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Journal of Anatomy logoLink to Journal of Anatomy
. 1997 Jun;190(Pt 4):589–600. doi: 10.1046/j.1469-7580.1997.19040589.x

Fine structure of the cap enameloid and of the dental epithelial cells during enameloid mineralisation and early maturation stages in the tilapia, a teleost

ICHIRO SASAGAWA 1
PMCID: PMC1467643  PMID: 9183681

Abstract

Morphological features of the cap enameloid and dental epithelial cells were investigated by light and transmission electron microscopy during the various stages of enameloid mineralisation and early maturation in the tilapia. The pattern of mineralisation along collagen fibrils in the enameloid differed from that in the dentine. Many matrix vesicles were found in the predentine and in the enameloid, suggesting that they may be involved in the initial mineralisation in both regions. Most of the organic matrix disappeared from the cap enameloid during mineralisation and maturation. The disappearance of the organic matrix could be divided into 2 stages. Initially a fine network-like matrix, which probably consisted of glycosaminoglycans and extended between collagen fibrils, began to disappear. At the same time, fine crystallites and electron-dense, fine granular material covered the collagen fibrils as mineralisation of the enameloid began. In the second stage, the maturation of the enameloid, the collagen fibrils degenerated completely and disappeared from the cap enameloid, being replaced by large numbers of large crystals. At the mineralisation stage, the numbers of lysosomal bodies tended to increase in the inner dental epithelial (IDE) cells, which contained a well developed Golgi apparatus and rough endoplasmic reticulum (rER). At the early stage of maturation, a ruffled border was noted at the distal ends of the IDE cells, which contained many mitochondria and lysosomal bodies, but less rER. These features suggest that the cells actively absorb the organic matrix, which includes collagen fibrils, in the cap enameloid. The outer dental epithelial (ODE) cells were translucent cells that contained well developed labyrinthine canalicular spaces from the onset of the mineralisation stage to the middle stage of maturation. The IDE and ODE cells were clearly involved in the mineralisation of the cap enameloid at the mineralisation and maturation stages.

Keywords: Mineralisation, collagen fibrils, enameloid, tilapia, tooth development

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Selected References

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  1. Garant P. R. Observations on the ultrastructure of the ectodermal component during odontogenesis in Helostoma temmincki. Anat Rec. 1970 Feb;166(2):167–187. doi: 10.1002/ar.1091660206. [DOI] [PubMed] [Google Scholar]
  2. Herold R., Rosenbloom J., Granovsky M. Phylogenetic distribution of enamel proteins: immunohistochemical localization with monoclonal antibodies indicates the evolutionary appearance of enamelins prior to amelogenins. Calcif Tissue Int. 1989 Aug;45(2):88–94. doi: 10.1007/BF02561407. [DOI] [PubMed] [Google Scholar]
  3. Isokawa S., Tsubouchi M., Aoki K., Imai M., Kawai A. Studies on the developing enameloid of a fish (Hoplognathus fasciatus). I. Mineralization pattern of enameloid matrix. J Nihon Univ Sch Dent. 1970 Jun;12(2):43–49. doi: 10.2334/josnusd1959.12.43. [DOI] [PubMed] [Google Scholar]
  4. Kawasaki K., Shimoda S., Fukae M. Histological and biochemical observations of developing enameloid of the Sea Bream. Adv Dent Res. 1987 Dec;1(2):191–195. doi: 10.1177/08959374870010020701. [DOI] [PubMed] [Google Scholar]
  5. Kogaya Y. Histochemical properties of sulfated glycoconjugates in developing enameloid matrix of the fish Polypterus senegalus. Histochemistry. 1989;91(3):185–190. doi: 10.1007/BF00490130. [DOI] [PubMed] [Google Scholar]
  6. Kogaya Y. Sulfated glycoconjugates in amelogenesis. Comparative histochemistry and evolution of ectoderm-derived hard tissues. Prog Histochem Cytochem. 1994;29(1):1–110. [PubMed] [Google Scholar]
  7. Linde A., Goldberg M. Dentinogenesis. Crit Rev Oral Biol Med. 1993;4(5):679–728. doi: 10.1177/10454411930040050301. [DOI] [PubMed] [Google Scholar]
  8. Prostak K. S., Seifert P., Skobe Z. Enameloid formation in two tetraodontiform fish species with high and low fluoride contents in enameloid. Arch Oral Biol. 1993 Dec;38(12):1031–1044. doi: 10.1016/0003-9969(93)90164-h. [DOI] [PubMed] [Google Scholar]
  9. Prostak K., Skobe Z. Ultrastructure of the dental epithelium during enameloid mineralization in a teleost fish, Cichlasoma cyanoguttatum. Arch Oral Biol. 1986;31(2):73–85. doi: 10.1016/0003-9969(86)90030-0. [DOI] [PubMed] [Google Scholar]
  10. Sasagawa I., Ferguson M. W. Fine structure of the organic matrix remaining in the mature cap enameloid in Halichoeres poecilopterus, teleost. Arch Oral Biol. 1990;35(9):765–770. doi: 10.1016/0003-9969(90)90101-f. [DOI] [PubMed] [Google Scholar]
  11. Sasagawa I. Fine structure of tooth germs during the formation of enameloid matrix in Tilapia nilotica, a teleost fish. Arch Oral Biol. 1995 Sep;40(9):801–814. doi: 10.1016/0003-9969(95)00050-y. [DOI] [PubMed] [Google Scholar]
  12. Sasagawa I. The appearance of matrix vesicles and mineralization during tooth development in three teleost fishes with well-developed enameloid and orthodentine. Arch Oral Biol. 1988;33(2):75–86. doi: 10.1016/0003-9969(88)90049-0. [DOI] [PubMed] [Google Scholar]
  13. Shimoda S. [Histogenesis of Sea Bream (Pagrus major) enameloid]. Tsurumi Shigaku. 1989 Jan;15(1):267–284. [PubMed] [Google Scholar]

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