The field of salivary gland biology and regeneration is severely hampered by a lack of knowledge regarding the identification of stem or progenitor cells and the fate of this population following salivary gland damage. The cell label retaining approach can objectively identify long living and non-proliferative cells that are hypothesized to be stem and/or progenitor cells. This proposal will utilize the label retaining cell (LRC) techniqu within two established models of salivary gland restoration, post-radiation injections of insulin-like growth factor (IGF1) [3] and ductal ligation/deligation [4], in order to create a more universl understanding of salivary gland regeneration following injury. The central hypothesis of this proposal is label retaining cells play an important role in orchestrating salivary gland regeneration through reestablishment of apical- basal polarity.
Specific Aim 1 will demonstrate the regenerative potential of salivary BrdU label retaining cells (LRC).
Specific Aim 2 will evaluate the intrinsic role of apical-basal polarity within label retaining cells in restoration of cellular differentiation.
Specific Aim 3 will determine the non-cell autonomous effect of loss of polarity on the compensatory proliferation response of label retaining cells. The general goal of this proposal is to identify the capacity of label retaining cells to regenerate differentiated salivary gland structures, and to identify the role of polarity signaling mechanism in promoting differentiation and functional reconstitution. The long-term goal of this proposal is to evaluate whether novel therapies that promote apical-basal polarity within salivary stem/progenitor cells and their respective niches could improve clinical therapeutics for chronic salivary gland dysfunction and xerostomia following radiation therapy for head and neck cancer.

Public Health Relevance

Radiation is a common treatment in most head and neck cancer cases and results in the loss of saliva in most patients. The resulting lack of salivary gland activity results in significant adverse side effects, which diminish the effectiveness of ant-cancer therapies, and decreases the quality of life for these patients. The long-term goal of this proposal is to develop an effective therapeutic approach to restore salivary function. The studies could have the potential to restore salivary gland function to patients with chronic dry mouth.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
1R01DE023534-01A1
Application #
8716379
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Melillo, Amanda A
Project Start
2014-04-01
Project End
2018-12-31
Budget Start
2014-04-01
Budget End
2014-12-31
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Arizona
Department
Nutrition
Type
Earth Sciences/Resources
DUNS #
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Morgan-Bathke, M; Lin, H H; Ann, D K et al. (2015) The Role of Autophagy in Salivary Gland Homeostasis and Stress Responses. J Dent Res 94:1035-40
Chibly, Alejandro Martinez; Nguyen, Thao; Limesand, Kirsten H (2014) Palliative Care for Salivary Gland Dysfunction Highlights the Need for Regenerative Therapies: A Review on Radiation and Salivary Gland Stem Cells. J Palliat Care Med 4:
Chibly, Alejandro M; Querin, Lauren; Harris, Zoey et al. (2014) Label-retaining cells in the adult murine salivary glands possess characteristics of adult progenitor cells. PLoS One 9:e107893