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   <subfield code="a">10.1007/s11626-009-9265-7</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s11626-009-9265-7</subfield>
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   <subfield code="a">Newly established cell lines from mouse oral epithelium regenerate teeth when combined with dental mesenchyme</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Chiho Takahashi, Hiroyuki Yoshida, Akihiko Komine, Kazuhisa Nakao, Takashi Tsuji, Yasuhiro Tomooka]</subfield>
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   <subfield code="a">The present study attempted to examine whether clonal cell lines of the oral epithelium can differentiate into ameloblasts and regenerate tooth when combined with dental germ mesenchyme. Clonal cell lines with a distinct morphology were established from the oral epithelium of p53-deficient fetal mice at embryonic day18 (E18). The strain of mouse is shown to be a useful source for establishing clonal and immortalized cell lines from various tissues and at various stages of development. Tooth morphogenesis is almost completed and the oral epithelium is segregated from the dental epithelium at E18. In RT-PCR analysis of cell lines, mucosal epithelial markers (cytokeratin 14) were detected, but ameloblast markers such as amelogenin and ameloblastin were not detected when cells were cultured on plastic dish. They formed stratified epithelia and expressed a specific differentiation marker (CK13) in the upper layer when cultured on feeder layer or on collagen gel for 1-3wk, demonstrating that they are of oral mucosa origin. Next, bioengineered tooth germs were prepared with cell lines and fetal molar mesenchymal tissues and implanted under kidney capsule for 2-3wk. Five among six cell lines regenerated calcified structures as seen in natural tooth. Our results indicate that some oral epithelial cells at E18 possess the capability to differentiate into ameloblasts. Furthermore, cell lines established in the present study are useful models to study processes in tooth organogenesis and tooth regeneration.</subfield>
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   <subfield code="a">The Author(s), 2009</subfield>
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   <subfield code="a">Oral epithelium</subfield>
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   <subfield code="a">Immortalized cell lines</subfield>
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   <subfield code="a">Tooth regeneration</subfield>
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   <subfield code="a">Takahashi</subfield>
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   <subfield code="u">Department of Biological Science and Technology and Tissue Engineering Research Center, Tokyo University of Science, Yamazaki 2641, 278-8510, Noda, Chiba, Japan</subfield>
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   <subfield code="a">Yoshida</subfield>
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   <subfield code="u">Department of Biological Science and Technology and Tissue Engineering Research Center, Tokyo University of Science, Yamazaki 2641, 278-8510, Noda, Chiba, Japan</subfield>
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   <subfield code="a">Komine</subfield>
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   <subfield code="u">Department of Biological Science and Technology and Tissue Engineering Research Center, Tokyo University of Science, Yamazaki 2641, 278-8510, Noda, Chiba, Japan</subfield>
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   <subfield code="a">Nakao</subfield>
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   <subfield code="u">Department of Biological Science and Technology and Tissue Engineering Research Center, Tokyo University of Science, Yamazaki 2641, 278-8510, Noda, Chiba, Japan</subfield>
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   <subfield code="a">Tsuji</subfield>
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   <subfield code="u">Department of Biological Science and Technology and Tissue Engineering Research Center, Tokyo University of Science, Yamazaki 2641, 278-8510, Noda, Chiba, Japan</subfield>
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   <subfield code="t">In Vitro Cellular &amp; Developmental Biology - Animal</subfield>
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   <subfield code="g">46/5(2010-05-01), 457-468</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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