Oral Cells and Tissues. Philias R. Garant
cell body with many long folds of cytoplasm that contact and partly overlap similar cytoplasmic folds from adjacent cells. Desmosomes and gap junctions are formed at points of cell-to-cell contact. These folds of cytoplasm line wide extracellular spaces rich in water-binding glycosaminoglycans.
The soft, jellylike consistency of the enamel organ is due to the hydration of the SR glycosaminoglycans. This property is believed to be important in equalizing pressure generated by cell proliferation and matrix secretion in the dental papilla. It has been suggested that, if external tissue-generated forces at the interface between the preameloblasts and the preodontoblasts are eliminated, the three-dimensional outline of the future dentinoenamel junction, and ultimately the shape of the crown of the tooth, can be molded solely by the forces of cell proliferation in both the IEE and the underlying preodontoblasts of the dental papilla. With the onset of ameloblast differentiation, the formation of a terminal web in the IEE, coupled with the assembly of a basement membrane beneath the IEE, stabilizes the shape of the future dentinoenamel junction.
The cells of the SI form a compact zone, one to two cellular layers deep, between the SR and the IEE (Figs 3-1 and 3-2). The intercellular spaces between the SI cells are relatively narrow, and the adjacent cells are held together by many desmosomes. Large gap junctions are formed with adjacent cells of the IEE. The SI cells contain many mitochondria, a characteristic shared with the distal cytoplasm of secretory ameloblasts.
Fig 3-1 Secretory ameloblasts of the rat incisor tooth. In the secretory stage, ameloblasts are tall columnar cells, characterized by a secretory process (Tomes process [TP]) and an infranuclear concentration of mitochondria (M). (BV) Blood vessels; (N) nucleus; (OEE) outer enamel epithelium; (SI) stratum intermedium.
Fig 3-2 Electron micrograph of the proximal end of secretory ameloblasts (AM) containing a high concentration of mitochondria (M). Cells of the stratum intermedium (SI), stellate reticulum (SR), and outer enamel epithelium (OEE) have not yet formed the papillary layer. Blood vessels (endothelium [E]) lie in close apposition to the OEE. (Original magnification × 1,600.)
Although the exact function of the cells of the SI is not clear, the fact that they contain a rich complement of mitochondria and stain intensely for alkaline phosphatase and adenosine triphosphatase (ATPase), suggests a possible role in ion and water transport. The presence of extensive gap junctions between the cells of the SI and the ameloblasts indicates that the two cell types act in close concert during amelogenesis.
Recent studies have shown that the regulatory activity of the enamel knot is taken up by the SI during cusp formation.1 Growth regulatory signals mediated by Sonic Hedgehog (Shh) are activated in the SI in a wavelike manner from the cusp to cervical zone.
The IEE is a layer of columnar preameloblasts abutting the dental papilla. Organ culture studies of amelogenesis indicate that contact with the dental papilla is required for the expression of enamel protein.2 Although the precise nature of the early instructive signals that originate from the dental papilla have yet to be identified, the permissive effect of the extracellular matrix of the basement membrane is required for initiating expression of amelogenin.3
The region of highest mitotic activity in the IEE is located near the cervical loop portion of the enamel organ.4–6 Stem cells in the cervical loop divide to give rise to an expanding metablast clone of preameloblasts.7,8 The rates of proliferation and differentiation in the blast-metablast populations vary among species, among individual teeth, and among different parts of a given tooth.
Secretion of growth factors by the enamel knot and the dental papilla regulate cell proliferation and growth of the IEE.6,9 Receptors for epidermal growth factor, platelet-derived growth factor, and fibroblast growth factor have been localized by immunohistochemistry in preameloblasts.10 Phospholipase Cγ, a downstream signaling molecule activated by growth factor–receptor interaction, was also demonstrated in preameloblasts. Preameloblasts must exit the cell cycle to begin the process of cytodifferentiation.4
The cytoplasm of the preameloblasts contains many free ribosomes, a small Golgi apparatus, a few cisterns of rough and smooth endoplasmic reticulum, and a small number of mitochondria. Adjacent preameloblasts form gap junctions and desmosomes. A prominent zonula adherens junction with an associated terminal web of cytoplasmic filaments forms in the proximal cytoplasm adjacent to the cells of the SI.11,12 This proximal junctional complex binds and stabilizes the preameloblasts prior to degradation of the underlying basal lamina.
Soon after the deposition of mantle dentin, the odontoblasts express matrix metalloproteinases (MMPs) that begin the digestion of the basement membrane. Preameloblasts subsequently remove basement membrane fragments through phagocytosis.13 Removal of the basement membrane allows the dentin and enamel matrices and their respective mineral phases to come into direct contact. As a result, a strong mechanical bond is formed between the enamel and dentin.
Recent studies using reverse transcription and polymerase chain reaction techniques have shown that immature enamel organ cells exist in a “protodifferentiated” state.14 Preameloblasts of the IEE produce small amounts of enamel matrix protein prior to overt morphodifferentiation as secretory phenotypes.15,16 Some of these proteins traverse the dental lamina and are taken up in odontoblast-coated vesicles.
Although the signal transduction pathways that regulate ameloblast and odontoblast differentiation have yet to be identified, immunohistochemical evidence has shown that cytokine-activated signaling pathways, including protein kinase C activation, are involved in early amelogenesis.17
Structure of Secretion-Stage Ameloblasts
In describing the structure of the ameloblast, the term proximal is used to refer to the end of the cell nearest to the SI, and the term distal is used to identify the secretory end of the cell, next to the enamel (see Fig 3-2). The term apical is also used to describe the secretory pole of ameloblasts.
The structural changes that characterize each of the various stages of ameloblastic activity have been well documented.18–21 The cytoplasm of the mature secretory ameloblast is highly polarized (Figs 3-1 to 3-4). The infranuclear (proximal) cytoplasm contains many mitochondria and a terminal web of cytoplasmic filaments associated with a zonula adherens (see Fig 3-2). Gap junctions are present between the proximal surface of the ameloblast and the overlying cell of the SI.
The supranuclear (distal) cytoplasm, which accounts for more than one half of the total cell volume, is filled with an extensive array of RER cisternae and a well-developed Golgi complex (see Figs 3-4a to 3-4c).18,20,22 Electron microscopic autoradiography and immunocytochemical studies have shown that enamel proteins are synthesized in the RER and glycosylated in the Golgi cisternae prior to being packaged into specific granules (see Figs 3-4a to 3-4c).23–25 Condensing vacuoles derived from the trans-Golgi network mature into smaller, dense-core secretory granules. The newly formed secretory granules are immediately transported