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   <subfield code="a">Combined effect of fluoride and 2,3,7,8-tetrachlorodibenzo- p -dioxin on mouse dental hard tissue formation in vitro</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Eija Salmela, Pirjo-Liisa Lukinmaa, Anna-Maija Partanen, Carin Sahlberg, Satu Alaluusua]</subfield>
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   <subfield code="a">Fluoride interferes with enamel matrix secretion and mineralization and dentin mineralization. The most toxic dioxin congener, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), also impairs dental hard tissue formation and mineralization in vitro and in vivo. Our aim was to investigate in vitro whether the combined effect of sodium fluoride (NaF) and TCDD on dental hard tissue formation is potentiative. For this purpose, mandibular first and second molar tooth germs of E18 mouse embryos were cultured for 5-12days with NaF and TCDD alone at various concentrations (2.5, 5, 10, 12.5, 15, and 20μM and 5, 10, 12.5, and 15nM, respectively) to determine the highest concentrations, which alone cause no or negligible effects. Morphological changes were studied from the whole tooth photographs and histological tissue sections. The concentrations found were 15μM for NaF and 10nM for TCDD. While at these concentrations, the effects of NaF and TCDD alone were barely detectable, the effect of simultaneous exposure on dentin and enamel formation was overt; mineralization of predentin to dentin and enamel matrix secretion and mineralization were impaired. Immunohistochemical analysis revealed that the combined exposure modified amelogenin expression by odontoblasts. Morphology of ameloblasts and the expression of amelogenin indicated that ameloblasts were still secretory. The results show that NaF and TCDD have potentiative, harmful effects on the formation of dental hard tissues. Since children can be exposed to subclinical levels of fluoride and dioxins during early childhood, coincidently with mineralization of the first permanent teeth, this finding may have clinical significance.</subfield>
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   <subfield code="a">Amelogenesis</subfield>
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   <subfield code="a">Dentinogenesis</subfield>
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   <subfield code="a">Fluoride</subfield>
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   <subfield code="u">Department of Pediatric and Preventive Dentistry, Institute of Dentistry, University of Helsinki, P.O. Box 41, 00014, Helsinki, Finland</subfield>
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   <subfield code="u">Department of Oral Pathology, Institute of Dentistry, University of Helsinki, P.O. Box 41, 00014, Helsinki, Finland</subfield>
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   <subfield code="a">Partanen</subfield>
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   <subfield code="u">Department of Pediatric and Preventive Dentistry, Institute of Dentistry, University of Helsinki, P.O. Box 41, 00014, Helsinki, Finland</subfield>
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   <subfield code="a">Sahlberg</subfield>
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   <subfield code="u">Department of Pediatric and Preventive Dentistry, Institute of Dentistry, University of Helsinki, P.O. Box 41, 00014, Helsinki, Finland</subfield>
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   <subfield code="u">Department of Pediatric and Preventive Dentistry, Institute of Dentistry, University of Helsinki, P.O. Box 41, 00014, Helsinki, Finland</subfield>
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