Literature DB >> 978131

Effect of ascorbic acid deficiency on mouse second molar tooth germs cultivated in vitro.

G E Levenson.   

Abstract

Mandibular second molar tooth germs from two-day old mice were cultured in vitro, on millipore membranes, for periods of up to 20 days in liquid medium with or without added ascorbic acid. Tooth germs grown in ascorbate medium were characterized by relatively normal growth, differentiation, morphology and histology. Cuspation patterns were maintained. The epithelial root sheath continued to grow along the millipore membrane. Tooth germs cultured in ascorbate-deficient medium manifested a consistent and striking failure in maintenance of differentiated odontoblastic and ameloblastic tissue with arrest of predentin synthesis, severe structural collapse and reduction in size. Cuspation patterns were lost in scorbutic molars, with sinking of surface layers into pulpal tissue and flattening of the entire organ. This resulted in a lack of recognizable morphology and in severe disorganization of tissues. Only growing areas of the root sheath with associated proliferation of preameloblasts and pre-odontoblasts and adjacent pulpal tissue remained normal and refractory to ascorbate deficiency. Odontoblastic as well as ameloblastic layers were disrupted and cells were dedifferentiated. Newly differentiated odontoblasts became highly vacuolated when they became polarized and started to secrete extracellular matrix.

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Year:  1976        PMID: 978131

Source DB:  PubMed          Journal:  J Embryol Exp Morphol        ISSN: 0022-0752


  4 in total

1.  A new culture method assuring the three-dimensional development of the mouse embryonic molar tooth in vitro.

Authors:  Y Sakakura
Journal:  Calcif Tissue Int       Date:  1986-10       Impact factor: 4.333

2.  A simple, disposable, and improved organ culture system for maintaining three-dimensional development of mouse embryonic molars.

Authors:  Y Sakakura; N Fujiwara; T Nawa
Journal:  In Vitro Cell Dev Biol       Date:  1989-10

3.  An ultrastructural study of dentinogenesis and amelogenesis in rat molar tooth germs cultured in vitro.

Authors:  I Gorter de Vries; P C Ameloot; D Coomans; E Wisse
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

4.  Metabolic expression of intrinsic developmental programs for dentine and enamel biomineralization in serumless, chemically-defined, organotypic culture.

Authors:  J Evans; P Bringas; M Nakamura; E Nakamura; V Santos; H C Slavkin
Journal:  Calcif Tissue Int       Date:  1988-04       Impact factor: 4.333

  4 in total

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