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Post-natal effect of overexpressed DKK1 on mandibular molar formation
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نویسنده
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han x.l. ,liu m. ,voisey a. ,ren y.s. ,kurimoto p. ,gao t. ,tefera l. ,dechow p. ,ke h.z. ,feng j.q.
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منبع
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journal of dental research - 2011 - دوره : 90 - شماره : 11 - صفحه:1312 -1317
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چکیده
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Dickkopf-related protein 1 (dkk1) is a potent inhibitor of wnt/β-catenin signaling. dkk1-null mutant embryos display severe defects in head induction. conversely,targeted expression of dkk1 in dental epithelial cells leads to the formation of dysfunctional enamel knots and subsequent tooth defects during embryonic development. however,its role in post-natal dentinogenesis is largely unknown. to address this issue,we studied the role of dkk1 in post-natal dentin development using 2.3-kb col1a1-dkk1 transgenic mice,with the following key findings: (1) the dkk1 transgene was highly expressed in pulp and odontoblast cells during post-natal developmental stages; (2) the 1st molar displayed short roots,an enlarged pulp/root canal region,and a decrease in the dentin formation rate; (3) a small malformed second molar and an absent third molar; (4) an increase of immature odontoblasts,few mature odontoblasts,and sharply reduced dentinal tubules; and (5) a dramatic change in osx and nestin expression. we propose that dkk1 controls post-natal mandibular molar dentin formation either directly or indirectly via the inhibition of wnt signaling at the following aspects: (i) post-natal dentin formation,(ii) formation and/or maintenance of the dentin tubular system,(iii) mineralization of the dentin,and (iv) regulation of molecules such as osx and nestin. © 2011 international & american associations for dental research.
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کلیدواژه
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dentinogenesis; DKK1; mandibular molar; odontoblast; tooth development; transgenic mice
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آدرس
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baylor college of dentistry,department of biomedical sciences,texas aandm health science center,3302 gaston avenue,dallas,tx 75246,united states,state key laboratory of oral diseases,west china stomatology hospital,sichuan university,chengdu,sichuan, China, department of metabolic disorders,amgen inc.,thousand oaks,ca, United States, baylor college of dentistry,department of biomedical sciences,texas aandm health science center,3302 gaston avenue,dallas,tx 75246, United States, baylor college of dentistry,department of biomedical sciences,texas aandm health science center,3302 gaston avenue,dallas,tx 75246, United States, department of metabolic disorders,amgen inc.,thousand oaks,ca, United States, baylor college of dentistry,department of biomedical sciences,texas aandm health science center,3302 gaston avenue,dallas,tx 75246, United States, baylor college of dentistry,department of biomedical sciences,texas aandm health science center,3302 gaston avenue,dallas,tx 75246, United States, baylor college of dentistry,department of biomedical sciences,texas aandm health science center,3302 gaston avenue,dallas,tx 75246, United States, department of metabolic disorders,amgen inc.,thousand oaks,ca, United States, baylor college of dentistry,department of biomedical sciences,texas aandm health science center,3302 gaston avenue,dallas,tx 75246, United States
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Authors
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