Multiple families of signaling molecules, including BMP, FGF, Shh, and Wnt protein, have been implicated in mediating tissue interactions that govern tooth development. Despite significant progresses in the last two decades since BMP4 was identified as a potential morphogen in during tooth initiation, functional mechanisms of these signaling pathways and how they act coordinately to regulate tooth formation remain elusive. Our long-term goal to delineate the molecular mechanisms underlying odontogenesis, which shall shed light on for better understanding of genetic related dental abnormalities and tooth regeneration in humans. Based on our previous and preliminary studies, we hypothesize that BMP and Wnt signaling pathways exert distinct but synergistic functions in controlling dental epithelium development, with Wnt/b- catenin signaling regulating odontogenic fate and BMP-mediated non-canonical signaling regulating cell proliferation, while Smad4-independent canonical BMP signaling (named as atypical canonical BMP signaling) acting in the dental mesenchyme to control odontogenic program by regulating Msx1 expression.
Two aims are proposed to test this hypothesis.
In Aim 1, we will several unique transgenic/knockout mouse lines dissect distinct and synergistic biological functions of Wnt- and BMP-mediated signaling pathways in the regulation of early tooth development. In this aim, we will: (1) Establish a novel function for Noggin as a Wnt signaling antagonist;(2) Establish BMP signaling as a major regulator for cell proliferation but not for odontogenic fate in the dental epithelium;(3) Define synergistic function of BMP and Wnt signaling in early tooth development;(4) Establish definite signaling function for ?-catenin in tooth development.
In Aim 2, we will use several transgenic/knockout mouse line combined with cell culture, biochemistry, and molecular biology approaches to investigate the role and regulation of atypical canonical BMP signaling in the dental mesenchyme. In this aim, we will;(1) Establish that TGFb signaling is primarily responsible for Smad1/5/8 activation in the dental epithelium;(2) Determine functional operation of atypical canonical BMP signaling in the dental mesenchyme;and (3) Investigate regulatory mechanism of atypical canonical BMP signaling in the dental mesenchyme. Results from these proposed studies will greatly enhance our understanding of functional mechanisms of BMP and Wnt signaling in tooth development and challenge the current model of the canonical BMP signaling.

Public Health Relevance

Nearly 20% of the US population has congenitally missing teeth and the probability of tooth loss increases with a person's age. The pressing demand for replacement teeth in regenerative dental medicine has brought up a matter of great urgency to explore the molecular mechanisms that regulate tooth development. This proposal studies the role of BMP and Wnt signaling during early tooth development. The proposed studies utilize a combination of genetic, experimental embryology, biochemistry, and molecular biology approaches to address the developmental function and regulation of BMP and Wnt signaling pathways in early odontogenesis. Given the considerable homology between mouse and human odontogenesis as well as the profiles of gene expression, unveiling the molecular basis involved in mouse tooth morphogenesis will provide important insight for studying genetic related dental abnormalities and tooth regeneration in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
1R01DE024152-01
Application #
8665086
Study Section
Skeletal Biology Development and Disease Study Section (SBDD)
Program Officer
Scholnick, Steven
Project Start
2014-08-01
Project End
2019-07-31
Budget Start
2014-08-01
Budget End
2015-07-31
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Tulane University
Department
Anatomy/Cell Biology
Type
Schools of Arts and Sciences
DUNS #
City
New Orleans
State
LA
Country
United States
Zip Code
70118
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