected with a single dose of 3H-thymidine and sacrificed at various times from one hour to 32 days after injection. Radioautographs showed that a cohort of labeled cells within the enamel organ, odontoblast layer, and pulp was carried passively with the erupting incisor from the apical end toward the gingival margin where the life cycle of these cells was terminated. Labeled cells in the upper and lower incisor, although traversing different absolute lengths, were found in approximately the same functional stage of their life cycle at similar times after the injection. Thus, by one and one-half days labeled ameloblasts began inner enamel secretion. By 32 days labeled ameloblasts had traversed the entire maturation zone and were located at the gingival margin. Labeled odontoblasts followed closely the movement of labeled ameloblast. The mean rate of ameloblast migration was 567 μm/day on the upper incisor and 651 μm/day on the lower. For the odontoblasts this rate was 500 μm/day (upper) and 631 μm/day (lower). Finally, it was found that as the rat aged, the duration of the life cycle for epithelial and pulp cell populations of the incisor increased because of growth within the longitudinal axis of the tooth. It was concluded that the apical end of the incisor literally “grows backward” in the bony socket, and hence, the duration of the life cycle becomes greater simply because it takes cells longer to physically reach the gingival margin.
    Additional Material: 4 Tab.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 188 (1977), S. 143-171 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Presecretory ameloblasts were compared morphologically and functionally to secretory ameloblasts in the rat incisor. Structurally, the cell types are similar except for the absence of a Tomes' process at the presecretory stage. The developmental changes at the apical end of the ameloblast were described and correlated sequentially with the onset of extracellular events. First, a layer a amorphous dense material appeared at the dentinal surface adjacent to the ameloblasts. Second, the initial layer of enamel began to develop. Third, inner enamel secretion began with the appearance of interrod enamel. This occurred concomitantly with the appearance of the interdigitating portions of Tomes' processes.Functionally, the protein synthetic activity of presecretory ameloblasts was compared to secretory ameloblasts. Light microscopic radioautography of 1-m̈m thick Epon sections was used to localize 3H-proline and 3H-tyrosine at various times after injection. At time intervals up to 20 minutes the two presursors were localized as a band of labeled protein in the supranuclear cytoplasm of both presecretory and secretory ameloblasts. At 30 minutes an additional band of radioactivity was localized within the apices of both types of ameloblasts. In presecretory cells the apical reaction band was over the proximal portion of Tomes' processes which border on the dentin. In the secretory cells, the apical reaction band was over both proximal and interdigitating portions of Tomes' processes and over the enamel. Grain counts over the secretory ameloblasts showed that the incorporation of tyrosine increased by 7.5% as opposed to a 63% increase with proline when compared to the values in presecretory cells. The different increases with the two precursors were in keeping with the different amounts of the two amino acids reported to be present in enamel protein.It was concluded that while the secretory ameloblasts synthesize and secrete enamel protein, both presecretory and secretory cell types produce another category of protein which is involved in the apical reaction band. It was proposed that this material is structural protein being contributed to the continuously lengthening Tomes' process which is speculated to occur during formation of enamel.
    Additional Material: 19 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 200 (1981), S. 371-399 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The rat incisor is an excellent model system in which to study amelogenesis. However, the information obtained has not been extrapolated to the human because of alleged structural differences between the teeth. The obvious differences include continuous eruption in rat incisors and an enamel rod pattern in rats which seemingly differs from the keyhole pattern of human enamel. A comprehensive analysis was made of those features of enamel structure considered fundamental to the understanding of its formation. This was done by applying the knowledge of amelogenesis obtained in rat incisors to the teeth of monkey and man. The following points of basic similarity were established between these species: (1) Interrod enamel is secreted first. It forms the side walls of cavities which are initially occupied by Tomes' processes. (2) The formation of interrod cavities is followed by deposition of enamel rods within these spaces. (3) The rods conform to the shape of the cavities and are secreted from one surface of Tomes' process. (4) At the initial site of rod deposition its enamel is continuous with the interrod enamel wall. (5) Growth of the rod compresses the process to one side of the cavity resulting in an arcade-shaped “space” between the rod and the remaining interrod walls. This study demonstrates that it is no longer necessary to postulate a keyhole structure for primate enamel, and it has established that a fundamental similarity exists in the basic structure and in the mode of formation of enamel in all three species.
    Additional Material: 37 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 202 (1982), S. 177-186 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Newly formed rat incisor enamel was fixed aqueously by perfusion with glutaraldehyde and anhydrously by immersion in ethylene glycol. Ultrathin sections were studied using transmission electron microscopy and electron diffraction. Aqueously processed enamel was shown to lose its mineral content when sectioned on distilled water. This mineral loss was minimized by limiting the exposure of sections to the water. In such preparations, enamel crystallites were seen by virtue of their intrinsic electron density only. Selected area electron diffraction provided corroborative evidence for the presence or absence of crystallites in the sections. Observations on mineralized sections and on stained mineralized and distilled-water-demineralized sections revealed organic material apparently in the same location as the crystallites. Anhydrously processed enamel which was sectioned on ethylene glycol showed a similar appearance of the crystallites. This appearance was not obviously altered after staining despite evidence that organelles in the ameloblasts were stained. In view of the observations that both methods yielded similar crystallite morphology, it was concluded that aqueous techniques can be used to study the relationship between organic and inorganic components. However, valid description of crystallites in such preparations requires minimal exposure of ultrathin sections to water.
    Additional Material: 19 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 208 (1984), S. 15-31 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Extracellular accumulation of a granular material that is presumed to be an organic “precursor” to mineralized enamel has been reported. This material, generally referred to as “stippled material,” was observed mainly after immersion fixation with osmium tetroxide. In studies with perfusion fixation, the presence of stippled material was inconsistent. Therefore, it appeared that the occurrence of stippled material was dependent on the method of fixation. To test this assumption, tissues were fixed by immersion in either osmium tetroxide or glutaraldehyde and by perfusion with either glutaraldehyde or a mixture of acrolein, glutaradehyde, and formaldehyde. It was found that as the quality of cellular preservation improved, the occurrence of stippled material decreased. Since no stippled material could be found in material judged to be well fixed, it was concluded that stippled material is not an extracellular precursor to mineralized enamel, but is a breakdown product resulting from poor fixation.
    Additional Material: 22 Ill.
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