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Development of the distal end and Tomes' processes of

ameloblasts observed by freeze-fracture and ultrathin section


electron microscopy.
D L Franklin, N J Severs, and E Katchburian

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Abstract
A freeze-fracture examination of distal portions of differentiating and secretory ameloblasts was
carried out using upper molar tooth germs from one to four days old rats. Ultrathin sections were
prepared for comparison. Freeze-fracture provides a unique opportunity to observe plasma
membrane events in distal portions of ameloblasts during differentiation and development. Our
results suggest that the distal plasma membrane and Tomes' processes of differentiating and
secretory ameloblasts are highly active in endocytosis. In differentiating ameloblasts, endocytic
activity is likely to be associated with removal of the basal lamina. During matrix secretion and
maturation, ameloblasts are probably removing material from the maturing matrix; in particular
amelogenins and water. The present study provides morphological evidence that an endosomal
system is present in differentiating and secretory ameloblasts during periods of endocytic
activity. This would provide a system whereby ligands, fluid components, membrane receptors
and plasma membrane, which enter the cells during endocytosis, may be separated from each
other and sorted out for despatch to different destinations.

Selected References

These references are in PubMed. This may not be the complete list of references from
this article.

 FEARNHEAD RW. Mineralization of rat enamel. Nature. 1960 Nov 5;188:509–


510. [PubMed] [Google Scholar]
 Hasty DL. Freeze-fracture studies of neonatal mouse incisors. Anat Rec. 1983 Apr;205(4):405–
420. [PubMed] [Google Scholar]
 Helenius A, Kartenbeck J, Simons K, Fries E. On the entry of Semliki forest virus into BHK-21
cells. J Cell Biol. 1980 Feb;84(2):404–420. [PMC free article] [PubMed] [Google Scholar]
 Herold R, Christner P, Graver H, Rosenbloom J. Immunofluorescent evidence for the similarity of
amelogenins in calf, mouse and pig teeth. J Dent Res. 1979 Mar;58(SPEC):992–
993. [PubMed] [Google Scholar]
 Hubbard AL. Endocytosis. Curr Opin Cell Biol. 1989 Aug;1(4):675–683. [PubMed] [Google
Scholar]
 Kallenbach E. Fate of horseradish peroxidase in the secretion zone of the rat incisor enamel
organ. Tissue Cell. 1980;12(3):491–501. [PubMed] [Google Scholar]
 Katchburian E, Burgess AM. Lysosomes and removal of the basal lamina of ameloblasts in early
stages of odontogenesis. Cell Biol Int Rep. 1983 Jun;7(6):407–415. [PubMed] [Google Scholar]
 Katchburian E, Holt SJ. Role of lysosomes in amelogenesis. Nature. 1969 Sep
27;223(5213):1367–1368. [PubMed] [Google Scholar]
 Katchburian E, Holt SJ. Studies on the development of ameloblasts. I. Fine structure. J Cell
Sci. 1972 Sep;11(2):415–447. [PubMed] [Google Scholar]
 Leblond CP, Warshawsky H. Dynamics of enamel formation in the rat incisor tooth. J Dent
Res. 1979 Mar;58(SPEC):950–975. [PubMed] [Google Scholar]
 Reith EJ. The early stage of amelogenesis as observed in molar teeth of young rats. J Ultrastruct
Res. 1967 Mar;17(5):503–526. [PubMed] [Google Scholar]
 Robinson C, Kirkham J, Briggs HD, Atkinson PJ. Enamel proteins: from secretion to maturation. J
Dent Res. 1982 Dec;Spec No:1490–1495. [PubMed] [Google Scholar]
 Robinson C, Briggs HD, Atkinson PJ, Weatherell JA. Matrix and mineral changes in developing
enamel. J Dent Res. 1979 Mar;58(SPEC):871–882. [PubMed] [Google Scholar]
 Robinson C, Briggs HD, Kirkham J, Atkinson PJ. Changes in the protein components of rat incisor
enamel during tooth development. Arch Oral Biol. 1983;28(11):993–1000. [PubMed] [Google
Scholar]
 Sasaki T. Tracer, cytochemical, and freeze-fracture study on the mechanisms whereby secretory
ameloblasts absorb exogeneous proteins. Acta Anat (Basel) 1984;118(1):23–
33. [PubMed] [Google Scholar]
 Sasaki T, Motegi N, Higashi S. Morphological analysis of the Golgi apparatus in rat amelogenesis
as revealed by the Ur-Pb-Cu block staining method and freeze-fracture replication. J Electron
Microsc (Tokyo) 1984;33(1):19–33. [PubMed] [Google Scholar]
 Sasaki T, Nakagawa K, Higashi S. Fine structure of secretory ameloblasts in kitten tooth germs,
with special regard to intercellular junctions as revealed by freeze-fracture. Arch Oral
Biol. 1983;28(2):177–183. [PubMed] [Google Scholar]
 Slavkin HC, Mino W, Bringas P., Jr The biosynthesis and secretion of precursor enamel protein by
ameloblasts as visualized by autoradiography after tryptophan administration. Anat Rec. 1976
Jul;185(3):289–312. [PubMed] [Google Scholar]
 Steinman RM, Brodie SE, Cohn ZA. Membrane flow during pinocytosis. A stereologic analysis. J
Cell Biol. 1976 Mar;68(3):665–687. [PMC free article] [PubMed] [Google Scholar]
 Termine JD, Belcourt AB, Christner PJ, Conn KM, Nylen MU. Properties of dissociatively
extracted fetal tooth matrix proteins. I. Principal molecular species in developing bovine
enamel. J Biol Chem. 1980 Oct 25;255(20):9760–9768. [PubMed] [Google Scholar]
 Warren G, Woodman P, Pypaert M, Smythe E. Cell-free assays and the mechanism of receptor-
mediated endocytosis. Trends Biochem Sci. 1988 Dec;13(12):462–465. [PubMed] [Google
Scholar]
 Warshawsky H. A freeze-fracture study of the topographic relationship between inner enamel-
secretory ameloblasts in the rat incisor. Am J Anat. 1978 Jun;152(2):153–207. [PubMed] [Google
Scholar]
 Weinstock A, Leblond CP. Elaboration of the matrix glycoprotein of enamel by the secretory
ameloblasts of the rat incisor as revealed by radioautography after galactose- 3 H injection. J Cell
Biol. 1971 Oct;51(1):26–51. [PMC free article] [PubMed] [Google Scholar]

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