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Sci Rep ; 5: 14479, 2015 Sep 28.
Artículo en Inglés | MEDLINE | ID: mdl-26411543

RESUMEN

In common with most mammals, humans form only two dentitions during their lifetime. Occasionally, supernumerary teeth develop in addition to the normal complement. Odontoma represent a small group of malformations containing calcified dental tissues of both epithelial and mesenchymal origin, with varying levels of organization, including tooth-like structures. The specific cell type responsible for the induction of odontoma, which retains the capacity to re-initiate de novo tooth development in postnatal tissues, is not known. Here we demonstrate that aberrant activation of WNT signaling by expression of a non-degradable form of ß-catenin specifically in SOX2-positive postnatal dental epithelial stem cells is sufficient to generate odontoma containing multiple tooth-like structures complete with all dental tissue layers. Genetic lineage-tracing confirms that odontoma form in a similar manner to normal teeth, derived from both the mutation-sustaining epithelial stem cells and adjacent mesenchymal tissues. Activation of the WNT pathway in embryonic SOX2-positive progenitors results in ectopic expression of secreted signals that promote odontogenesis throughout the oral cavity. Significantly, the inductive potential of epithelial dental stem cells is retained in postnatal tissues, and up-regulation of WNT signaling specifically in these cells is sufficient to promote generation and growth of ectopic malformations faithfully resembling human odontoma.


Asunto(s)
Transformación Celular Neoplásica/metabolismo , Odontoma/metabolismo , Factores de Transcripción SOXB1/metabolismo , Células Madre/metabolismo , Vía de Señalización Wnt , Animales , Diferenciación Celular , Transformación Celular Neoplásica/genética , Células Madre Embrionarias/metabolismo , Femenino , Expresión Génica , Masculino , Ratones , Odontogénesis/genética , Odontoma/genética , Odontoma/patología , Embarazo , Factores de Transcripción SOXB1/genética , Proteínas Wnt/genética , Proteínas Wnt/metabolismo , beta Catenina/metabolismo
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