Literature DB >> 6381199

Transferrin is required for early tooth morphogenesis.

A M Partanen, I Thesleff, P Ekblom.   

Abstract

The role of circulating molecules during early tooth morphogenesis was studied in organ cultures of mouse embryonic molar-tooth germs. Special attention was focused on the effect of transferrin and insulin, which are necessary for the growth of most cells in culture. The requirement of serum factors for tooth morphogenesis was shown to diminish as the developmental stage advances from the bud stage in day-13 embryos to the cap stage at day 15. The day-15 teeth underwent morphogenesis and cell differentiation in unsupplemented basal culture medium, but the addition of transferrin (50 micrograms/ml) was necessary for the morphogenesis of day-14 tooth germs. We demonstrated, by using transferrin-depleted serum, that transferrin is also necessary for the morphogenesis of day-13 tooth germs. However, some still-unidentified serum components are also required for the morphogenesis of the bud-stage day-13 teeth. These factors apparently do not include insulin, since it was shown to inhibit tooth development. Analysis of the DNA content of tooth germs cultured in various culture media showed that the ability of transferrin to support tooth morphogenesis correlated with a stimulation of growth. The results support our earlier suggestions that transferrin functions as a fetal growth factor. The availability of the transferrin-containing chemically defined medium facilitates studies on the roles of other growth factors during tooth development.

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Year:  1984        PMID: 6381199     DOI: 10.1111/j.1432-0436.1984.tb01408.x

Source DB:  PubMed          Journal:  Differentiation        ISSN: 0301-4681            Impact factor:   3.880


  8 in total

1.  Morphometric analysis of the developing murine molar tooth in vivo and in vitro.

Authors:  A K Jowett; M W Ferguson
Journal:  J Anat       Date:  1991-08       Impact factor: 2.610

2.  Species specificity of transferrin binding, endocytosis and iron internalization by cultured chick myogenic cells.

Authors:  L M Sorokin; E H Morgan
Journal:  J Comp Physiol B       Date:  1988       Impact factor: 2.200

3.  Sialylation of terminal saccharides of glycoconjugates expressed by murine molar tooth germs developing in vitro and in vivo.

Authors:  A K Jowett; S J Kimber; M W Ferguson
Journal:  J Anat       Date:  1994-08       Impact factor: 2.610

4.  Immunocytochemical demonstration of nerve growth factor receptor (NGF-R) in developing human fetal teeth.

Authors:  L R Christensen; K Møllgård; I Kjaer; M S Janas
Journal:  Anat Embryol (Berl)       Date:  1993-09

5.  Transferrin and iron requirements of embryonic mesoderm cells cultured in hydrated collagen matrices.

Authors:  E J Sanders; E Cheung
Journal:  In Vitro Cell Dev Biol       Date:  1988-06

6.  Cell proliferation, extracellular matrix mineralization, and ovotransferrin transient expression during in vitro differentiation of chick hypertrophic chondrocytes into osteoblast-like cells.

Authors:  C Gentili; P Bianco; M Neri; M Malpeli; G Campanile; P Castagnola; R Cancedda; F D Cancedda
Journal:  J Cell Biol       Date:  1993-08       Impact factor: 10.539

7.  Transferrin promotes endothelial cell migration and invasion: implication in cartilage neovascularization.

Authors:  M F Carlevaro; A Albini; D Ribatti; C Gentili; R Benelli; S Cermelli; R Cancedda; F D Cancedda
Journal:  J Cell Biol       Date:  1997-03-24       Impact factor: 10.539

8.  Ovotransferrin and ovotransferrin receptor expression during chondrogenesis and endochondral bone formation in developing chick embryo.

Authors:  C Gentili; R Doliana; P Bet; G Campanile; A Colombatti; F D Cancedda; R Cancedda
Journal:  J Cell Biol       Date:  1994-02       Impact factor: 10.539

  8 in total

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