PERP regulates enamel formation via effects on cell–cell adhesion and gene expression

Author:

Jheon Andrew H.1,Mostowfi Pasha1,Snead Malcolm L.2,Ihrie Rebecca A.3,Sone Eli4,Pramparo Tiziano5,Attardi Laura D.6,Klein Ophir D.15

Affiliation:

1. Department of Orofacial Sciences and Program in Craniofacial and Mesenchymal Biology, University of California, San Francisco, CA 94143, USA

2. Center for Craniofacial Molecular Biology, University of Southern California, 2250 Alcazar Street – CSA 103, Los Angeles, CA 90033, USA

3. Department of Neurological Surgery and Institute for Regeneration Medicine, University of California, San Francisco, 35 Medical Center Way, RMB933, San Francisco, CA 94143-0525, USA

4. Faculty of Dentistry, Department of Materials Science and Engineering, and Institute of Biomaterials and Biomedical Engineering, University of Toronto, M5S 3G9, Canada

5. Department of Pediatrics and Institute for Human Genetics, University of California, San Francisco, CA 94143, USA

6. Departments of Radiation Oncology and Genetics, Stanford University, Palo Alto, CA 94305-5101, USA

Abstract

Little is known about the role of cell–cell adhesion in the development of mineralized tissues. Here we report that PERP, a tetraspan membrane protein essential for epithelial integrity, regulates enamel formation. PERP is necessary for proper cell attachment and gene expression during tooth development, and its expression is controlled by P63, a master regulator of stratified epithelial development. During enamel formation, PERP is localized to the interface between the enamel-producing ameloblasts and the stratum intermedium (SI), a layer of cells subjacent to the ameloblasts. Perp-null mice display dramatic enamel defects, which are caused, in part, by the detachment of ameloblasts from the SI. Microarray analysis comparing gene expression in teeth of wild-type and Perp-null mice identified several differentially expressed genes during enamel formation. Analysis of these genes in ameloblast-derived LS8 cells upon knockdown of PERP confirmed the role for PERP in the regulation of gene expression. Together, our data show that PERP is necessary for the integrity of the ameloblast–SI interface and that a lack of Perp causes downregulation of genes that are required for proper enamel formation.

Publisher

The Company of Biologists

Subject

Cell Biology

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