Sox2 marks epithelial competence to generate teeth in mammals and reptiles

Author:

Juuri Emma1,Jussila Maria1,Seidel Kerstin2,Holmes Scott3,Wu Ping4,Richman Joy3,Heikinheimo Kristiina5,Chuong Cheng-Ming4,Arnold Katrin678,Hochedlinger Konrad678,Klein Ophir2,Michon Frederic1,Thesleff Irma1

Affiliation:

1. Institute of Biotechnology, Developmental Biology Program, University of Helsinki, 00014 Helsinki, Finland.

2. Departments of Orofacial Sciences and Pediatrics and Program in Craniofacial and Mesenchymal Biology, UCSF, San Francisco, CA 94143-0442, USA.

3. Life Sciences Institute, Department of Oral Health Sciences, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.

4. Department of Pathology, University of Southern California, Los Angeles, CA 90033, USA.

5. Department of Oral and Maxillofacial Surgery, Institute of Dentistry, University of Turku and Turku University Hospital, 20014, Turku, Finland.

6. Howard Hughes Medical Institute and Department of Stem Cell and Regenerative Biology, Harvard University and Harvard Medical School, Cambridge, MA 02138, USA.

7. General Hospital Cancer Center and Center for Regenerative Medicine, Boston, MA 02114, USA.

8. Harvard Stem Cell Institute, Cambridge, MA 02138, USA.

Abstract

Tooth renewal is initiated from epithelium associated with existing teeth. The development of new teeth requires dental epithelial cells that have competence for tooth formation, but specific marker genes for these cells have not been identified. Here, we analyzed expression patterns of the transcription factor Sox2 in two different modes of successional tooth formation: tooth replacement and serial addition of primary teeth. We observed specific Sox2 expression in the dental lamina that gives rise to successional teeth in mammals with one round of tooth replacement as well as in reptiles with continuous tooth replacement. Sox2 was also expressed in the dental lamina during serial addition of mammalian molars, and genetic lineage tracing indicated that Sox2+ cells of the first molar give rise to the epithelial cell lineages of the second and third molars. Moreover, conditional deletion of Sox2 resulted in hyperplastic epithelium in the forming posterior molars. Our results indicate that the Sox2+ dental epithelium has competence for successional tooth formation and that Sox2 regulates the progenitor state of dental epithelial cells. The findings imply that the function of Sox2 has been conserved during evolution and that tooth replacement and serial addition of primary teeth represent variations of the same developmental process. The expression patterns of Sox2 support the hypothesis that dormant capacity for continuous tooth renewal exists in mammals.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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